中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Essential Role of TRPC6 Channels in G2/M Phase Transition and Development of Human Glioma

文献类型:期刊论文

作者Wang, Yizheng; Yao, Hailan
刊名JOURNAL OF THE NATIONAL CANCER INSTITUTE
出版日期2010
卷号102期号:14页码:1052-1068
关键词RECEPTOR POTENTIAL CHANNELS HUMAN-MALIGNANT GLIOMAS CELL-CYCLE PROGRESSION OPERATED CALCIUM-ENTRY DNA-DAMAGE CHECKPOINTS CENTRAL-NERVOUS-SYSTEM BREAST-CANCER CELLS GROWTH-FACTOR PDGF PROTEIN-KINASE-C IN-VIVO
ISSN号0027-8874
通讯作者Wang, YZ (reprint author), Chinese Acad Sci, Lab Neural Signal Transduct, Shanghai Inst Biol Sci, Inst Neurosci,State Key Lab Neurosci, 320 Yueyang Rd, Shanghai 200031, Peoples R China,yzwang@ion.ac.cn
英文摘要Patients with glioblastoma multiforme, the most aggressive form of glioma, have a median survival of approximately 12 months. Calcium (Ca(2+)) signaling plays an important role in cell proliferation, and some members of the Ca(2+)-permeable transient receptor potential canonical (TRPC) family of channel proteins have demonstrated a role in the proliferation of many types of cancer cells. In this study, we investigated the role of TRPC6 in cell cycle progression and in the development of human glioma. TRPC6 protein and mRNA expression were assessed in glioma (n = 33) and normal (n = 17) brain tissues from patients and in human glioma cell lines U251, U87, and T98G. Activation of TRPC6 channels was tested by platelet-derived growth factor-induced Ca(2+) imaging. The effect of inhibiting TRPC6 activity or expression using the dominant-negative mutant TRPC6 (DNC6) or RNA interference, respectively, was tested on cell growth, cell cycle progression, radiosensitization of glioma cells, and development of xenografted human gliomas in a mouse model. The green fluorescent protein (GFP) and wild-type TRPC6 (WTC6) were used as controls. Survival of mice bearing xenografted tumors in the GFP, DNC6, and WTC6 groups (n = 13, 15, and 13, respectively) was compared using Kaplan-Meier analysis. All statistical tests were two-sided. Functional TRPC6 was overexpressed in human glioma cells. Inhibition of TRPC6 activity or expression attenuated the increase in intracellular Ca(2+) by platelet-derived growth factor, suppressed cell growth and clonogenic ability, induced cell cycle arrest at the G2/M phase, and enhanced the antiproliferative effect of ionizing radiation. Cyclin-dependent kinase 1 activation and cell division cycle 25 homolog C expression regulated the cell cycle arrest. Inhibition of TRPC6 activity also reduced tumor volume in a subcutaneous mouse model of xenografted human tumors (P = .014 vs GFP; P < .001 vs WTC6) and increased mean survival in mice in an intracranial model (P < .001 vs GFP or WTC6). In this preclinical model, TRPC6 channels were essential for glioma development via regulation of G2/M phase transition. This study suggests that TRPC6 might be a new target for therapeutic intervention of human glioma.
学科主题Oncology
收录类别SCI
资助信息973 Program[2006CB806600]; National Natural Science Foundation of China[30711120566]
语种英语
公开日期2012-07-13
源URL[http://ir.sibs.ac.cn/handle/331001/1584]  
专题上海神经科学研究所_神经所(总)
上海神经科学研究所_神经信号转导研究组
推荐引用方式
GB/T 7714
Wang, Yizheng,Yao, Hailan. Essential Role of TRPC6 Channels in G2/M Phase Transition and Development of Human Glioma[J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE,2010,102(14):1052-1068.
APA Wang, Yizheng,&Yao, Hailan.(2010).Essential Role of TRPC6 Channels in G2/M Phase Transition and Development of Human Glioma.JOURNAL OF THE NATIONAL CANCER INSTITUTE,102(14),1052-1068.
MLA Wang, Yizheng,et al."Essential Role of TRPC6 Channels in G2/M Phase Transition and Development of Human Glioma".JOURNAL OF THE NATIONAL CANCER INSTITUTE 102.14(2010):1052-1068.

入库方式: OAI收割

来源:上海神经科学研究所

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