K. Ohtsubo and J. D. Marth, Glycosylation in cellular mechanisms of health and disease, Cell, vol.126, pp.855-67, 2006.

J. W. Dennis, S. Laferte, C. Waghorne, M. L. Breitman, and R. S. Kerbel, Beta 1-6 branching of Asn-linked oligosaccharides is directly associated with metastasis, Science, vol.236, pp.582-587, 1987.

W. Chaney, S. Sundaram, N. Friedman, and P. Stanley, The Lec4A CHO glycosylation mutant arises from miscompartmentalization of a Golgi glycosyltransferase, J Cell Biol, vol.109, pp.2089-96, 1989.

K. S. Lau and J. W. Dennis, N-Glycans in cancer progression, Glycobiology, vol.18, pp.750-60, 2008.

M. Shoreibah, G. S. Perng, B. Adler, J. Weinstein, R. Basu et al., Isolation, characterization, and expression of a cDNA encoding N-acetylglucosaminyltransferase V, J Biol Chem, vol.268, pp.15381-15386, 1993.

H. Yamamoto, J. Swoger, S. Greene, T. Saito, J. Hurh et al., acetylglucosamine-bearing N-glycans in human gliomas: implications for a role in regulating invasivity, vol.60, pp.134-176, 2000.

A. A. Padhiar, J. Fan, Y. Tang, J. Yu, S. Wang et al., Upregulated beta1-6 branch N-glycan marks early gliomagenesis but exhibited biphasic expression in the progression of astrocytic glioma, Am J Cancer Res, vol.5, pp.1101-1117, 2015.

D. T. Ross, U. Scherf, M. B. Eisen, C. M. Perou, C. Rees et al., Systematic variation in gene expression patterns in human cancer cell lines, Nat Genet, vol.24, pp.227-262, 2000.

J. Gu and N. Taniguchi, Potential of N-glycan in cell adhesion and migration as either a positive or negative regulator, Cell Adh Migr, vol.2, pp.243-248, 2008.

P. O. Guichet, I. Bieche, M. Teigell, C. Serguera, B. Rothhut et al., Cell death and neuronal differentiation of glioblastoma stem-like cells induced by neurogenic transcription factors, Glia, vol.61, pp.225-264, 2013.

P. C. Burger, P. J. Dubois, S. C. Schold, J. Smith, K. R. et al., Computerized tomographic and pathologic studies of the untreated, quiescent, and recurrent glioblastoma multiforme, J Neurosurg, vol.58, pp.159-69, 1983.

J. N. Contessa, M. S. Bhojani, H. H. Freeze, A. Rehemtulla, and T. S. Lawrence, Inhibition of N-linked glycosylation disrupts receptor tyrosine kinase signaling in tumor cells, Cancer Res, vol.68, pp.3803-3812, 2008.

J. E. Hudak and C. R. Bertozzi, Glycotherapy: new advances inspire a reemergence of glycans in medicine, Chem Biol, vol.21, pp.16-37, 2014.

M. Granovsky, J. Fata, J. Pawling, W. J. Muller, R. Khokha et al., Suppression of tumor growth and metastasis in Mgat5-deficient mice, Nat Med, vol.6, pp.306-318, 2000.

J. K. Lee, R. T. Matthews, J. M. Lim, K. Swanier, L. Wells et al., Developmental expression of the neuron-specific N-acetylglucosaminyltransferase Vb (GnT-Vb/IX) and identification of its in vivo glycan products in comparison with those of its paralog, GnT-V, J Biol Chem, vol.287, pp.28526-28562, 2012.

L. Clarion, C. Jacquard, O. Sainte-catherine, M. Decoux, S. Loiseau et al., C-glycoside mimetics inhibit glioma stem cell proliferation, migration, and invasion, J Med Chem, vol.57, pp.8293-306, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01100620

L. Clarion, C. Jacquard, O. Sainte-catherine, S. Loiseau, D. Filippini et al., Oxaphosphinanes: new therapeutic perspectives for glioblastoma, J Med Chem, vol.55, pp.2196-211, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00677707

C. Dromard, H. Guillon, V. Rigau, C. Ripoll, J. C. Sabourin et al., Adult human spinal cord harbors neural precursor cells that generate neurons and glial cells in vitro, J Neurosci Res, vol.86, pp.1916-1942, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02156283

N. Aceto, A. Bardia, D. T. Miyamoto, M. C. Donaldson, B. S. Wittner et al., Circulating tumor cell clusters are oligoclonal precursors of breast cancer metastasis, Cell, vol.158, pp.1110-1122, 2014.

M. Akhmanova, E. Osidak, S. Domogatsky, S. Rodin, and A. Domogatskaya, Physical, Spatial, and Molecular Aspects of Extracellular Matrix of In Vivo Niches and Artificial Scaffolds Relevant to Stem Cells Research, Stem Cells Int, p.167025, 2015.

P. Atherton, B. Stutchbury, D. Y. Wang, D. Jethwa, R. Tsang et al., Vinculin controls talin engagement with the actomyosin machinery, Nat Commun, vol.6, 2015.

R. Babouri, M. Rolland, O. Sainte-catherine, Z. Kabouche, M. Lecouvey et al., alpha-Halogenated oxaphosphinanes: Synthesis, unexpected reactions and evaluation as inhibitors of cancer cell proliferation, Eur J Med Chem, vol.104, pp.33-41, 2015.

C. Beadle, M. C. Assanah, P. Monzo, R. Vallee, S. S. Rosenfeld et al., The role of myosin II in glioma invasion of the brain, Mol Biol Cell, vol.19, pp.3357-3368, 2008.

A. Beliveau, G. Thomas, J. Gong, Q. Wen, and A. Jain, Aligned Nanotopography Promotes a Migratory State in Glioblastoma Multiforme Tumor Cells, Sci Rep, vol.6, 2016.

A. M. Belkin and M. A. Stepp, Integrins as receptors for laminins, Microsc Res Tech, vol.51, pp.280-301, 2000.

A. F. Blandin, G. Renner, M. Lehmann, I. Lelong-rebel, S. Martin et al., beta1 Integrins as Therapeutic Targets to Disrupt Hallmarks of Cancer, Front Pharmacol, vol.6, p.279, 2015.

V. A. Cuddapah, S. Robel, S. Watkins, and H. Sontheimer, A neurocentric perspective on glioma invasion, Nat Rev Neurosci, vol.15, pp.455-465, 2014.

M. Das, S. Subbayya-ithychanda, J. Qin, and E. F. Plow, Mechanisms of talin-dependent integrin signaling and crosstalk, Biochim Biophys Acta, vol.1838, pp.579-588, 2014.

C. Dromard, H. Guillon, V. Rigau, C. Ripoll, J. C. Sabourin et al., Adult human spinal cord harbors neural precursor cells that generate neurons and glial cells in vitro, J Neurosci Res, vol.86, pp.1916-1926, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02156283

R. Filipovic, S. Santhosh-kumar, C. Fiondella, and J. Loturco, Increasing doublecortin expression promotes migration of human embryonic stem cell-derived neurons, Stem Cells, vol.30, pp.1852-1862, 2012.

S. I. Fraley, Y. Feng, R. Krishnamurthy, D. H. Kim, A. Celedon et al.,

, A distinctive role for focal adhesion proteins in three-dimensional cell motility, Nat Cell Biol, vol.12, pp.598-604

S. J. Franco, M. A. Rodgers, B. J. Perrin, J. Han, D. A. Bennin et al., Calpain-mediated proteolysis of talin regulates adhesion dynamics, Nat Cell Biol, vol.6, pp.977-983, 2004.

P. Friedl, A. , and S. , Cancer invasion and the microenvironment: plasticity and reciprocity, Cell, vol.147, pp.992-1009, 2011.

P. Friedl, J. Locker, E. Sahai, and J. E. Segall, Classifying collective cancer cell invasion, Nat Cell Biol, vol.14, pp.777-783, 2012.

A. Glading, D. A. Lauffenburger, and A. Wells, Cutting to the chase: calpain proteases in cell motility, Trends Cell Biol, vol.12, pp.46-54, 2002.

J. G. Goetz, B. Joshi, P. Lajoie, S. S. Strugnell, T. Scudamore et al., Concerted regulation of focal adhesion dynamics by galectin-3 and tyrosine, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00285445

, J Cell Biol, vol.180, pp.1261-1275

P. G. Gritsenko, O. Ilina, and P. Friedl, Interstitial guidance of cancer invasion, J Pathol, vol.226, pp.185-199, 2012.

P. O. Guichet, I. Bieche, M. Teigell, C. Serguera, B. Rothhut et al., Cell death and neuronal differentiation of glioblastoma stem-like cells induced by neurogenic transcription factors, Glia, vol.61, pp.225-239, 2013.

M. Herrera-perez, S. L. Voytik-harbin, and J. L. Rickus, Extracellular Matrix Properties Regulate the Migratory Response of Glioblastoma Stem Cells in Three-Dimensional Culture, Tissue Eng Part A, vol.21, pp.2572-2582, 2015.

E. R. Horton, A. Byron, J. A. Askari, D. H. Ng, A. Millon-fremillon et al., Definition of a consensus integrin adhesome and its dynamics during adhesion complex assembly and disassembly, Nat Cell Biol, vol.17, pp.1577-1587, 2015.

R. C. Hughes, Galectins as modulators of cell adhesion, Biochimie, vol.83, pp.667-676, 2001.

R. O. Hynes, Integrins: bidirectional, allosteric signaling machines, Cell, vol.110, pp.673-687, 2002.

H. S. Jang, S. Lal, and J. A. Greenwood, Calpain 2 is required for glioblastoma cell invasion: regulation of matrix metalloproteinase 2, Neurochem Res, vol.35, pp.1796-1804, 2010.

K. Kallenberg, T. Goldmann, J. Menke, H. Strik, H. C. Bock et al., Glioma infiltration of the corpus callosum: early signs detected by DTI, J Neurooncol, vol.112, pp.217-222, 2013.

S. Lal, J. La-du, R. L. Tanguay, and J. A. Greenwood, Calpain 2 is required for the invasion of glioblastoma cells in the zebrafish brain microenvironment, J Neurosci Res, vol.90, pp.769-781, 2012.

J. D. Lathia, J. Gallagher, J. M. Heddleston, J. Wang, C. E. Eyler et al., Integrin alpha 6 regulates glioblastoma stem cells, Cell Stem Cell, vol.6, pp.421-432, 2010.

J. D. Lathia, M. Li, P. E. Hall, J. Gallagher, J. S. Hale et al., Laminin alpha 2 enables glioblastoma stem cell growth, Ann Neurol, vol.72, pp.766-778, 2012.

D. A. Lauffenburger and A. F. Horwitz, Cell migration: a physically integrated molecular process, Cell, vol.84, pp.359-369, 1996.

D. Liewald, R. Miller, N. Logothetis, H. J. Wagner, and A. Schuz, Distribution of axon diameters in cortical white matter: an electron-microscopic study on three human brains and a macaque, Biol Cybern, vol.108, pp.541-557, 2014.

A. Manninen and M. Varjosalo, A proteomics view on integrin-mediated adhesions, Proteomics, vol.17, 2017.

C. T. Mierke, P. Kollmannsberger, D. P. Zitterbart, G. Diez, T. M. Koch et al., Vinculin facilitates cell invasion into three-dimensional collagen matrices, J Biol Chem, vol.285, pp.13121-13130, 2010.
DOI : 10.1074/jbc.m109.087171

URL : http://www.jbc.org/content/285/17/13121.full.pdf

H. A. Multhaupt, B. Leitinger, D. Gullberg, and J. R. Couchman, Extracellular matrix component signaling in cancer, Adv Drug Deliv Rev, vol.97, pp.28-40, 2016.
DOI : 10.1016/j.addr.2015.10.013

URL : http://spiral.imperial.ac.uk/bitstream/10044/1/28892/6/ADDR-D-15-00107R1.pdf

A. Nayal, D. J. Webb, and A. F. Horwitz, Talin: an emerging focal point of adhesion dynamics, Curr Opin Cell Biol, vol.16, pp.94-98, 2004.

L. Pan, Y. Zhao, Z. Yuan, and G. Qin, Research advances on structure and biological functions of integrins. Springerplus 5, p.1094, 2016.

J. T. Parsons, A. R. Horwitz, and M. A. Schwartz, Cell adhesion: integrating cytoskeletal dynamics and cellular tension, Nat Rev Mol Cell Biol, vol.11, pp.633-643, 2010.
DOI : 10.1038/nrm2957

URL : http://europepmc.org/articles/pmc2992881?pdf=render

M. W. Pickup, J. K. Mouw, and V. M. Weaver, The extracellular matrix modulates the hallmarks of cancer, EMBO Rep, vol.15, pp.1243-1253, 2014.

R. R. Rayavarapu, B. Heiden, N. Pagani, M. M. Shaw, S. Shuff et al., The role of multicellular aggregation in the survival of ErbB2-positive breast cancer cells during extracellular matrix detachment, J Biol Chem, vol.290, pp.8722-8733, 2015.

N. Shologu, E. Szegezdi, A. Lowery, M. Kerin, A. Pandit et al., Recreating complex pathophysiologies in vitro with extracellular matrix surrogates for anticancer therapeutics screening, Drug Discov Today, vol.21, pp.1521-1531, 2016.

B. B. Tysnes, L. F. Larsen, G. O. Ness, R. Mahesparan, K. Edvardsen et al., Stimulation of glioma-cell migration by laminin and inhibition by anti-alpha3 and anti-beta1 integrin antibodies, Int J Cancer, vol.67, pp.777-784, 1996.

S. Y. Wong and S. Kumar, Matrix regulation of tumor-initiating cells, Prog Mol Biol Transl Sci, vol.126, pp.243-256, 2014.
DOI : 10.1016/b978-0-12-394624-9.00010-5

X. Zhao and J. L. Guan, Focal adhesion kinase and its signaling pathways in cell migration and angiogenesis, Adv Drug Deliv Rev, vol.63, pp.610-615, 2011.
DOI : 10.1016/j.addr.2010.11.001

URL : http://europepmc.org/articles/pmc3132829?pdf=render

J. Zhong, J. B. Baquiran, N. Bonakdar, J. Lees, Y. W. Ching et al., NEDD9 stabilizes focal adhesions, increases binding to the extra-cellular matrix and differentially effects 2D versus 3D cell migration, PLoS One, vol.7, p.35058, 2012.

N. Aceto, A. Bardia, D. T. Miyamoto, M. C. Donaldson, B. S. Wittner et al., Circulating tumor cell clusters are oligoclonal precursors of breast cancer metastasis, Cell, vol.158, pp.1110-1122, 2014.

C. Adamson, O. O. Kanu, A. I. Mehta, C. Di, N. Lin et al., Glioblastoma multiforme: a review of where we have been and where we are going, Expert Opin Investig Drugs, vol.18, pp.1061-1083, 2009.

Q. Aftab, W. C. Sin, and C. C. Naus, Reduction in gap junction intercellular communication promotes glioma migration, Oncotarget, vol.6, pp.11447-11464, 2015.
DOI : 10.18632/oncotarget.3407

URL : http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=download&path%5B%5D=3407&path%5B%5D=9073

S. Agarwal, J. H. Wendorff, and A. Greiner, Progress in the field of electrospinning for tissue engineering applications, Adv Mater, vol.21, pp.3343-3351, 2009.

P. A. Agudelo-garcia, J. K. De-jesus, S. P. Williams, M. O. Nowicki, E. A. Chiocca et al., Glioma cell migration on threedimensional nanofiber scaffolds is regulated by substrate topography and abolished by inhibition of STAT3 signaling, Neoplasia, vol.13, pp.831-840, 2011.

M. Akhmanova, E. Osidak, S. Domogatsky, S. Rodin, and A. Domogatskaya, Physical, Spatial, and Molecular Aspects of Extracellular Matrix of In Vivo Niches and Artificial Scaffolds Relevant to Stem Cells Research, Stem Cells Int, p.167025, 2015.

B. Ananthanarayanan, Y. Kim, and S. Kumar, Elucidating the mechanobiology of malignant brain tumors using a brain matrix-mimetic hyaluronic acid hydrogel platform, Biomaterials, vol.32, pp.7913-7923, 2011.

P. W. Anderson, More is different, Science, vol.177, pp.393-396, 1972.

P. Atherton, B. Stutchbury, D. Y. Wang, D. Jethwa, R. Tsang et al., Vinculin controls talin engagement with the actomyosin machinery, Nat Commun, vol.6, 2015.

R. Babouri, M. Rolland, O. Sainte-catherine, Z. Kabouche, M. Lecouvey et al., alpha-Halogenated oxaphosphinanes: Synthesis, unexpected reactions and evaluation as inhibitors of cancer cell proliferation, Eur J Med Chem, vol.104, pp.33-41, 2015.

C. Beadle, M. C. Assanah, P. Monzo, R. Vallee, S. S. Rosenfeld et al., The role of myosin II in glioma invasion of the brain, Mol Biol Cell, vol.19, pp.3357-3368, 2008.

P. Beauchesne, Extra-neural metastases of malignant gliomas: myth or reality?, Cancers (Basel), vol.3, pp.461-477, 2011.

A. Beliveau, G. Thomas, J. Gong, Q. Wen, and A. Jain, Aligned Nanotopography Promotes a Migratory State in Glioblastoma Multiforme Tumor Cells, Sci Rep, vol.6, 2016.

A. M. Belkin and M. A. Stepp, Integrins as receptors for laminins, Microsc Res Tech, vol.51, pp.280-301, 2000.

A. C. Bellail, S. B. Hunter, D. J. Brat, C. Tan, and E. G. Van-meir, Microregional extracellular matrix heterogeneity in brain modulates glioma cell invasion, Int J Biochem Cell Biol, vol.36, pp.1046-1069, 2004.

L. Bello, M. Francolini, P. Marthyn, J. Zhang, R. S. Carroll et al., Alpha(v)beta3 and alpha(v)beta5 integrin expression in glioma periphery, Neurosurgery, vol.49, pp.380-389, 2001.

A. E. Berman, N. I. Kozlova, and G. E. Morozevich, Integrins: structure and signaling, Biochemistry (Mosc), vol.68, pp.1284-1299, 2003.

D. Bianconi, M. Unseld, and G. W. Prager, Integrins in the Spotlight of Cancer, Int J Mol Sci, vol.17, 2016.

A. F. Blandin, F. Noulet, G. Renner, M. C. Mercier, L. Choulier et al., Glioma cell dispersion is driven by alpha5 integrin-mediated cellmatrix and cell-cell interactions, Cancer Lett, vol.376, pp.328-338, 2016.

A. F. Blandin, G. Renner, M. Lehmann, I. Lelong-rebel, S. Martin et al., beta1 Integrins as Therapeutic Targets to Disrupt Hallmarks of Cancer, Front Pharmacol, vol.6, p.279, 2015.

C. Bonnans, J. Chou, and Z. Werb, Remodelling the extracellular matrix in development and disease, Nat Rev Mol Cell Biol, vol.15, pp.786-801, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01952416

D. Bonnet and J. E. Dick, Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell, Nat Med, vol.3, pp.730-737, 1997.

C. Boscher, Y. Z. Zheng, R. Lakshminarayan, L. Johannes, J. W. Dennis et al., , 2012.

, Galectin-3 protein regulates mobility of N-cadherin and GM1 ganglioside at cell-cell junctions of mammary carcinoma cells, J Biol Chem, vol.287, pp.32940-32952

D. F. Braga-malta, N. E. Reticker-flynn, C. L. Da-silva, J. M. Cabral, H. E. Fleming et al., Extracellular matrix microarrays to study inductive signaling for endoderm specification, Acta Biomater, vol.34, pp.30-40, 2016.

D. J. Brat, Glioblastoma: biology, genetics, and behavior, Am Soc Clin Oncol Educ Book, pp.102-107, 2012.

N. Brosicke, F. K. Van-landeghem, B. Scheffler, and A. Faissner, Tenascin-C is expressed by human glioma in vivo and shows a strong association with tumor blood vessels, Cell Tissue Res, vol.354, pp.409-430, 2013.

P. C. Burger, P. J. Dubois, S. C. Schold, . Jr, K. R. Smith et al., Computerized tomographic and pathologic studies of the untreated, quiescent, and recurrent glioblastoma multiforme, J Neurosurg, vol.58, pp.159-169, 1983.

J. J. Cai, Z. X. Qi, W. Hua, J. J. Zhu, X. Zhang et al., Increased expression of Capn4 is associated with the malignancy of human glioma, CNS Neurosci Ther, vol.20, pp.521-527, 2014.

M. B. Calalb, T. R. Polte, and S. K. Hanks, Tyrosine phosphorylation of focal adhesion kinase at sites in the catalytic domain regulates kinase activity: a role for Src family kinases, Mol Cell Biol, vol.15, pp.954-963, 1995.

D. A. Calderwood, Talin controls integrin activation, Biochem Soc Trans, vol.32, pp.434-437, 2004.

W. Chaney, S. Sundaram, N. Friedman, and P. Stanley, The Lec4A CHO glycosylation mutant arises from miscompartmentalization of a Golgi glycosyltransferase, J Cell Biol, vol.109, pp.2089-2096, 1989.

G. Charras and E. Sahai, Physical influences of the extracellular environment on cell migration, Nat Rev Mol Cell Biol, vol.15, pp.813-824, 2014.

Z. L. Chen, V. Haegeli, H. Yu, and S. Strickland, Cortical deficiency of laminin gamma1 impairs the AKT/GSK-3beta signaling pathway and leads to defects in neurite outgrowth and neuronal migration, Dev Biol, vol.327, pp.158-168, 2009.

B. Cheng, M. Montmasson, L. Terradot, R. , and P. , Syndecans as Cell Surface Receptors in Cancer Biology. A Focus on their Interaction with PDZ Domain Proteins, Front Pharmacol, vol.7, p.10, 2016.

D. A. Chesler, M. S. Berger, and A. Quinones-hinojosa, The potential origin of glioblastoma initiating cells, Front Biosci (Schol Ed), vol.4, pp.190-205, 2012.

C. L. Chiu, J. S. Aguilar, C. Y. Tsai, G. Wu, E. Gratton et al., Nanoimaging of focal adhesion dynamics in 3D, PLoS One, vol.9, p.99896, 2014.

D. Cho, L. Matlock-colangelo, C. Xiang, P. J. Asiello, A. J. Baeumer et al., Electrospun nanofibers for microfluidic analytical systems, Polymer, vol.52, pp.3413-3421, 2011.

A. Claes, A. J. Idema, and P. Wesseling, Diffuse glioma growth: a guerilla war, Acta Neuropathol, vol.114, pp.443-458, 2007.

L. Clarion, C. Jacquard, O. Sainte-catherine, M. Decoux, S. Loiseau et al., C-glycoside mimetics inhibit glioma stem cell proliferation, migration, and invasion, J Med Chem, vol.57, pp.8293-8306, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01100620

L. Clarion, C. Jacquard, O. Sainte-catherine, S. Loiseau, D. Filippini et al., Oxaphosphinanes: new therapeutic perspectives for glioblastoma, J Med Chem, vol.55, pp.2196-2211, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00677707

J. N. Contessa, M. S. Bhojani, H. H. Freeze, A. Rehemtulla, and T. S. Lawrence, Inhibition of N-linked glycosylation disrupts receptor tyrosine kinase signaling in tumor cells, Cancer Res, vol.68, pp.3803-3809, 2008.

N. S. Corsini and A. Martin-villalba, Integrin alpha 6: anchors away for glioma stem cells, Cell Stem Cell, vol.6, pp.403-404, 2010.

V. A. Cuddapah, S. Robel, S. Watkins, and H. Sontheimer, A neurocentric perspective on glioma invasion, Nat Rev Neurosci, vol.15, pp.455-465, 2014.

W. Daddy, Removal of right cerebral hemisphere for certain tumors with hemiplegia, JAMA, 1928.

N. De-franceschi, A. Arjonen, N. Elkhatib, K. Denessiouk, A. G. Wrobel et al., Selective integrin endocytosis is driven by interactions between the integrin alpha-chain and AP2, Nat Struct Mol Biol, vol.23, pp.172-179, 2016.

T. Demuth, J. L. Rennert, D. B. Hoelzinger, L. B. Reavie, M. Nakada et al., Glioma cells on the run -the migratory transcriptome of 10 human glioma cell lines, BMC Genomics, vol.9, p.54, 2008.

J. W. Dennis, Many Light Touches Convey the Message, Trends Biochem Sci, vol.40, pp.673-686, 2015.

J. W. Dennis, S. Laferte, C. Waghorne, M. L. Breitman, and R. S. Kerbel, Beta 1-6 branching of Asnlinked oligosaccharides is directly associated with metastasis, Science, vol.236, pp.582-585, 1987.

S. P. Desai, S. N. Bhatia, M. Toner, and D. Irimia, Mitochondrial localization and the persistent migration of epithelial cancer cells, Biophys J, vol.104, pp.2077-2088, 2013.

C. Dromard, H. Guillon, V. Rigau, C. Ripoll, J. C. Sabourin et al., Adult human spinal cord harbors neural precursor cells that generate neurons and glial cells in vitro, J Neurosci Res, vol.86, pp.1916-1926, 2008.
DOI : 10.1002/jnr.21646

URL : https://hal.archives-ouvertes.fr/inserm-00349495

H. Duffau, A new philosophy in surgery for diffuse low-grade glioma (DLGG): oncological and functional outcomes, Neurochirurgie, vol.59, pp.2-8, 2013.

H. Emonard, L. Duca, and S. Dedieu, Editorial: Matricellular Receptors As Potential Targets in AntiCancer Therapeutic Strategies, Front Pharmacol, vol.7, p.95, 2016.

N. Espitia-pinzon, B. Sanz-morello, J. J. Breve, J. G. Bol, B. Drukarch et al.,

, Astrocyte-derived tissue Transglutaminase affects fibronectin deposition, but not aggregation, during cuprizone-induced demyelination, Sci Rep, vol.7, p.40995

S. Etienne-manneville and A. Hall, Integrin-mediated activation of Cdc42 controls cell polarity in migrating astrocytes through PKCzeta, Cell, vol.106, pp.489-498, 2001.

E. Farahani, H. K. Patra, J. R. Jangamreddy, I. Rashedi, M. Kawalec et al., Cell adhesion molecules and their relation to (cancer) cell stemness, Carcinogenesis, vol.35, pp.747-759, 2014.
DOI : 10.1093/carcin/bgu045

URL : https://academic.oup.com/carcin/article-pdf/35/4/747/14133255/bgu045.pdf

G. Fernandez-fuente, P. Mollinedo, L. Grande, A. Vazquez-barquero, and J. L. Fernandez-luna, , 2014.

, Culture dimensionality influences the resistance of glioblastoma stem-like cells to multikinase inhibitors, Mol Cancer Ther, vol.13, pp.1664-1672

S. J. Florczyk, K. Wang, S. Jana, D. L. Wood, S. K. Sytsma et al., Porous chitosan-hyaluronic acid scaffolds as a mimic of glioblastoma microenvironment ECM, Biomaterials, vol.34, pp.10143-10150, 2013.

R. A. Foty, Tumor cohesion and glioblastoma cell dispersal, Future Oncol, vol.9, pp.1121-1132, 2013.
DOI : 10.2217/fon.13.66

URL : http://europepmc.org/articles/pmc3881193?pdf=render

S. I. Fraley, Y. Feng, R. Krishnamurthy, D. H. Kim, A. Celedon et al., A distinctive role for focal adhesion proteins in three-dimensional cell motility, Nat Cell Biol, vol.12, pp.598-604, 2010.

S. J. Franco, M. A. Rodgers, B. J. Perrin, J. Han, D. A. Bennin et al., , 2004.

, Calpain-mediated proteolysis of talin regulates adhesion dynamics, Nat Cell Biol, vol.6, pp.977-983

P. Friedl and D. Gilmour, Collective cell migration in morphogenesis, regeneration and cancer, Nat Rev Mol Cell Biol, vol.10, pp.445-457, 2009.
DOI : 10.1038/nrm2720

P. Friedl, J. Locker, E. Sahai, and J. E. Segall, Classifying collective cancer cell invasion, Nat Cell Biol, vol.14, pp.777-783, 2012.
DOI : 10.1038/ncb2548

P. Friedl, M. , and R. , Tuning Collective Cell Migration by Cell-Cell Junction Regulation, Cold Spring Harb Perspect Biol, vol.9, 2017.
DOI : 10.1101/cshperspect.a029199

URL : http://cshperspectives.cshlp.org/content/9/4/a029199.full.pdf

P. Friedl and K. Wolf, Tumour-cell invasion and migration: diversity and escape mechanisms, Nat Rev Cancer, vol.3, pp.362-374, 2003.
DOI : 10.1038/nrc1075

J. Friedrichs, A. Manninen, D. J. Muller, and J. Helenius, Galectin-3 regulates integrin alpha2beta1-mediated adhesion to collagen-I and -IV, J Biol Chem, vol.283, pp.32264-32272, 2008.

M. Fujita, N. M. Khazenzon, A. V. Ljubimov, B. S. Lee, I. Virtanen et al., Inhibition of laminin-8 in vivo using a novel poly(malic acid)-based carrier reduces glioma angiogenesis, Angiogenesis, vol.9, pp.183-191, 2006.

R. Galli, E. Binda, U. Orfanelli, B. Cipelletti, A. Gritti et al., Isolation and characterization of tumorigenic, stem-like neural precursors from human glioblastoma, Cancer Res, vol.64, pp.7011-7021, 2004.

M. L. Gardel, I. C. Schneider, Y. Aratyn-schaus, and C. M. Waterman, Mechanical integration of actin and adhesion dynamics in cell migration, Annu Rev Cell Dev Biol, vol.26, pp.315-333, 2010.

T. Garzon-muvdi, P. Schiapparelli, C. Ap-rhys, H. Guerrero-cazares, C. Smith et al., Regulation of brain tumor dispersal by NKCC1 through a novel role in focal adhesion regulation, PLoS Biol, vol.10, 2012.

A. Giganti and E. Friederich, The actin cytoskeleton as a therapeutic target: state of the art and future directions, Prog Cell Cycle Res, vol.5, pp.511-525, 2003.

A. Glading, D. A. Lauffenburger, and A. Wells, Cutting to the chase: calpain proteases in cell motility, Trends Cell Biol, vol.12, pp.46-54, 2002.

N. Goffart, J. Kroonen, and B. Rogister, Glioblastoma-initiating cells: relationship with neural stem cells and the micro-environment, Cancers (Basel), vol.5, pp.1049-1071, 2013.

M. Granovsky, J. Fata, J. Pawling, W. J. Muller, R. Khokha et al., Suppression of tumor growth and metastasis in Mgat5-deficient mice, Nat Med, vol.6, pp.306-312, 2000.

C. W. Greider and E. H. Blackburn, A telomeric sequence in the RNA of Tetrahymena telomerase required for telomere repeat synthesis, Nature, vol.337, pp.331-337, 1989.

P. G. Gritsenko, O. Ilina, and P. Friedl, Interstitial guidance of cancer invasion, J Pathol, vol.226, pp.185-199, 2012.

T. J. Grundy, E. De-leon, K. R. Griffin, B. W. Stringer, B. W. Day et al., Differential response of patient-derived primary glioblastoma cells to environmental stiffness, Sci Rep, vol.6, p.23353, 2016.

J. Gu and N. Taniguchi, Potential of N-glycan in cell adhesion and migration as either a positive or negative regulator, Cell Adh Migr, vol.2, pp.243-245, 2008.

X. Guan, Cancer metastases: challenges and opportunities, Acta Pharm Sin B, vol.5, pp.402-418, 2015.

P. O. Guichet, I. Bieche, M. Teigell, C. Serguera, B. Rothhut et al., Cell death and neuronal differentiation of glioblastoma stem-like cells induced by neurogenic transcription factors, Glia, 2012.

P. O. Guichet, I. Bieche, M. Teigell, C. Serguera, B. Rothhut et al., Cell death and neuronal differentiation of glioblastoma stem-like cells induced by neurogenic transcription factors, Glia, vol.61, pp.225-239, 2013.

P. Guo, Q. Y. Wang, H. B. Guo, Z. H. Shen, and H. L. Chen, N-acetylglucosaminyltransferase V modifies the signaling pathway of epidermal growth factor receptor, Cell Mol Life Sci, vol.61, pp.1795-1804, 2004.

A. W. Haining, T. J. Lieberthal, D. R. Hernandez, and A. , Talin: a mechanosensitive molecule in health and disease, FASEB J, vol.30, pp.2073-2085, 2016.

D. Hambardzumyan and G. Bergers, Glioblastoma: Defining Tumor Niches, Trends Cancer, vol.1, pp.252-265, 2015.

J. Han, C. A. Alvarez-breckenridge, Q. E. Wang, Y. , and J. , TGF-beta signaling and its targeting for glioma treatment, Am J Cancer Res, vol.5, pp.945-955, 2015.

D. Hanahan and R. A. Weinberg, The hallmarks of cancer, Cell, vol.100, pp.57-70, 2000.

H. D. Hemmati, I. Nakano, J. A. Lazareff, M. Masterman-smith, D. H. Geschwind et al., Cancerous stem cells can arise from pediatric brain tumors, Proc Natl Acad Sci U S A, vol.100, pp.15178-15183, 2003.

M. Herrera-perez, S. L. Voytik-harbin, and J. L. Rickus, Extracellular Matrix Properties Regulate the Migratory Response of Glioblastoma Stem Cells in Three-Dimensional Culture, Tissue Eng Part A, vol.21, pp.2572-2582, 2015.

E. Hirata, D. Park, and E. Sahai, Retrograde flow of cadherins in collective cell migration, Nat Cell Biol, vol.16, pp.621-623, 2014.

D. B. Hoelzinger, L. Mariani, J. Weis, T. Woyke, T. J. Berens et al., Gene expression profile of glioblastoma multiforme invasive phenotype points to new therapeutic targets, Neoplasia, vol.7, pp.7-16, 2005.

E. R. Horton, A. Byron, J. A. Askari, D. H. Ng, A. Millon-fremillon et al., Definition of a consensus integrin adhesome and its dynamics during adhesion complex assembly and disassembly, Nat Cell Biol, vol.17, pp.1577-1587, 2015.

J. E. Hudak and C. R. Bertozzi, Glycotherapy: new advances inspire a reemergence of glycans in medicine, Chem Biol, vol.21, pp.16-37, 2014.

R. C. Hughes, Galectins as modulators of cell adhesion, Biochimie, vol.83, pp.667-676, 2001.

R. O. Hynes, Integrins: bidirectional, allosteric signaling machines, Cell, vol.110, pp.673-687, 2002.

T. N. Ignatova, V. G. Kukekov, E. D. Laywell, O. N. Suslov, F. D. Vrionis et al., Human cortical glial tumors contain neural stem-like cells expressing astroglial and neuronal markers in vitro, Glia, vol.39, pp.193-206, 2002.

Y. Ihara, A. Nishikawa, T. Tohma, H. Soejima, N. Niikawa et al., cDNA cloning, expression, and chromosomal localization of human N-acetylglucosaminyltransferase III (GnT-III), J Biochem, vol.113, pp.692-698, 1993.

O. Ilina and P. Friedl, Mechanisms of collective cell migration at a glance, J Cell Sci, vol.122, pp.3203-3208, 2009.

A. Ishii, T. Kimura, H. Sadahiro, H. Kawano, K. Takubo et al., Histological Characterization of the Tumorigenic "Peri-Necrotic Niche" Harboring Quiescent Stem-Like Tumor Cells in Glioblastoma, PLoS One, vol.11, 2016.

Y. Iwadate, T. Matsutani, S. Hirono, N. Shinozaki, and N. Saeki, Transforming growth factor-beta and stem cell markers are highly expressed around necrotic areas in glioblastoma, J Neurooncol, vol.129, pp.101-107, 2016.

A. Jain, M. Betancur, G. D. Patel, C. M. Valmikinathan, V. J. Mukhatyar et al., Guiding intracortical brain tumour cells to an extracortical cytotoxic hydrogel using aligned polymeric nanofibres, Nat Mater, vol.13, pp.308-316, 2014.

H. S. Jang, S. Lal, and J. A. Greenwood, Calpain 2 is required for glioblastoma cell invasion: regulation of matrix metalloproteinase 2, Neurochem Res, vol.35, pp.1796-1804, 2010.

M. E. Janik, A. Litynska, and P. Vereecken, Cell migration-the role of integrin glycosylation, Biochim Biophys Acta, vol.1800, pp.545-555, 2010.

X. Jin, The role of neurogenesis during development and in the adult brain, Eur J Neurosci, vol.44, pp.2291-2299, 2016.

J. V. Joseph, S. Conroy, K. Pavlov, P. Sontakke, T. Tomar et al., Hypoxia enhances migration and invasion in glioblastoma by promoting a mesenchymal shift mediated by the HIF1alpha-ZEB1 axis, Cancer Lett, vol.359, pp.107-116, 2015.

M. Jucker, M. Tian, and D. K. Ingram, Laminins in the adult and aged brain, Mol Chem Neuropathol, vol.28, pp.209-218, 1996.

J. P. Jung, M. K. Bache-wiig, P. P. Provenzano, and B. M. Ogle, Heterogeneous Differentiation of Human Mesenchymal Stem Cells in 3D Extracellular Matrix Composites, Biores Open Access, vol.5, pp.37-48, 2016.

N. K. Karamanos, Extracellular Matrix: Pathobiology and Signaling, 2012.

T. Kawataki, T. Yamane, H. Naganuma, P. Rousselle, I. Anduren et al., , 2007.

, Laminin isoforms and their integrin receptors in glioma cell migration and invasiveness: Evidence for a role of alpha5-laminin(s) and alpha3beta1 integrin, Exp Cell Res, vol.313, pp.3819-3831

P. J. Killela, Z. J. Reitman, Y. Jiao, C. Bettegowda, N. Agrawal et al., TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal, Proc Natl Acad Sci U S A, vol.110, pp.6021-6026, 2013.

P. J. Kim, D. Y. Lee, J. , and H. , Centralized modularity of N-linked glycosylation pathways in mammalian cells, PLoS One, vol.4, p.7317, 2009.

C. R. Kothapalli and R. D. Kamm, 3D matrix microenvironment for targeted differentiation of embryonic stem cells into neural and glial lineages, Biomaterials, vol.34, pp.5995-6007, 2013.

S. Laferte and J. W. Dennis, Glycosylation-dependent collagen-binding activities of two membrane glycoproteins in MDAY-D2 tumor cells, Cancer Res, vol.48, pp.4743-4748, 1988.

A. Lagana, J. G. Goetz, P. Cheung, A. Raz, J. W. Dennis et al., Galectin binding to Mgat5-modified N-glycans regulates fibronectin matrix remodeling in tumor cells, Mol Cell Biol, vol.26, pp.3181-3193, 2006.
URL : https://hal.archives-ouvertes.fr/hal-00129907

F. Lagarrigue, C. Kim, and M. H. Ginsberg, The Rap1-RIAM-talin axis of integrin activation and blood cell function, Blood, vol.128, pp.479-487, 2016.

S. Lal, J. La-du, R. L. Tanguay, and J. A. Greenwood, Calpain 2 is required for the invasion of glioblastoma cells in the zebrafish brain microenvironment, J Neurosci Res, vol.90, pp.769-781, 2012.

J. D. Lathia, J. Gallagher, J. M. Heddleston, J. Wang, C. E. Eyler et al., Integrin alpha 6 regulates glioblastoma stem cells, Cell Stem Cell, vol.6, pp.421-432, 2010.

J. D. Lathia, M. Li, P. E. Hall, J. Gallagher, J. S. Hale et al., Laminin alpha 2 enables glioblastoma stem cell growth, Ann Neurol, vol.72, pp.766-778, 2012.

J. D. Lathia, S. C. Mack, E. E. Mulkearns-hubert, C. L. Valentim, and J. N. Rich, Cancer stem cells in glioblastoma, Genes Dev, vol.29, pp.1203-1217, 2015.

K. S. Lau and J. W. Dennis, N-Glycans in cancer progression, Glycobiology, vol.18, pp.750-760, 2008.

K. S. Lau, E. A. Partridge, A. Grigorian, C. I. Silvescu, V. N. Reinhold et al., , 2007.

, Complex N-glycan number and degree of branching cooperate to regulate cell proliferation and differentiation, Cell, vol.129, pp.123-134

P. U. Le, A. Angers-loustau, R. M. De-oliveira, A. Ajlan, C. L. Brassard et al., DRR drives brain cancer invasion by regulating cytoskeletal-focal adhesion dynamics, Oncogene, vol.29, pp.4636-4647, 2010.

J. K. Lee, R. T. Matthews, J. M. Lim, K. Swanier, L. Wells et al., Developmental expression of the neuron-specific N-acetylglucosaminyltransferase Vb (GnT-Vb/IX) and identification of its in vivo glycan products in comparison with those of its paralog, GnT-V, J Biol Chem, vol.287, pp.28526-28536, 2012.

F. Lefranc, J. Brotchi, and R. Kiss, Possible future issues in the treatment of glioblastomas: special emphasis on cell migration and the resistance of migrating glioblastoma cells to apoptosis, J Clin Oncol, vol.23, pp.2411-2422, 2005.

K. R. Legate, S. A. Wickstrom, and R. Fassler, Genetic and cell biological analysis of integrin outside-in signaling, Genes Dev, vol.23, pp.397-418, 2009.

A. Leins, P. Riva, R. Lindstedt, M. S. Davidoff, P. Mehraein et al., Expression of tenascin-C in various human brain tumors and its relevance for survival in patients with astrocytoma, Cancer, vol.98, pp.2430-2439, 2003.

G. Lemercier, B. Espiau, F. A. Ruiz, M. Vieira, S. Luo et al., A pyrophosphatase regulating polyphosphate metabolism in acidocalcisomes is essential for Trypanosoma brucei virulence in mice, J Biol Chem, vol.279, pp.3420-3425, 2004.

D. Liewald, R. Miller, N. Logothetis, H. J. Wagner, and A. Schuz, Distribution of axon diameters in cortical white matter: an electron-microscopic study on three human brains and a macaque, Biol Cybern, vol.108, pp.541-557, 2014.

S. Loffek, C. W. Franzke, and I. Helfrich, Tension in Cancer, Int J Mol Sci, vol.17, 2016.

D. N. Louis, A. Perry, G. Reifenberger, A. Von-deimling, D. Figarella-branger et al., The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary, Acta Neuropathol, vol.131, pp.803-820, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01479018

P. Lu, V. M. Weaver, and Z. Werb, The extracellular matrix: a dynamic niche in cancer progression, J Cell Biol, vol.196, pp.395-406, 2012.

K. Ludwig and H. I. Kornblum, Molecular markers in glioma, J Neurooncol, 2017.
DOI : 10.1007/s11060-017-2379-y

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568999

A. Manninen and M. Varjosalo, A proteomics view on integrin-mediated adhesions, Proteomics, vol.17, 2017.
DOI : 10.1002/pmic.201600022

URL : http://jultika.oulu.fi/files/nbnfi-fe2019042513331.pdf

A. Martinez-gonzalez, G. F. Calvo, L. A. Perez-romasanta, and V. M. Perez-garcia, Hypoxic cell waves around necrotic cores in glioblastoma: a biomathematical model and its therapeutic implications, Bull Math Biol, vol.74, pp.2875-2896, 2012.

T. F. Massoud and A. Kalnins, Glioblastoma Invoking "Killer" Rabbits of the Middle Ages, World Neurosurg, vol.92, pp.140-141, 2016.

L. Matlock-colangelo, D. Cho, C. Pitner, M. W. Frey, and A. J. Baeumer, Functionalized electrospun nanofibers as bioseparators in microfluidic systems, Lab Chip, vol.12, pp.1696-1701, 2012.

R. Mendelsohn, P. Cheung, L. Berger, E. Partridge, K. Lau et al., , 2007.

, Complex N-glycan and metabolic control in tumor cells, Cancer Res, vol.67, pp.9771-9780

C. T. Mierke, P. Kollmannsberger, D. P. Zitterbart, G. Diez, T. M. Koch et al., Vinculin facilitates cell invasion into three-dimensional collagen matrices, J Biol Chem, vol.285, pp.13121-13130, 2010.
DOI : 10.1074/jbc.m109.087171

URL : http://www.jbc.org/content/285/17/13121.full.pdf

S. Monferran, N. Skuli, C. Delmas, G. Favre, J. Bonnet et al., , 2008.

, Alphavbeta3 and alphavbeta5 integrins control glioma cell response to ionising radiation through ILK and RhoB, Int J Cancer, vol.123, pp.357-364

K. L. Mooney, W. Choy, S. Sidhu, P. Pelargos, T. T. Bui et al., The role of CD44 in glioblastoma multiforme, J Clin Neurosci, vol.34, pp.1-5, 2016.

W. Morelle and J. C. Michalski, Analysis of protein glycosylation by mass spectrometry, Nature protocols, vol.2, pp.1585-1602, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00168244

D. Moretti, B. Bello, G. Allavena, and E. Maellaro, Calpains and cancer: friends or enemies?, Arch Biochem Biophys, vol.564, pp.26-36, 2014.
DOI : 10.1016/j.abb.2014.09.018

J. R. Moskal, R. A. Kroes, D. , and G. , The glycobiology of brain tumors: disease relevance and therapeutic potential, Expert Rev Neurother, vol.9, pp.1529-1545, 2009.

I. R. Nabi, J. Shankar, and J. W. Dennis, The galectin lattice at a glance, J Cell Sci, vol.128, pp.2213-2219, 2015.

M. Nagae, Y. , and Y. , Function and 3D structure of the N-glycans on glycoproteins, Int J Mol Sci, vol.13, pp.8398-8429, 2012.

M. Nakada, E. Nambu, N. Furuyama, Y. Yoshida, T. Takino et al., Integrin alpha3 is overexpressed in glioma stem-like cells and promotes invasion, Br J Cancer, vol.108, pp.2516-2524, 2013.

D. Naor, S. Nedvetzki, I. Golan, L. Melnik, and Y. Faitelson, CD44 in cancer, Crit Rev Clin Lab Sci, vol.39, pp.527-579, 2002.

J. Nelson, N. V. Mcferran, G. Pivato, E. Chambers, C. Doherty et al., The 67 kDa laminin receptor: structure, function and role in disease, Biosci Rep, vol.28, pp.33-48, 2008.

C. Nicholson and E. Sykova, Extracellular space structure revealed by diffusion analysis, Trends Neurosci, vol.21, pp.207-215, 1998.

C. M. Niessen, Tight junctions/adherens junctions: basic structure and function, J Invest Dermatol, vol.127, pp.2525-2532, 2007.

U. Novak and A. H. Kaye, Extracellular matrix and the brain: components and function, J Clin Neurosci, vol.7, pp.280-290, 2000.

K. Ohtsubo, M. , and J. D. , Glycosylation in cellular mechanisms of health and disease, Cell, vol.126, pp.855-867, 2006.

B. Ortensi, M. Setti, D. Osti, and G. Pelicci, Cancer stem cell contribution to glioblastoma invasiveness, Stem Cell Res Ther, vol.4, p.18, 2013.

A. A. Padhiar, J. Fan, Y. Tang, J. Yu, S. Wang et al., Upregulated beta1-6 branch N-glycan marks early gliomagenesis but exhibited biphasic expression in the progression of astrocytic glioma, Am J Cancer Res, vol.5, pp.1101-1116, 2015.

L. Pan, Y. Zhao, Z. Yuan, and G. Qin, Research advances on structure and biological functions of integrins. Springerplus 5, p.1094, 2016.

K. Pankova, D. Rosel, M. Novotny, and J. Brabek, The molecular mechanisms of transition between mesenchymal and amoeboid invasiveness in tumor cells, Cell Mol Life Sci, vol.67, pp.63-71, 2010.

J. B. Park, H. J. Kwak, and S. H. Lee, Role of hyaluronan in glioma invasion, Cell Adh Migr, vol.2, pp.202-207, 2008.

J. J. Parker, K. R. Dionne, R. Massarwa, M. Klaassen, N. K. Foreman et al., Gefitinib selectively inhibits tumor cell migration in EGFR-amplified human glioblastoma, Neuro Oncol, vol.15, pp.1048-1057, 2013.

D. W. Parsons, S. Jones, X. Zhang, J. C. Lin, R. J. Leary et al., An integrated genomic analysis of human glioblastoma multiforme, Science, vol.321, pp.1807-1812, 2008.

E. A. Partridge, C. Le-roy, G. M. Di-guglielmo, J. Pawling, P. Cheung et al., Regulation of cytokine receptors by Golgi N-glycan processing and endocytosis, Science, vol.306, pp.120-124, 2004.

L. S. Payne and P. H. Huang, The pathobiology of collagens in glioma, Mol Cancer Res, vol.11, pp.1129-1140, 2013.

F. Peglion, F. Llense, E. , and S. , Adherens junction treadmilling during collective migration, Nat Cell Biol, vol.16, pp.639-651, 2014.
DOI : 10.1038/ncb2985

G. S. Perng, M. Shoreibah, I. Margitich, M. Pierce, and N. Fregien, Expression of Nacetylglucosaminyltransferase V mRNA in mammalian tissues and cell lines, Glycobiology, vol.4, pp.867-871, 1994.

A. Pestana, J. Vinagre, M. Sobrinho-simoes, and P. Soares, TERT biology and function in cancer: beyond immortalisation, J Mol Endocrinol, vol.58, pp.129-146, 2017.

M. W. Pickup, J. K. Mouw, and V. M. Weaver, The extracellular matrix modulates the hallmarks of cancer, EMBO Rep, vol.15, pp.1243-1253, 2014.

N. Pouliot and N. Kusuma, Laminin-511: a multi-functional adhesion protein regulating cell migration, tumor invasion and metastasis, Cell Adh Migr, vol.7, pp.142-149, 2013.

V. Ramovs, L. Te-molder, and A. Sonnenberg, The opposing roles of laminin-binding integrins in cancer, Matrix Biol, vol.57, pp.213-243, 2017.

M. Ranjit, K. Motomura, F. Ohka, T. Wakabayashi, and A. Natsume, Applicable advances in the molecular pathology of glioblastoma, Brain Tumor Pathol, vol.32, pp.153-162, 2015.

J. Rao, L. , and N. , Microfilament actin remodeling as a potential target for cancer drug development, Curr Cancer Drug Targets, vol.4, pp.345-354, 2004.

J. S. Rao, Molecular mechanisms of glioma invasiveness: the role of proteases, Nat Rev Cancer, vol.3, pp.489-501, 2003.

S. S. Rao, J. J. Lannutti, M. S. Viapiano, A. Sarkar, and J. O. Winter, Toward 3D biomimetic models to understand the behavior of glioblastoma multiforme cells, Tissue Eng Part B Rev, vol.20, pp.314-327, 2014.

S. S. Rao, M. T. Nelson, R. Xue, J. K. Dejesus, M. S. Viapiano et al.,

R. R. Rayavarapu, B. Heiden, N. Pagani, M. M. Shaw, S. Shuff et al., The role of multicellular aggregation in the survival of ErbB2-positive breast cancer cells during extracellular matrix detachment, J Biol Chem, vol.290, pp.8722-8733, 2015.

M. Reffay, M. C. Parrini, O. Cochet-escartin, B. Ladoux, A. Buguin et al., , 2014.

, Med Sci, vol.30, pp.736-738

J. Relucio, M. J. Menezes, Y. Miyagoe-suzuki, S. Takeda, and H. Colognato, Laminin regulates postnatal oligodendrocyte production by promoting oligodendrocyte progenitor survival in the subventricular zone, Glia, vol.60, pp.1451-1467, 2012.

D. T. Ross, U. Scherf, M. B. Eisen, C. M. Perou, C. Rees et al., Systematic variation in gene expression patterns in human cancer cell lines, Nat Genet, vol.24, pp.227-235, 2000.

M. C. Ryczko, J. Pawling, R. Chen, A. M. Rahman, K. Yau et al., Metabolic Reprogramming by, Hexosamine Biosynthetic and Golgi N-Glycan Branching Pathways. Sci Rep, vol.6, p.23043, 2016.

J. Sabatte, W. Faigle, A. Ceballos, W. Morelle, C. Rodriguez-rodrigues et al., Semen clusterin is a novel DC-SIGN ligand, J Immunol, vol.187, pp.5299-5309, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00871196

H. Schachter, Biosynthetic controls that determine the branching and microheterogeneity of proteinbound oligosaccharides, Biochem Cell Biol, vol.64, pp.163-181, 1986.

J. Schittenhelm, G. Tabatabai, and B. Sipos, The role of integrins in primary and secondary brain tumors, Histol Histopathol, vol.31, pp.1069-1078, 2016.

O. Schnell, B. Krebs, E. Wagner, A. Romagna, A. J. Beer et al., Expression of integrin alphavbeta3 in gliomas correlates with tumor grade and is not restricted to tumor vasculature, Brain Pathol, vol.18, pp.378-386, 2008.

S. Sell, Stem cell origin of cancer and differentiation therapy, Crit Rev Oncol Hematol, vol.51, pp.1-28, 2004.

S. Sen, W. P. Ng, and S. Kumar, Contributions of talin-1 to glioma cell-matrix tensional homeostasis, J R Soc Interface, vol.9, pp.1311-1317, 2012.

V. Senner, S. Ratzinger, S. Mertsch, S. Grassel, and W. Paulus, Collagen XVI expression is upregulated in glioblastomas and promotes tumor cell adhesion, FEBS Lett, vol.582, pp.3293-3300, 2008.

B. Serrels, A. Serrels, V. G. Brunton, M. Holt, G. W. Mclean et al., Focal adhesion kinase controls actin assembly via a FERM-mediated interaction with the Arp2/3 complex, Nat Cell Biol, vol.9, pp.1046-1056, 2007.

E. Serres, F. Debarbieux, F. Stanchi, L. Maggiorella, D. Grall et al., Fibronectin expression in glioblastomas promotes cell cohesion, collective invasion of basement membrane in vitro and orthotopic tumor growth in mice, Oncogene, vol.33, pp.3451-3462, 2014.
URL : https://hal.archives-ouvertes.fr/hal-00862133

N. Shologu, E. Szegezdi, A. Lowery, M. Kerin, A. Pandit et al., Recreating complex pathophysiologies in vitro with extracellular matrix surrogates for anticancer therapeutics screening, Drug Discov Today, vol.21, pp.1521-1531, 2016.

M. Shoreibah, G. S. Perng, B. Adler, J. Weinstein, R. Basu et al., Isolation, characterization, and expression of a cDNA encoding Nacetylglucosaminyltransferase V, J Biol Chem, vol.268, pp.15381-15385, 1993.

F. A. Siebzehnrubl, B. A. Reynolds, A. Vescovi, D. A. Steindler, and L. P. Deleyrolle, The origins of glioma: E Pluribus Unum, vol.59, pp.1135-1147, 2011.

M. Silginer, M. Weller, U. Ziegler, R. , and P. , Integrin inhibition promotes atypical anoikis in glioma cells, Cell Death Dis, vol.5, p.1012, 2014.

G. A. Silva, C. Czeisler, K. L. Niece, E. Beniash, D. A. Harrington et al., Selective differentiation of neural progenitor cells by high-epitope density nanofibers, Science, vol.303, pp.1352-1355, 2004.

D. J. Silver, F. A. Siebzehnrubl, M. J. Schildts, A. T. Yachnis, G. M. Smith et al., Chondroitin sulfate proteoglycans potently inhibit invasion and serve as a central organizer of the brain tumor microenvironment, J Neurosci, vol.33, pp.15603-15617, 2013.

D. J. Silver and J. Silver, Contributions of chondroitin sulfate proteoglycans to neurodevelopment, injury, and cancer, Curr Opin Neurobiol, vol.27, pp.171-178, 2014.

S. K. Singh, I. D. Clarke, M. Terasaki, V. E. Bonn, C. Hawkins et al., Identification of a cancer stem cell in human brain tumors, Cancer Res, vol.63, pp.5821-5828, 2003.

S. T. Sit and E. Manser, Rho GTPases and their role in organizing the actin cytoskeleton, J Cell Sci, vol.124, pp.679-683, 2011.

K. E. Sloan, J. K. Stewart, A. F. Treloar, R. T. Matthews, J. et al., CD155/PVR enhances glioma cell dispersal by regulating adhesion signaling and focal adhesion dynamics, Cancer Res, vol.65, pp.10930-10937, 2005.

M. J. Son, K. Woolard, D. H. Nam, J. Lee, and H. A. Fine, SSEA-1 is an enrichment marker for tumorinitiating cells in human glioblastoma, Cell Stem Cell, vol.4, pp.440-452, 2009.

I. C. Sroka, T. A. Anderson, K. M. Mcdaniel, R. B. Nagle, M. B. Gretzer et al., The laminin binding integrin alpha6beta1 in prostate cancer perineural invasion, J Cell Physiol, vol.224, pp.283-288, 2010.

S. J. Storr, S. Zhang, T. Perren, M. Lansdown, H. Fatayer et al., The calpain system is associated with survival of breast cancer patients with large but operable inflammatory and non-inflammatory tumours treated with neoadjuvant chemotherapy, Oncotarget, vol.7, pp.47927-47937, 2016.

R. Stupp, W. P. Mason, M. J. Van-den-bent, M. Weller, B. Fisher et al., Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma, N Engl J Med, vol.352, pp.987-996, 2005.

A. Subramanian, A. Harris, K. Piggott, C. Shieff, and R. Bradford, Metastasis to and from the central nervous system--the 'relatively protected site, Lancet Oncol, vol.3, pp.498-507, 2002.

K. Tabu, A. Ohnishi, Y. Sunden, T. Suzuki, M. Tsuda et al., , 2006.

, A novel function of OLIG2 to suppress human glial tumor cell growth via p27Kip1 transactivation, J Cell Sci, vol.119, pp.1433-1441

C. P. Tanase, A. M. Enciu, S. Mihai, A. I. Neagu, B. Calenic et al., Anti-cancer Therapies in High Grade Gliomas, Curr Proteomics, vol.10, pp.246-260, 2013.
DOI : 10.2174/1570164611310030007

URL : http://europepmc.org/articles/pmc3821381?pdf=render

K. Tanner and M. M. Gottesman, Beyond 3D culture models of cancer, Sci Transl Med, vol.7, pp.283-289, 2015.
DOI : 10.1126/scitranslmed.3009367

URL : http://europepmc.org/articles/pmc5063633?pdf=render

U. Theisen, E. Straube, and A. Straube, Directional persistence of migrating cells requires Kif1C-mediated stabilization of trailing adhesions, Dev Cell, vol.23, pp.1153-1166, 2012.

A. D. Theocharis, S. S. Skandalis, C. Gialeli, and N. K. Karamanos, Extracellular matrix structure, Adv Drug Deliv Rev, vol.97, pp.4-27, 2016.

A. Thomas, M. Tanaka, J. Trepel, W. C. Reinhold, V. N. Rajapakse et al., Temozolomide in the Era of Precision Medicine, Cancer Res, vol.77, pp.823-826, 2017.

R. G. Thorne and C. Nicholson, In vivo diffusion analysis with quantum dots and dextrans predicts the width of brain extracellular space, Proc Natl Acad Sci U S A, vol.103, pp.5567-5572, 2006.

B. Todd, D. Moore, C. C. Deivanayagam, G. D. Lin, D. Chattopadhyay et al., A structural model for the inhibition of calpain by calpastatin: crystal structures of the native domain VI of calpain and its complexes with calpastatin peptide and a small molecule inhibitor, J Mol Biol, vol.328, pp.131-146, 2003.

A. L. Trepant, C. Bouchart, S. Rorive, S. Sauvage, C. Decaestecker et al., Identification of OLIG2 as the most specific glioblastoma stem cell marker starting from comparative analysis of data from similar DNA chip microarray platforms, Tumour Biol, vol.36, pp.1943-1953, 2015.

C. Tucker-burden, P. Chappa, M. Krishnamoorthy, B. A. Gerwe, C. D. Scharer et al., Lectins identify glycan biomarkers on glioblastoma-derived cancer stem cells, Stem Cells Dev, vol.21, pp.2374-2386, 2012.
DOI : 10.1089/scd.2011.0369

URL : http://europepmc.org/articles/pmc3425159?pdf=render

S. G. Turner, T. Gergel, H. Wu, M. Lacroix, and S. A. Toms, The effect of field strength on glioblastoma multiforme response in patients treated with the NovoTTF-100A system, World J Surg Oncol, vol.12, p.162, 2014.

B. B. Tysnes, L. F. Larsen, G. O. Ness, R. Mahesparan, K. Edvardsen et al., Stimulation of glioma-cell migration by laminin and inhibition by anti-alpha3 and anti-beta1 integrin antibodies, Int J Cancer, vol.67, pp.777-784, 1996.

N. Uchida, D. W. Buck, D. He, M. J. Reitsma, M. Masek et al., Direct isolation of human central nervous system stem cells, Proc Natl Acad Sci U S A, vol.97, pp.14720-14725, 2000.

T. A. Ulrich, E. M. De-juan-pardo, and S. Kumar, The mechanical rigidity of the extracellular matrix regulates the structure, motility, and proliferation of glioma cells, Cancer Res, vol.69, pp.4167-4174, 2009.

V. Umesh, A. D. Rape, T. A. Ulrich, and S. Kumar, Microenvironmental stiffness enhances glioma cell proliferation by stimulating epidermal growth factor receptor signaling, PLoS One, vol.9, 2014.
DOI : 10.1371/journal.pone.0101771

URL : https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0101771&type=printable

K. Urbanska, J. Sokolowska, M. Szmidt, and P. Sysa, Glioblastoma multiforme -an overview, Contemp Oncol (Pozn), vol.18, pp.307-312, 2014.

E. G. Van-meir, C. G. Hadjipanayis, A. D. Norden, H. K. Shu, P. Y. Wen et al., Exciting new advances in neuro-oncology: the avenue to a cure for malignant glioma, CA Cancer J Clin, vol.60, pp.166-193, 2010.

A. Vasconcelos-dos-santos, I. A. Oliveira, M. C. Lucena, N. R. Mantuano, S. A. Whelan et al., Biosynthetic Machinery Involved in Aberrant Glycosylation: Promising Targets for Developing of, Drugs Against Cancer. Front Oncol, vol.5, p.138, 2015.

R. G. Verhaak, K. A. Hoadley, E. Purdom, V. Wang, Y. Qi et al., Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1, Cancer Cell, vol.17, pp.98-110, 2010.

M. Vicente-manzanares, D. J. Webb, and A. R. Horwitz, Cell migration at a glance, J Cell Sci, vol.118, pp.4917-4919, 2005.

C. Wang, X. Tong, Y. , and F. , Bioengineered 3D brain tumor model to elucidate the effects of matrix stiffness on glioblastoma cell behavior using PEG-based hydrogels, Mol Pharm, vol.11, pp.2115-2125, 2014.

A. Weeks, N. Okolowsky, B. Golbourn, S. Ivanchuk, C. Smith et al., ECT2 and RASAL2 mediate mesenchymal-amoeboid transition in human astrocytoma cells, Am J Pathol, vol.181, pp.662-674, 2012.

R. A. Weinberg, he Biology of Cancer, 2013.

K. E. Wellen, C. Lu, A. Mancuso, J. M. Lemons, M. Ryczko et al., The hexosamine biosynthetic pathway couples growth factor-induced glutamine uptake to glucose metabolism, Genes Dev, vol.24, pp.2784-2799, 2010.

T. A. Wilson, M. A. Karajannis, and D. H. Harter, Glioblastoma multiforme: State of the art and future therapeutics, Surg Neurol Int, vol.5, p.64, 2014.

S. E. Winograd-katz, R. Fassler, B. Geiger, and K. R. Legate, The integrin adhesome: from genes and proteins to human disease, Nat Rev Mol Cell Biol, vol.15, pp.273-288, 2014.

S. Y. Wong and S. Kumar, Matrix regulation of tumor-initiating cells, Prog Mol Biol Transl Sci, vol.126, pp.243-256, 2014.

Y. Wu, J. Wang, Y. Shi, H. Pu, R. K. Leak et al., Implantation of Brain-derived Extracellular Matrix Enhances Neurological Recovery after Traumatic Brain Injury, Cell Transplant, 2016.

N. Yamaguchi, T. Mizutani, K. Kawabata, and H. Haga, Leader cells regulate collective cell migration via Rac activation in the downstream signaling of integrin beta1 and PI3K, Sci Rep, vol.5, p.7656, 2015.

H. Yamamoto, J. Swoger, S. Greene, T. Saito, J. Hurh et al., Beta1,6-N-acetylglucosamine-bearing N-glycans in human gliomas: implications for a role in regulating invasivity, vol.60, pp.134-142, 2000.

Y. L. Yang, S. Motte, and L. J. Kaufman, Pore size variable type I collagen gels and their interaction with glioma cells, Biomaterials, vol.31, pp.5678-5688, 2010.

M. Yao, B. T. Goult, B. Klapholz, X. Hu, C. P. Toseland et al., The mechanical response of talin, Nat Commun, vol.7, p.11966, 2016.

X. Ye, M. A. Mclean, and S. G. Sligar, Conformational equilibrium of talin is regulated by anionic lipids, Biochim Biophys Acta, vol.1858, pp.1833-1840, 2016.

Y. N. Yordanova and H. Duffau, Supratotal resection of diffuse gliomas -an overview of its multifaceted implications, Neurochirurgie, 2017.

T. Yoshimura, Y. Kawano, N. Arimura, S. Kawabata, A. Kikuchi et al., GSK-3beta regulates phosphorylation of CRMP-2 and neuronal polarity, Cell, vol.120, pp.137-149, 2005.

R. Zent and A. Pozzi, Cell-Extracellular Matrix Interactions in Cancer, 1 edn, 2010.

X. Zhao and J. L. Guan, Focal adhesion kinase and its signaling pathways in cell migration and angiogenesis, Adv Drug Deliv Rev, vol.63, pp.610-615, 2011.

J. Zhong, J. B. Baquiran, N. Bonakdar, J. Lees, Y. W. Ching et al., NEDD9 stabilizes focal adhesions, increases binding to the extra-cellular matrix and differentially effects 2D versus 3D cell migration, PLoS One, vol.7, p.35058, 2012.