Durham A C, Walton J M
Biosci Rep. 1982 Jan;2(1):15-30. doi: 10.1007/BF01142195.
Several lines of evidence suggest tha Ca2+ ions control cell proliferation: Ca2+ entry into cytoplasm acts as a general mitogen; serum and serum-replacements induce Ca2+ influx; the Ca2+ concentrations in growth media required to support the proliferation of normal cells are much higher than those required for cancer cells; serum and growth factors reduce the Ca2+ requirements of normal cells; tumour promoters alter Ca2+ fluxes via a mechanism used principally by growth factors. Minor supporting evidence includes the effects of various drugs and viruses, and the behaviour of tumour cell mitochondria and intercellular junctions. It is still not possible to decide exactly where and when inside cells the critical effect of Ca2+ on proliferation occurs, but we discuss at length the practical problems of understanding Ca2+ movements in tissue-culture cells. Carried to its logical conclusion, present evidence suggests that an overridden or bypassed Ca2+ control process may be the key, common determinant of unrestrained proliferation in cancer cells.
钙离子进入细胞质起着通用促有丝分裂原的作用;血清和血清替代物诱导钙离子内流;支持正常细胞增殖所需的生长培养基中的钙离子浓度远高于癌细胞所需的浓度;血清和生长因子降低了正常细胞对钙离子的需求;肿瘤启动子通过主要由生长因子使用的机制改变钙离子通量。次要的支持证据包括各种药物和病毒的作用,以及肿瘤细胞线粒体和细胞间连接的行为。目前仍无法确切确定钙离子对增殖的关键作用在细胞内何处以及何时发生,但我们详细讨论了理解组织培养细胞中钙离子运动的实际问题。从逻辑上推断,现有证据表明,一个被超越或绕过的钙离子控制过程可能是癌细胞不受限制增殖的关键共同决定因素。