Prognostic value of regulator of G-protein signaling 6 in colorectal cancer

被引:10
作者
Luo, Yang [1 ]
Qin, Shao-Lan [1 ]
Yu, Min-Hao [1 ]
Mu, Yi-Fei [1 ]
Wang, Zheng-Shi [1 ]
Zhong, Ming [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Gastrointestinal Surg, Shanghai 200127, Peoples R China
关键词
RGS6; Colorectal cancer; Metastasis; Prognosis; GTPASE-ACTIVATING PROTEINS; POOR-PROGNOSIS; RGS PROTEINS; EXPRESSION; APOPTOSIS;
D O I
10.1016/j.biopha.2015.10.012
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Reprogrammed metabolism is a hallmark of cancer cells. Regulator of G-protein signaling 6 (RGS6), which is frequently down-regulated in multiple human malignancies, has been demonstrated to play a critical function in energy metabolism, cell apoptosis and tumorigenesis. However, limited knowledge is known about the expression pattern and prognostic value of RGS6 in colorectal cancer (CRC). In this study, we first observed that RGS6 mRNA and protein is commonly downregulated in 32 paired CRC tissues compared with their normal counterparts. Furthermore, by a large scale of immunohistochemical analysis in a tissue microarray containing 310 cases of CRC specimens, we demonstrated that the protein expression of RGS6 expression is downregulated in 40.97% (127/310) samples and detected that decreasing RGS6 expression is closely correlated with enhanced tumor size, CEA level, T classification, TNM stage, and easier lymphatic and distant metastasis. Meanwhile, Kaplan-Meier survival analysis showed that CRC patients with a lower RGS6 expression have a poorer clinical outcome than those with a higher RGS6 expression. Multivariate Cox regression analysis revealed that RGS6, lymphatic metastasis and distant metastasis are the independent prognostic factors for overall survival rate of CRC patients. Taken together, our studies reveal the prognostic value of RGS6 in CRC and support that RGS6 may act as a molecular target for CRC treatment. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:147 / 152
页数:6
相关论文
共 20 条
[11]  
Jiang N, 2014, INT J CLIN EXP PATHO, V7, P4120
[12]  
Liu Z., 2004, J BIOL CHEM, V279
[13]   Regulator of G protein signaling 6 is a novel suppressor of breast tumor initiation and progression [J].
Maity, Biswanath ;
Stewart, Adele ;
OMalley, Yunxia ;
Askeland, Ryan W. ;
Sugg, Sonia L. ;
Fisher, Rory A. .
CARCINOGENESIS, 2013, 34 (08) :1747-1755
[14]   Regulator of G Protein Signaling 6 (RGS6) Induces Apoptosis via a Mitochondrial-dependent Pathway Not Involving Its GTPase-activating Protein Activity [J].
Maity, Biswanath ;
Yang, Jianqi ;
Huang, Jie ;
Askeland, Ryan W. ;
Bera, Soumen ;
Fisher, Rory A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (02) :1409-1419
[15]   R7BP, a novel neuronal protein interacting with RGS proteins of the R7 family [J].
Martemyanov, KA ;
Yoo, PJ ;
Skiba, NP ;
Arshavsky, VY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (07) :5133-5136
[16]   GTPase-activating proteins for heterotrimeric G proteins: Regulators of G protein signaling (RGS) and RGS-like proteins [J].
Ross, EM ;
Wilkie, TM .
ANNUAL REVIEW OF BIOCHEMISTRY, 2000, 69 :795-827
[17]  
Siegel R, 2014, CA-CANCER J CLIN, V64, P104, DOI [10.3322/caac.21395, 10.3322/caac.21220]
[18]  
Wang ZS, 2014, INT J CLIN EXP PATHO, V7, P8077
[19]   G-protein Inactivator RGS6 Mediates Myocardial Cell Apoptosis and Cardiomyopathy Caused By Doxorubicin [J].
Yang, Jianqi ;
Maity, Biswanath ;
Huang, Jie ;
Gao, Zhan ;
Stewart, Adele ;
Weiss, Robert M. ;
Anderson, Mark E. ;
Fisher, Rory A. .
CANCER RESEARCH, 2013, 73 (06) :1662-1667
[20]   Epidemiology of colorectal cancer in Asia [J].
Yee, Yuk Kei ;
Tan, Victoria P. Y. ;
Chan, Pierre ;
Hung, Ivan F. N. ;
Pang, Roberta ;
Wong, Benjamin C. Y. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2009, 24 (12) :1810-1816