中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Ras-induced Epigenetic Inactivation of the RRAD ( Ras-related Associated with Diabetes) Gene Promotes Glucose Uptake in a Human Ovarian Cancer Model

文献类型:期刊论文

作者Wang, Yan1,2; Li, Guiling3; Mao, Fengbiao2,4; Li, Xianfeng5; Liu, Qi3; Chen, Lin4; Lv, Lu3; Wang, Xin3; Wu, Jinyu3; Dai, Wei1
刊名JOURNAL OF BIOLOGICAL CHEMISTRY
出版日期2014-05-16
卷号289期号:20页码:14225-14238
关键词DNA Methylation Metabolism Ovarian Cancer Ras Tumor Suppressor Gene Oncogenic Transformation RRAD
ISSN号0021-9258
英文摘要Background: Increased glucose uptake is essential for carcinogenesis. Results: Ras(V12)-induced epigenetic inactivation of RRAD promotes glucose uptake and tumor formation. Conclusion: RRAD might act as a functional tumor suppressor by inhibiting glucose uptake. Significance: Down-regulation of RRAD in tumor tissues might be associated with the Warburg effect. RRAD (Ras-related associated with diabetes) is a small Ras-related GTPase that is frequently inactivated by DNA methylation of the CpG island in its promoter region in cancer tissues. However, the role of the methylation-induced RRAD inactivation in tumorigenesis remains unclear. In this study, the Ras-regulated transcriptome and epigenome were profiled by comparing T29H (a Ras(V12)-transformed human ovarian epithelial cell line) with T29 (an immortalized but non-transformed cell line) through reduced representation bisulfite sequencing and digital gene expression. We found that Ras(V12)-mediated oncogenic transformation was accompanied by RRAD promoter hypermethylation and a concomitant loss of RRAD expression. In addition, we found that the RRAD promoter was hypermethylated, and its transcription was reduced in ovarian cancer versus normal ovarian tissues. Treatment with the DNA methyltransferase inhibitor 5-aza-2-deoxycytidine resulted in demethylation in the RRAD promoter and restored RRAD expression in T29H cells. Additionally, treatment with farnesyltransferase inhibitor FTI277 resulted in restored RRAD expression and inhibited DNA methytransferase expression and activity in T29H cells. By employing knockdown and overexpression techniques in T29 and T29H, respectively, we found that RRAD inhibited glucose uptake and lactate production by repressing the expression of glucose transporters. Finally, RRAD overexpression in T29H cells inhibited tumor formation in nude mice, suggesting that RRAD is a tumor suppressor gene. Our results indicate that Ras(V12)-mediated oncogenic transformation induces RRAD epigenetic inactivation, which in turn promotes glucose uptake and may contribute to ovarian cancer tumorigenesis.
收录类别SCI
语种英语
WOS记录号WOS:000335984600048
源URL[http://ir.psych.ac.cn/handle/311026/13492]  
专题心理研究所_健康与遗传心理学研究室
作者单位1.Chinese Acad Sci, Inst Psychol, Beijing 100101, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100080, Peoples R China
3.Wenzhou Med Univ, Inst Genom Med, Wenzhou 325000, Zhejiang, Peoples R China
4.Chinese Acad Sci, Beijing Inst Life Sci, Beijing 100101, Peoples R China
5.Cent S Univ, State Key Lab Med Genet, Changsha 410078, Hunan, Peoples R China
6.Chinese Peoples Liberat Army, Gen Hosp, Dept Obstet & Gynecol, Beijing 100853, Peoples R China
推荐引用方式
GB/T 7714
Wang, Yan,Li, Guiling,Mao, Fengbiao,et al. Ras-induced Epigenetic Inactivation of the RRAD ( Ras-related Associated with Diabetes) Gene Promotes Glucose Uptake in a Human Ovarian Cancer Model[J]. JOURNAL OF BIOLOGICAL CHEMISTRY,2014,289(20):14225-14238.
APA Wang, Yan.,Li, Guiling.,Mao, Fengbiao.,Li, Xianfeng.,Liu, Qi.,...&Sun, Zhong Sheng.(2014).Ras-induced Epigenetic Inactivation of the RRAD ( Ras-related Associated with Diabetes) Gene Promotes Glucose Uptake in a Human Ovarian Cancer Model.JOURNAL OF BIOLOGICAL CHEMISTRY,289(20),14225-14238.
MLA Wang, Yan,et al."Ras-induced Epigenetic Inactivation of the RRAD ( Ras-related Associated with Diabetes) Gene Promotes Glucose Uptake in a Human Ovarian Cancer Model".JOURNAL OF BIOLOGICAL CHEMISTRY 289.20(2014):14225-14238.

入库方式: OAI收割

来源:心理研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。