Comparison of the protein expression of calpain-1, calpain-2, calpastatin and calmodulin between gastric cancer and normal gastric mucosa

被引:15
作者
Liu, Bide [1 ]
Zhou, Yu [1 ]
Lu, Dan [2 ,3 ]
Liu, Yong [4 ]
Zhang, Si-Quan [1 ]
Xu, Yan [2 ]
Li, Wei [1 ,3 ]
Gu, Xiao [2 ,3 ]
机构
[1] Yangzhou Univ, Coll Med, 11 Huaihai Rd, Yangzhou 225001, Jiangsu, Peoples R China
[2] Yangzhou Univ, Coll Clin Med, 11 Huaihai Rd, Yangzhou 225001, Jiangsu, Peoples R China
[3] Jiangsu Key Lab Integrated Tradit Chinese & Weste, Yangzhou 225001, Jiangsu, Peoples R China
[4] Dalian Univ Technol, Sch Life Sci & Med, Panjin 124221, Liaoning, Peoples R China
关键词
gastric cancer; calpain-1; calpain-2; calpastatin; calmodulin; PEST SEQUENCES; SECRETION; CLEAVAGE; PROSTATE; SYSTEM; OVEREXPRESSION; ACTIVATION; SURVIVAL;
D O I
10.3892/ol.2017.6617
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The understanding of molecular mechanisms that are involved in the development and the progression of gastric cancer (GC) are of importance for the diagnosis and treatment. The calpain system, which contains the calpains and the endogenous inhibitor, has been suggested as an important factor in the tumorigenesis and migration of colorectal adenocarcinoma, breast and ovarian cancer, and as a prognostic marker for GC. However, the expression level of calpain system proteins in GC and normal-appearing peritumoral gastric mucosa remain unknown. The present study investigated the expression of calpain-1 (CAPN1), calpain-2 (CAPN2), calpastatin and calmodulin (CaM) in GC and uninvolved gastric mucosa tissues with immunohistochemistry. Results demonstrated that CAPN2 protein level increased in GCs compared with normal tissues, while calpastatin and CaM protein level decreased. No evident alterations were observed for CAPN1. Although the protein expression of all these four proteins was not in association with the clinical variables of GC in the present study, higher calpain enzyme activity could be a negative prognostic marker, since calpains are responsible for the generation of active forms of certain proteins that facilitate the progression of cancer. The ratio of (CAPN1 x CAPN2)/(calpastatin x CaM) may serve as a potential index for diagnosis of GC.
引用
收藏
页码:3705 / 3710
页数:6
相关论文
共 29 条
[1]   PEST SEQUENCES IN CALMODULIN-BINDING PROTEINS [J].
BARNES, JA ;
GOMES, AV .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 149 :17-27
[2]   Calpain: a role in cell transformation and migration [J].
Carragher, NO ;
Frame, MC .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2002, 34 (12) :1539-1543
[3]   Annual report on status of cancer in China, 2011 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Zeng, Hongmei ;
Zhang, Siwei ;
He, Jie .
CHINESE JOURNAL OF CANCER RESEARCH, 2015, 27 (01) :2-12
[4]   Inhibition of calpain blocks platelet secretion, aggregation, and spreading [J].
Croce, K ;
Flaumenhaft, R ;
Rivers, M ;
Furie, B ;
Furie, BC ;
Herman, IM ;
Potter, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36321-36327
[5]   The calpain family and human disease [J].
Huang, YH ;
Wang, KKW .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (08) :355-362
[6]   Selenoprotein K Is a Novel Target of m-Calpain, and Cleavage Is Regulated by Toll-like Receptor-induced Calpastatin in Macrophages [J].
Huang, Zhi ;
Hoffmann, Fukun W. ;
Norton, Robert L. ;
Hashimoto, Ann C. ;
Hoffmann, Peter R. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (40) :34830-34838
[7]   Chymotrypsin-Like Activity of Proteasomes and Total Calpain Activity in Gastric and Colorectal Cancer [J].
Ivanova, E. V. ;
Kondakova, I. V. ;
Spirina, L. V. ;
Afanas'ev, S. G. ;
Avgustinovich, A. V. ;
Cheremisina, O. V. .
BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE, 2014, 157 (06) :781-784
[8]  
Lakshmikuttyamma A, 2004, CANCER EPIDEM BIOMAR, V13, P1604
[9]   Over-expression of calpastatin inhibits calpain activation and attenuates myocardial dysfunction during endotoxaemia [J].
Li, Xiaoping ;
Li, Ying ;
Shan, Limei ;
Shen, E. ;
Chen, Ruizhen ;
Peng, Tianqing .
CARDIOVASCULAR RESEARCH, 2009, 83 (01) :72-79
[10]   Evidence for calpain-mediated androgen receptor cleavage as a mechanism for androgen independence [J].
Libertini, Stephen J. ;
Tepper, Clifford G. ;
Rodriguez, Veronica ;
Asmuth, David M. ;
Kung, Hsing-Jien ;
Mudryj, Maria .
CANCER RESEARCH, 2007, 67 (19) :9001-9005