CAPN6 in disease: An emerging therapeutic target (Review)

被引:15
作者
Chen, Lin [1 ,2 ]
Xiao, Dongqiong [1 ,2 ]
Tang, Fajuan [1 ,2 ]
Gao, Hu [1 ,2 ]
Li, Xihong [1 ,2 ]
机构
[1] Sichuan Univ, West China Univ Hosp 2, Dept Emergency Med, 20,Sect 3,Renmin South Rd, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, Minist Educ, Key Lab Birth Defects & Related Dis Women & Child, Chengdu 610041, Sichuan, Peoples R China
基金
美国国家科学基金会;
关键词
calpain6; cell proliferation; apoptosis; therapeutic target; DIFFERENTIAL GENE-EXPRESSION; CALPAIN PROTEOLYTIC SYSTEMS; MESSENGER-RNA; ENDOTHELIAL-CELLS; INDUCED APOPTOSIS; DOWN-REGULATION; CANCER; ROLES; IDENTIFICATION; INHIBITION;
D O I
10.3892/ijmm.2020.4734
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
As a member of the calpain protein family, calpain6 (CAPN6) is highly expressed mainly in the placenta and embryos. It plays a number of important roles in cellular processes, such as the stabilization of microtubules, the maintenance of cell stability, the control of cell movement and the inhibition of apoptosis. In recent years, various studies have found that CAPN6 is one of the contributing factors associated with the tumorigenesis of uterine tumors and osteosarcoma, and that CAPN6 participates in the development of tumors by promoting cell proliferation and angiogenesis, and by inhibiting apoptosis, which is mainly regulated by the phosphatidylinositol 3 kinase (PI3K)/protein kinase B (Akt) pathway. Due to its abnormal cellular expression, CAPN6 has also been found to be associated with a number of diseases, such as white matter damage and muscular dystrophy. Therefore, CAPN6 may be a novel therapeutic target for these diseases. In the present review, the role of CAPN6 in disease and its possible use as a target in various therapies are discussed.
引用
收藏
页码:1644 / 1652
页数:9
相关论文
共 87 条
[21]   Cluster analysis and phylogenetic relationship in biomarker identification of type 2 diabetes and nephropathy [J].
Guttula, Satya Vani ;
Rao, Allam Appa ;
Sridhar, G. R. ;
Chakravarthy, M. S. ;
Nageshwararo, Kunjum ;
Rao, Paturi V. .
INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES, 2010, 30 (01) :52-56
[22]   Calcium-bound structure of calpain and its mechanism of inhibition by calpastatin [J].
Hanna, Rachel A. ;
Campbell, Robert L. ;
Davies, Peter L. .
NATURE, 2008, 456 (7220) :409-U78
[23]   The physiological response of protease inhibition in dystrophic muscle [J].
Hollinger, K. ;
Selsby, J. T. .
ACTA PHYSIOLOGICA, 2013, 208 (03) :234-244
[24]   Calpain-6, a Target Molecule of Glucocorticoids, Regulates Osteoclastic Bone Resorption via Cytoskeletal Organization and Microtubule Acetylation [J].
Hong, Jung Min ;
Teitelbaum, Steven L. ;
Kim, Tae-Ho ;
Ross, F. Patrick ;
Kim, Shin-Yoon ;
Kim, Hyun-Ju .
JOURNAL OF BONE AND MINERAL RESEARCH, 2011, 26 (03) :657-665
[25]  
Hosseini M, 2018, ARCH IRAN MED, V21, P170
[26]   Roles of the PI-3K and MEK pathways in Ras-mediated chemoresistance in breast cancer cells [J].
Jin, W ;
Wu, L ;
Liang, K ;
Liu, B ;
Lu, Y ;
Fan, Z .
BRITISH JOURNAL OF CANCER, 2003, 89 (01) :185-191
[27]  
Kaci I, 2013, J BONE MINER RES, V28
[28]   Receptor-Independent Cardiac Protein Kinase Cα Activation by Calpain-Mediated Truncation of Regulatory Domains [J].
Kang, Min-Young ;
Zhang, Yan ;
Matkovich, Scot J. ;
Diwan, Abhinav ;
Chishti, Athar H. ;
Dorn, Gerald W., II .
CIRCULATION RESEARCH, 2010, 107 (07) :903-912
[29]   Calpain involvement in the remodeling of cytoskeletal anchorage complexes [J].
Lebart, Marie-Christine ;
Benyamin, Yves .
FEBS JOURNAL, 2006, 273 (15) :3415-3426
[30]   Increased expression of calpain 6 in uterine sarcomas and carcinosarcomas: an immunohistochemical analysis [J].
Lee, S. -J. ;
Choi, Y. -L. ;
Lee, E. -J. ;
Kim, B. -G. ;
Bae, D. -S. ;
Ahn, G. H. ;
Lee, J. -H. .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2007, 17 (01) :248-253