References
- Klekner A, Virga J, Toth J, Hortobagyi T, Der A, Szemcsak C, et al. The role of extracellular matrix components in the invasion of intracranial malignancies. Magy Onkol. Hungary. 2013;57(4):222–231.
- Claes A, Idema AJ, Wesseling P. Diffuse glioma growth: a guerilla war. Acta Neuropathol.. 2007;114(5):443–458.
- LemCrossed D, Signe JM, Clavreul A, Menei P. Intratumoral heterogeneity in glioblastoma: don’t forget the peritumoral brain zone. Neuro Oncol. 2015;17(10):1322–1332.
- Ostrom QT, Gittleman H, Liao P, Rouse C, Chen Y, Dowling J, et al. CBTRUS Statistical Report: primary brain and central nervous system tumors diagnosed in the United States in 2007–2011. Neuro-Oncology [Internet]. 2014;16(4):iv1–iv63. Available from: http://neuro-oncology.oxfordjournals.org/content/16/suppl_4/iv1.short
- Goodenberger ML, Jenkins RB. Genetics of adult glioma. Cancer Genet [Internet]. 2012;205(12):613–621. Available from: http://www.sciencedirect.com/science/article/pii/S2210776212002608
- Louis DN, Perry A, Reifenberger G, von Deimling A, Figarella-Branger D, Cavenee WK, et al. The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol [Internet]. 2016;131(6):803–820. Available from: http://link.springer.com/10.1007/s00401-016-1545-1
- Pouratian N, Schiff D. Management of low-grade glioma. Curr Neurol Neurosci Rep. 2010;10(3):224–231.
- Markert JM. The role of early resection vs Biopsy in the management of low-grade gliomasearly vs late surgery in low-grade gliomas. JAMA [Internet]. 2012;308(18):1918–1919. Available from: http://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=23099540&retmode=ref&cmd=prlinks%5Cnpapers3://publication/doi/10.1001/jama.2012.14523
- van den Bent MJ, Snijders TJ, Bromberg JEC. Current treatment of low grade gliomas. Memo. 2012;5(3):223–227. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3458190&tool=pmcentrez&rendertype=abstract
- Pedersen CL, Romner B. Current treatment of low grade astrocytoma: a review. Clin Neurol and Neurosurg Netherlands. 2013;115(1):1–8.
- Lind-Landström T, Habberstad AH, Sundstrøm S, Torp SH. Prognostic value of histological features in diffuse astrocytomas WHO grade II. Int J Clin Exp Pathol. 2012;5(2):152–158.
- Klekner A, Varga I, Bognár L, Hutóczki G, Kenyeres A, Tóth J, et al. Extracellular matrix of cerebral tumors with different invasiveness. Ideggyogy Sz. 2010;63(1–2):38–43.
- Bouterfa H, Darlapp AR, Klein E, Pietsch T, Roosen K, Tonn JC. Expression of different extracellular matrix components in human brain tumor and melanoma cells in respect to variant culture conditions. J Neurooncol [Internet]. 1999;44(1):23–33. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10582665
- Chintala SK, Rao JK. Invasion of human glioma: role of extracellular matrix proteins. Front Biosci. 1996;1:d324–d339.
- Petrás M, Hutóczki G, Varga I, Vereb G, Szöllősi J, Bognár L, et al. Expression pattern of invasion-related molecules in cerebral tumors of different origin. Magyar Onkológia. 2009;53(3):253–258.
- Zamecnik J, Vargova L, Homola A, Kodet R, Sykova E. Extracellular matrix glycoproteins and diffusion barriers in human astrocytic tumours. Neuropathol Appl Neurobiol. 2004;30(4):338–350.
- Varga I, Hutóczki G, Szemcsák CD, Zahuczky G, Tóth J, Adamecz Z, et al. Brevican, neurocan, tenascin-C and versican are mainly responsible for the invasiveness of low-grade astrocytoma. Pathol Oncol Res. 2012;18(2):413–420.
- Klekner Á, Hutóczki G, Virga J, Reményi-Puskár J, Tóth J, Scholtz B, et al. Expression pattern of invasion-related molecules in the peritumoral brain. Clin Neurol Neurosurg. 2015;139:138–143.
- Yoshida T, Matsuda Y, Naito Z, Ishiwata T. CD44 in human glioma correlates with histopathological grade and cell migration. Pathol Int. 2012;62(7):463–470.
- Pollo B. Pathological classification of brain tumors. Quart J Nuc Med Mol Imag. 2012;56:103–111.
- Johnson JD, Young B. Demographics of brain metastasis. Neurosurg Clin N Am [Internet]. 1996;7(3):337–344. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8823767
- Fox BD, Cheung VJ, Patel AJ, Suki D, Rao G. Epidemiology of metastatic brain tumors. Neurosurg Clin N Am.. 2011;22(1):1–6. Vol.
- Fisher JL, Schwartzbaum JA, Wrensch M, Wiemels JL. Epidemiology of brain tumors [Review]. Neurol Clin. 2007;25(4):867.
- Varga I, Hutóczki G, Petrás M, Scholtz B, Mikó E, Kenyeres A, et al. Expression of invasion-related extracellular matrix molecules in human glioblastoma versus intracerebral lung adenocarcinoma metastasis. Cen Eur Neurosurg. 2010;71(04):173–180. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20397122
- Takeichi M. Cadherins in cancer: implications for invasion and metastasis. Curr Opin Cell Biol [Internet]. 1993;5(5):806–811. Available from: http://www.sciencedirect.com/science/article/pii/095506749390029P
- Patarroyo M, Tryggvason K, Virtanen I. Laminin isoforms in tumor invasion, angiogenesis and metastasis. Semin Cancer Biol [Internet]. 2002;12(3):197–207. Available from: http://www.sciencedirect.com/science/article/pii/S1044579X02000238
- Wegrowski Y, Maquart F-X. Chondroitin sulfate proteoglycans in tumor progression. Adv Pharmacol [Internet]. 2006;53:297–321. Available from: http://www.sciencedirect.com/science/article/pii/S105435890553014X
- Kurtkaya-Yapicier ? ?, Scheithauer B, Woodruff JM. The pathobiologic spectrum of Schwannomas. Histology and Histopathology. 2003;18:925–934.
- Fong B, Barkhoudarian G, Pezeshkian P, Parsa AT, Gopen Q, Yang I. The molecular biology and novel treatments of vestibular schwannomas. J Neurosurg [Internet]. 2011;115(5):906–914. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21800959
- Stangerup S-E, Caye-Thomasen P. Epidemiology and natural history of vestibular schwannomas. Otolaryngol Clin North Am [Internet]. 2012;45(2):257–268. Available from: http://dx.doi.org/10.1016/j.otc.2011.12.008
- Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods. 2001;25(4):402–408.
- Bradford M. Rapid and sensitive method for quantification of microgram quantities of protein utilizing principle of protein-dye-binding. Anal Biochem. 1976;72(1–2):248–254.
- Lange V, Picotti P, Domon B, Aebersold R. Selected reaction monitoring for quantitative proteomics: a tutorial. Mol Syst Biol. 2008;4:222.
- James A, Jorgensen C. Basic design of MRM assays for peptide quantification. Methods Mol Biol. 2010;658:167–185.
- Iuga C, Seicean A, Iancu C, Buiga R, Sappa PK, Völker U, et al. Proteomic identification of potential prognostic biomarkers in resectable pancreatic ductal adenocarcinoma. Proteomics. Wiley Proteomics.. 2014;14(7–8):945–955.
- Qian W-J, Jacobs JM, Liu T, Camp DG, Smith RD. Advances and challenges in liquid chromatography-mass spectrometry-based proteomics profiling for clinical applications. Mol Cell Proteomics. 2006;5(10):1727–1744.
- Wei K-C, Huang C-Y, Chen P-Y, Feng L-Y, Wu T-WE, Chen S-M, et al. Evaluation of the prognostic value of CD44 in glioblastoma multiforme. Anticancer Res. 2010;30(1):253–259.
- Ranuncolo SM, Ladeda V, Specterman S, Varela M, Lastiri J, Morandi A, et al. CD44 expression in human gliomas. J Surg Oncol. 2002;79(1):30–35.
- Delpech B, Maingonnat C, Girard N, Chauzy C, Olivier A, Maunoury R, et al. Hyaluronan and hyaluronectin in the extracellular matrix of human brain tumour stroma. Eur J Cancer. 1993;29(7):1012–1017.
- Novak U, Stylli SS, Kaye AH, Lepperdinger G. Hyaluronidase-2 overexpression accelerates intracerebral but not subcutaneous tumor formation of murine astrocytoma cells. Cancer Res. 1999;59(24):6246–6250.
- Zoltan-Jones A, Huang L, Ghatak S, Toole BP. Elevated hyaluronan production induces mesenchymal and transformed properties in epithelial cells. J Biol Chem. 2003;278(46):45801–45810.
- Park JB, Kwak HJ, Lee SH. Role of hyaluronan in glioma invasion. Cell Adh Migr. 2008;2(3):202–207. Vol.
- Färber K, Synowitz M, Zahn G, Vossmeyer D, Stragies R, van Rooijen N, Kettenmann H. An alpha5beta1 integrin inhibitor attenuates glioma growth. Mol Cell Neurosci [Internet]. 2008;39(4):579–585. Available from: http://www.sciencedirect.com/science/article/pii/S1044743108002212
- D’Abaco GM, Kaye AH. Integrins: molecular determinants of glioma invasion. J Clin Neurosci [Internet]. 2007;14(11):1041–1048. Available from: http://www.sciencedirect.com/science/article/pii/S0967586807003797
- Tysnes BB, Larsen LF, Ness GO, Mahesparan R, Edvardsen K, Garcia-Cabrera I, Bjerkvig R. Stimulation of glioma-cell migration by laminin and inhibition by anti-alpha3 and anti-beta1 integrin antibodies. Int. J. Cancer. 1996;67(6):777–784. Available from: http://www.scopus.com/inward/record.url?eid=2-s2.0-0029981104&partnerID=tZOtx3y1
- Massagué J. TGFb in cancer. Cell [Internet]. 2008;134(2):215–230. Available from: http://dx.doi.org/10.1016/j.cell.2008.07.001
- Dong Z-Z, Yao D-F, Yao M, Qiu L-W, Zong L, Wu W, et al. Clinical impact of plasma TGF-beta1 and circulating TGF-beta1 mRNA in diagnosis of hepatocellular carcinoma. Hepatobiliary Pancreat Dis Int [Internet]. 2008;7(3):288–295. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18522884
- Xie L, Law BK, Chytil AM, Brown K. A, Aakre ME, Moses HL. Activation of the Erk pathway is required for TGF-beta1-induced EMT in vitro. Neoplasia [Internet]. 2004;6(5):603–610. Available from: http://dx.doi.org/10.1593/neo.04241
- Xu J, Lamouille S, Derynck R. TGF-beta-induced epithelial to mesenchymal transition. Cell Res. 2009;19(2):156–172. Available from: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=19153598
- Knepper JL, James AC, Ming JE. TGIF, a gene associated with human brain defects, regulates neuronal development. Dev Dyn. 2006;235(6):1482–1490.
- Zhang M-Z, Ferrigno O, Wang Z, Ohnishi M, Prunier C, Levy L, et al. TGIF governs a feed-forward network that empowers wnt signaling to drive mammary tumorigenesis. Cancer Cell. 2015;27(4):547–560.