Transmembrane protein 18 enhances the tropism of neural stem cells for glioma cells

被引:68
作者
Jurvansuu, Jaana [1 ]
Zhao, Ying [1 ,4 ]
Leung, Doreen S. Y. [1 ]
Boulaire, Jerome [1 ]
Yu, Yuan Hong [2 ,3 ]
Ahmed, Sohail [2 ,3 ]
Wang, Shu [1 ,4 ]
机构
[1] Inst Bioengn & Nanotechnol, Singapore 138669, Singapore
[2] Inst Med Biol, Singapore, Singapore
[3] Natl Univ Singapore, Dept Physiol, Singapore 117548, Singapore
[4] Natl Univ Singapore, Dept Biol Sci, Singapore 117548, Singapore
关键词
D O I
10.1158/0008-5472.CAN-07-5291
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The failure of current glioma therapies is mainly due to the ability of the tumor cells to invade extensively the surrounding healthy brain tissue, hence escaping localized treatments. Neural stem cells (NSC) are able to home in on tumor foci at sites distant from the main tumor mass, possibly enabling treatment of scattered glioma clusters. To make the strategy more effective, we performed a cDNA expression library screening to identify the candidate genes that once overexpressed would enhance the tropism of NSCs for gliomas. Here, we show that a previously unannotated gene, the one encoding transmembrane protein 18 (TMEM18), is one such gene. Overexpression of TMEM18 was seen in the current study to provide NSCs and neural precursors an increased migration capacity toward glioblastoma cells in vitro and in the rat brain. Functional inactivation of the TMEM18 gene resulted in almost complete loss of the migration activity of these cells. Thus, TMEM18 is a novel cell migration modulator. Overexpression of this protein could be favorably used in NSC-based glioma therapy.
引用
收藏
页码:4614 / 4622
页数:9
相关论文
共 28 条
[1]   Migration and differentiation of neural precursor cells can be directed by microglia [J].
Aarum, J ;
Sandberg, K ;
Haeberlein, SLB ;
Persson, MAA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (26) :15983-15988
[2]   Neural stem cells display extensive tropism for pathology in adult brain: Evidence from intracranial gliomas [J].
Aboody, KS ;
Brown, A ;
Rainov, NG ;
Bower, KA ;
Liu, SX ;
Yang, W ;
Small, JE ;
Herrlinger, U ;
Ourednik, V ;
Black, PM ;
Breakefield, XO ;
Snyder, EY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12846-12851
[3]   Murine neuronal progenitor cells are preferentially recruited to tumor vasculature via α4-integrin and SDF-1α-dependent mechanisms [J].
Allport, JR ;
Patil, VRS ;
Weissleder, R .
CANCER BIOLOGY & THERAPY, 2004, 3 (09) :838-844
[4]  
[Anonymous], 1993, Biol. Chem. Hoppe Seyler, DOI DOI 10.1515/BCHM3.1993.374.1-6.143
[5]   Neural precursor cells as carriers for a gene therapeutical approach in tumor therapy [J].
Arnhold, S ;
Hilgers, M ;
Lenartz, D ;
Semkova, I ;
Kochanek, S ;
Voges, J ;
Andressen, C ;
Addicks, K .
CELL TRANSPLANTATION, 2003, 12 (08) :827-837
[6]   Gene therapy of experimental brain tumors using neural progenitor cells [J].
Benedetti, S ;
Pirola, B ;
Pollo, B ;
Magrassi, L ;
Bruzzone, MG ;
Rigamonti, D ;
Galli, R ;
Selleri, S ;
Di Meco, F ;
De Fraja, C ;
Vescovi, A ;
Cattaneo, E ;
Finocchiaro, G .
NATURE MEDICINE, 2000, 6 (04) :447-450
[7]   Constitutive EGFR signaling confers a motile phenotype to neural stem cells [J].
Boockvar, JA ;
Kapitonov, D ;
Kapoor, G ;
Schouten, J ;
Counelis, GJ ;
Bogler, O ;
Snyder, EY ;
McIntosh, TK ;
O'Rourke, DM .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 24 (04) :1116-1130
[8]   Intravascular delivery of neural stem cell lines to target intracranial and extracranial tumors of neural and non-neural origin [J].
Brown, AB ;
Yang, W ;
Schmidt, NO ;
Carroll, R ;
Leishear, KK ;
Rainov, NG ;
Black, PM ;
Breakefield, XO ;
Aboody, KS .
HUMAN GENE THERAPY, 2003, 14 (18) :1777-1785
[9]   CXCR4 expression mediates glioma cell invasiveness [J].
Ehtesham, M ;
Winston, JA ;
Kabos, P ;
Thompson, RC .
ONCOGENE, 2006, 25 (19) :2801-2806
[10]   Glioma tropic neural stem cells consist of astrocytic precursors and their migratory capacity is mediated by CXCR4 [J].
Ehtesham, M ;
Yuan, XP ;
Kabos, P ;
Chung, NHC ;
Liu, GT ;
Akasaki, Y ;
Black, KL ;
Yu, JS .
NEOPLASIA, 2004, 6 (03) :287-293