Literature DB >> 14628206

Soluble factors involved in glioma invasion.

M M Mueller1, T Werbowetski, R F Del Maestro.   

Abstract

Recent studies using molecular and cellular techniques of the factors regulating the invasion process have revealed a crucial role for a number of growth factors and cytokines. Their function lies on the one hand in the autocrine stimulation of the tumor cells themselves, resulting in the stimulation of protease expression and an enhancement of migratory potential. On the other hand, the growth factors and cytokines seem to play a major role in the paracrine activation of the tumor surrounding stroma. Through stimulation of the strong angiogenic response that is characteristic for gliomas and also of the expression of proteases in the stromal cells, they contribute critically to the generation of a stromal environment that is permissive or even inductive for tumor cell invasion. Understanding of the mechanisms by which soluble factors modulate glioma cell invasion therefore will help to determine targets for the modification of existing therapies and lead to the development of novel therapeutic strategies in the management of gliomas.

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Year:  2003        PMID: 14628206     DOI: 10.1007/s00701-003-0132-0

Source DB:  PubMed          Journal:  Acta Neurochir (Wien)        ISSN: 0001-6268            Impact factor:   2.216


  11 in total

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Authors:  Ingo Fricke; Dmitry I Gabrilovich
Journal:  Immunol Invest       Date:  2006       Impact factor: 3.657

2.  HGF upregulates CXCR4 expression in gliomas via NF-kappaB: implications for glioma cell migration.

Authors:  Mine Esencay; Elizabeth W Newcomb; David Zagzag
Journal:  J Neurooncol       Date:  2010-02-16       Impact factor: 4.130

3.  Low Concentration Microenvironments Enhance the Migration of Neonatal Cells of Glial Lineage.

Authors:  Richard A Able; Celestin Ngnabeuye; Cade Beck; Eric C Holland; Maribel Vazquez
Journal:  Cell Mol Bioeng       Date:  2012-06       Impact factor: 2.321

4.  Sphingosine-1-phosphate and interleukin-1 independently regulate plasminogen activator inhibitor-1 and urokinase-type plasminogen activator receptor expression in glioblastoma cells: implications for invasiveness.

Authors:  Lauren Bryan; Barbara S Paugh; Dmitri Kapitonov; Katarzyna M Wilczynska; Silvina M Alvarez; Sandeep K Singh; Sheldon Milstien; Sarah Spiegel; Tomasz Kordula
Journal:  Mol Cancer Res       Date:  2008-09       Impact factor: 5.852

5.  EGF regulates plasminogen activator inhibitor-1 (PAI-1) by a pathway involving c-Src, PKCdelta, and sphingosine kinase 1 in glioblastoma cells.

Authors:  Barbara S Paugh; Steven W Paugh; Lauren Bryan; Dmitri Kapitonov; Katarzyna M Wilczynska; Sunita M Gopalan; Hanna Rokita; Sheldon Milstien; Sarah Spiegel; Tomasz Kordula
Journal:  FASEB J       Date:  2007-09-12       Impact factor: 5.191

6.  Interleukin-1β and transforming growth factor-β cooperate to induce neurosphere formation and increase tumorigenicity of adherent LN-229 glioma cells.

Authors:  Lei Wang; Ziyan Liu; Sivasai Balivada; Tej Shrestha; Stefan Bossmann; Marla Pyle; Loretta Pappan; Jishu Shi; Deryl Troyer
Journal:  Stem Cell Res Ther       Date:  2012-02-10       Impact factor: 6.832

7.  Polarized regulation of glycogen synthase kinase-3β is important for glioma cell invasion.

Authors:  Qifei Zou; Ying Hou; Feng Shen; Yizheng Wang
Journal:  PLoS One       Date:  2013-12-03       Impact factor: 3.240

Review 8.  Impact of the prolymphangiogenic crosstalk in the tumor microenvironment on lymphatic cancer metastasis.

Authors:  Simona L Schlereth; Nasrin Refaian; Sandra Iden; Claus Cursiefen; Ludwig M Heindl
Journal:  Biomed Res Int       Date:  2014-09-01       Impact factor: 3.411

Review 9.  The inflammatory network: bridging senescent stroma and epithelial tumorigenesis.

Authors:  Weiwei Shan; Gong Yang; Jinsong Liu
Journal:  Front Biosci (Landmark Ed)       Date:  2009-01-01

10.  IL-32θ inhibits stemness and epithelial-mesenchymal transition of cancer stem cells via the STAT3 pathway in colon cancer.

Authors:  Yesol Bak; Taeho Kwon; In Seon Bak; Jintae Hong; Dae-Yeul Yu; Do-Young Yoon
Journal:  Oncotarget       Date:  2016-02-09
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