Wu Zengding, Wang Guanlin, Zhang Kuanren
Lab of Molecular Pharmacology, Kunming University of Science and Technology, Kunming 650500, China. E-mail:
Nan Fang Yi Ke Da Xue Xue Bao. 2014 Jan;34(1):128-32.
As a pro-apoptotic factor, prostate apoptosis response protein 4 (par-4) was first found in the male hormone-dependent prostate cells (AT-3). Endogenous Par-4 sensitizes cancer cells to apoptotic stimuli, but exogenous Par-4 selectively induces apoptosis in cancer cells, and these activities depends on the structure of its core domain SAC. Par-4 and SAC can specifically induce apoptosis of cancer cells but not of normal cells, and are therefore potential anti-cancer drugs. In this review we summarize the discovery, structure, and function of par-4, and its intracellular signaling pathways, then discuss the application prospects of Par-4 and SAC in the clinical treatment of cancer and the problems in its research and clinical applications.
作为一种促凋亡因子,前列腺凋亡反应蛋白4(Par-4)最初在雄激素依赖的前列腺细胞(AT-3)中被发现。内源性Par-4使癌细胞对凋亡刺激敏感,而外源性Par-4则选择性地诱导癌细胞凋亡,且这些活性取决于其核心结构域SAC的结构。Par-4和SAC可特异性诱导癌细胞而非正常细胞凋亡,因此是潜在的抗癌药物。在本综述中,我们总结了Par-4的发现、结构和功能及其细胞内信号通路,然后讨论了Par-4和SAC在癌症临床治疗中的应用前景以及其研究和临床应用中存在的问题。