Targeting calcium signaling in cancer therapy

被引:415
作者
Cui, Chaochu [1 ,2 ,3 ]
Merritt, Robert [3 ,4 ]
Fu, Liwu [1 ,2 ]
Pan, Zui [3 ,4 ,5 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol South China, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Ctr Canc, Collaborat Innovat Ctr Canc Med, Guangzhou 510060, Guangdong, Peoples R China
[3] Ohio State Univ, Dept Surg, Div Thorac Dis, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[5] Univ Texas Arlington, Coll Nursing & Hlth Innovat, LS Bldg 239,501 S Nedderman Dr, Arlington, TX 76019 USA
关键词
Ca2+ channels; Store-operated Ca2+ entry; Cell proliferation; Migration; Apoptosis; Channel blockers; Cancer therapy; ACTIVATED CA2+ CHANNELS; SQUAMOUS-CELL CARCINOMA; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; POTENTIAL VANILLOID-1 TRPV1; HUMAN OVARIAN-CANCER; HUMAN COLON-CANCER; MOLECULE; STIM2; BREAST-CANCER; PROSTATE-CANCER; ION-CHANNEL;
D O I
10.1016/j.apsb.2016.11.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The intracellular calcium ions (Ca2+) act as second messenger to regulate gene transcription, cell proliferation, migration and death. Accumulating evidences have demonstrated that intracellular Ca2+ homeostasis is altered in cancer cells and the alteration is involved in tumor initiation, angiogenesis, progression and metastasis. Targeting derailed Ca2+ signaling for cancer therapy has become an emerging research area. This review summarizes some important Ca2+ channels, transporters and Ca2+-ATPases, which have been reported to be altered in human cancer patients. It discusses the current research effort toward evaluation of the blockers, inhibitors or regulators for Ca2+ channels/transporters or Ca2+-ATPase pumps as anti-cancer drugs. This review is also aimed to stimulate interest in, and support for research
引用
收藏
页码:3 / 17
页数:15
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