Gregory R. Monteith,D. McAndrew,Helen M. Faddy,Sarah J. Roberts-Thomson
出处
期刊:Nature Reviews Cancer [Springer Nature] 日期:2007-07-01卷期号:7 (7): 519-530被引量:508
标识
DOI:10.1038/nrc2171
摘要
Ca2+ is a ubiquitous cellular signal. Altered expression of specific Ca2+ channels and pumps are characterizing features of some cancers. The ability of Ca2+ to regulate both cell death and proliferation, combined with the potential for pharmacological modulation, offers the opportunity for a set of new drug targets in cancer. However, the ubiquity of the Ca2+ signal is often mistakenly presumed to thwart the specific therapeutic targeting of proteins that transport Ca2+. This Review presents evidence to the contrary and addresses the question: which Ca2+ channels and pumps should be targeted?