High expression of SNIP1 correlates with poor prognosis in Non-small cell lung cancer and SNIP1 interferes with the recruitment of HDAC1 to RB in vitro

被引:11
|
作者
Jeon, Hyo-Sung [1 ]
Choi, Yi Young [1 ]
Fukuoka, Junya [2 ]
Fujii, Makiko [3 ]
Lyakh, Lyudmila A. [4 ]
Song, Sang-Hyun [5 ]
Travis, William D. [6 ]
Park, Jae Yong [1 ]
Jen, Jin [7 ]
机构
[1] Kyungpook Natl Univ, Sch Med, Dept Biochem & Cell Biol, Taegu 700422, South Korea
[2] Toyama Univ Hosp, Toyama Tissue Microarray Lab, Anat Pathol Lab, Toyama 9300194, Japan
[3] Aichi Canc Ctr, Res Inst, Div Mol Oncol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[4] NCI, Canc & Inflammat Program, Ctr Canc Res, Frederick, MD 21702 USA
[5] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul, South Korea
[6] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[7] Mayo Clin, Dept Med, Div Pulm & Crit Care Med, Rochester, MN 55905 USA
基金
新加坡国家研究基金会;
关键词
SNIP1; RB; HDAC1; Prognosis; Lung cancer; RETINOBLASTOMA PROTEIN; HISTONE DEACETYLASE; REPRESS TRANSCRIPTION; DOMAIN; CYCLE;
D O I
10.1016/j.lungcan.2013.07.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Rb tumor suppressor gene performs a critical role in controlling cell proliferation and tumorigenesis; it recruits HDAC1 protein into the E2F complexes to repress transcription. In this study, we demonstrate that SNIP1, RB and HDAC1 were significantly expressed in same lung cancer tissues in a tissue microarray (TMA) containing 300 non-small cell lung cancers (NSCLC). High expression level of SNIP) in tumor patients was significantly correlated with poor prognosis in NSCLC (log-rank P for OS = 0.01, log-rank P for DFS = 0.001). Functionally, SNIP1 competes with HDAC1 for binding to RB and reduces HDAC activity in vitro. Knockdown of SNIP1 reduced colony formation ability of lung cancer cells. These findings may indicate the involvement of SNIP1 in progression of lung cancer by regulating the RB/HDAC1 interaction. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:24 / 30
页数:7
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