NDRG4 is Downregulated in Glioblastoma and Inhibits Cell Proliferation

被引:25
作者
Ding, Wenchao [2 ]
Zhang, Jing [1 ,2 ]
Yoon, Jae-Geun [1 ]
Shi, Dongyan [3 ]
Foltz, Gregory [1 ]
Lin, Biaoyang [1 ,2 ,3 ,4 ]
机构
[1] Swedish Med Ctr, Swedish Neurosci Inst, Seattle, WA 98122 USA
[2] Zhejiang Univ, Zhejiang Calif Int Nanosyst Inst ZCNI, Syst Biol Div, Hangzhou 310003, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, Hangzhou 310003, Zhejiang, Peoples R China
[4] Univ Washington, Dept Urol, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
COLORECTAL-CANCER; GENE; EXPRESSION; MYC; SUPPRESSOR; CARCINOMA; CYCLE;
D O I
10.1089/omi.2011.0146
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
NDRG4 is a member of the N-myc downregulated gene family (NDRG) belonging to the alpha/beta hydrolase superfamily. We have previously documented discrepancy between our analysis of the expression and function of NDRG4 in glioblastoma multiforme (GBM) and a recent publication by Schilling et al., who reported that NDRG4 is upregulated in GBM compared to human cortex tissues and knock down of NDRG4 reduced the viability of GBM cells. In the present study, we found that NDRG4 is indeed downregulated, at both RNA and protein levels, by quantitative RT-PCR and Western blot analysis, in GBM compared to normal tissues, and that over expression of NDRG4 inhibited proliferation of GBM cells. These new observations can inform the selection of lead molecular compounds for drug discovery as well as novel diagnostics for GBM. They also lend evidence to NDRG4 a role of tumor suppressor.
引用
收藏
页码:263 / 267
页数:5
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