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
[21]   Selective migration of neuralized embryonic stem cells to stem cell factor and media conditioned by glioma cell lines [J].
Serfozo, Peter ;
Schlarman, Maggie S. ;
Pierret, Chris ;
Maria, Bernard L. ;
Kirk, Mark D. .
CANCER CELL INTERNATIONAL, 2006, 6 (1)
[22]   Neuronally expressed stem cell factor induces neural stem cell migration to areas of brain injury [J].
Sun, LX ;
Lee, JW ;
Fine, HA .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (09) :1364-1374
[23]   Chemokine receptors: Signposts to brain development and disease [J].
Tran, PB ;
Miller, RJ .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (06) :444-455
[24]  
Tysnes BB, 2001, J NEURO-ONCOL, V53, P129
[25]   Human lymphoblastoid cells produce extracellular matrix degrading enzymes and induce endothelial cell proliferation, migration, morphogenesis, and angiogenesis [J].
Vacca, A ;
Ribatti, D ;
Iurlaro, M ;
Albini, A ;
Minischetti, M ;
Bussolino, F ;
Pellegrino, A ;
Ria, R ;
Rusnati, M ;
Presta, M ;
Vincenti, V ;
Persico, MG ;
Dammacco, F .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1998, 28 (01) :55-68
[26]   MCP-1 induces migration of adult neural stem cells [J].
Widera, D ;
Holtkamp, W ;
Entschladen, F ;
Niggemann, B ;
Zänker, K ;
Kaltschmidt, B ;
Kaltschmidt, C .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2004, 83 (08) :381-387
[27]   Baculoviral vector-mediated transient and stable transgene expression in human embryonic stem cells [J].
Zeng, Jieming ;
Du, Juan ;
Zhao, Ying ;
Palanisamy, Nallasivam ;
Wang, Shu .
STEM CELLS, 2007, 25 (04) :1055-1061
[28]   Glioma-produced extracellular matrix influences brain tumor tropism of human neural stem cells [J].
Ziu, Mateo ;
Schmidt, Nils Ole ;
Cargioli, Theresa G. ;
Aboody, Karen S. ;
Black, Peter McL. ;
Carroll, Rona S. .
JOURNAL OF NEURO-ONCOLOGY, 2006, 79 (02) :125-133