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抑癌基因 Par-4 诱导细胞凋亡的机制。

Mechanisms of apoptosis by the tumor suppressor Par-4.

机构信息

Graduate Center for Toxicology, University of Kentucky, Lexington, Kentucky 40536, USA.

出版信息

J Cell Physiol. 2012 Dec;227(12):3715-21. doi: 10.1002/jcp.24098.

Abstract

Par-4 is a pro-apoptotic, tumor suppressor protein that induces apoptosis selectively in cancer cells. Endoplasmic reticulum-stress and higher levels of protein kinase A in tumor cells confer the coveted feature of cancer selective response to extracellular and intracellular Par-4, respectively. Recent studies have shown that systemic Par-4 confers resistance to tumor growth in mice, and that tumor-resistance is transferable by bone-marrow transplantation. Moreover, recombinant Par-4 inhibits the growth of tumors in mice. As systemic Par-4 induces apoptosis via cell surface GRP78, strategies that promote GRP78 trafficking to the cell surface are expected sensitize cancer cells to circulating levels of Par-4. This review illustrates the domains and mechanisms by which Par-4 orchestrates the apoptotic process in both cell culture models and in physiological settings.

摘要

Par-4 是一种促凋亡的肿瘤抑制蛋白,它选择性地诱导癌细胞凋亡。内质网应激和肿瘤细胞中蛋白激酶 A 的更高水平分别赋予了细胞外和细胞内 Par-4 对癌细胞具有令人垂涎的选择性反应的特征。最近的研究表明,系统 Par-4 赋予了小鼠对肿瘤生长的抗性,并且通过骨髓移植可以转移肿瘤抗性。此外,重组 Par-4 抑制了小鼠肿瘤的生长。由于系统 Par-4 通过细胞表面 GRP78 诱导细胞凋亡,因此预计促进 GRP78 向细胞表面转运的策略将使癌细胞对循环水平的 Par-4 敏感。这篇综述说明了 Par-4 在细胞培养模型和生理环境中协调细胞凋亡过程的结构域和机制。

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