Institut Gustave Roussy Cancer Campus, Villejuif, France; Université Paris Descartes, Sorbonne Paris Cité, Paris, France; Equipe 11 labellisée Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, Paris, France; Institut National de la Santé et de la Recherche Médicale, U1138, Paris, France; Université Pierre et Marie Curie, Paris, France; Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Campus, Villejuif, France; Faculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, France.
Université Paris Descartes, Sorbonne Paris Cité, Paris, France; Equipe 11 labellisée Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, Paris, France; Institut National de la Santé et de la Recherche Médicale, U1138, Paris, France; Université Pierre et Marie Curie, Paris, France.
Cell Calcium. 2018 Mar;70:3-15. doi: 10.1016/j.ceca.2017.07.006. Epub 2017 Jul 25.
Cytosolic Ca concentration levels fluctuate in an ordered manner along the cell cycle, in line with the fact that Ca is involved in the regulation of cell proliferation. Cell proliferation should be an error-free process, yet is endangered by mistakes. In fact, a complex network of proteins ensures that cell cycle does not progress until the previous phase has been successfully completed. Occasionally, errors occur during the cell cycle leading to cell cycle arrest. If the error is severe, and the cell cycle checkpoints work perfectly, this results into cellular demise by activation of apoptotic or non-apoptotic cell death programs. Cancer is characterized by deregulated proliferation and resistance against cell death. Ca is a central key to these phenomena as it modulates signaling pathways that control oncogenesis and cancer progression. Here, we discuss how Ca participates in the exogenous and endogenous signals controlling cell proliferation, as well as in the mechanisms by which cells die if irreparable cell cycle damage occurs. Moreover, we summarize how Ca homeostasis remodeling observed in cancer cells contributes to deregulated cell proliferation and resistance to cell death. Finally, we discuss the possibility to target specific components of Ca signal pathways to obtain cytostatic or cytotoxic effects.
细胞质 Ca 浓度水平沿着细胞周期呈有序波动,这与 Ca 参与细胞增殖调节的事实一致。细胞增殖应该是一个无差错的过程,但却面临着错误的威胁。事实上,一个复杂的蛋白质网络确保细胞周期在先前的阶段成功完成之前不会进展。偶尔,细胞周期中会出现错误,导致细胞周期停滞。如果错误严重,并且细胞周期检查点完美运作,这将导致细胞凋亡或非凋亡性细胞死亡程序的激活而导致细胞死亡。癌症的特征是增殖失控和对细胞死亡的抵抗。Ca 是这些现象的核心关键,因为它调节控制致癌和癌症进展的信号通路。在这里,我们讨论 Ca 如何参与控制细胞增殖的外源性和内源性信号,以及在不可修复的细胞周期损伤发生时细胞死亡的机制。此外,我们总结了在癌细胞中观察到的 Ca 动态平衡重塑如何导致增殖失控和对细胞死亡的抵抗。最后,我们讨论了靶向 Ca 信号通路特定成分以获得细胞抑制或细胞毒性作用的可能性。