Suppr超能文献

肿瘤抑制因子Par-4激活细胞凋亡的一条外在途径。

The tumor suppressor Par-4 activates an extrinsic pathway for apoptosis.

作者信息

Burikhanov Ravshan, Zhao Yanming, Goswami Anindya, Qiu Shirley, Schwarze Steven R, Rangnekar Vivek M

机构信息

Department of Radiation Medicine, University of Kentucky, Lexington, KY 40536, USA.

出版信息

Cell. 2009 Jul 23;138(2):377-88. doi: 10.1016/j.cell.2009.05.022.

Abstract

Prostate apoptosis response-4 (Par-4) is a proapoptotic protein with intracellular functions in the cytoplasm and nucleus. Unexpectedly, we noted Par-4 protein is spontaneously secreted by normal and cancer cells in culture, and by Par-4 transgenic mice that are resistant to spontaneous tumors. Short exposure to endoplasmic reticulum (ER) stress-inducing agents further increased cellular secretion of Par-4 by a brefeldin A-sensitive pathway. Secretion occurred independently of caspase activation and apoptosis. Interestingly, extracellular Par-4 induced apoptosis by binding to the stress response protein, glucose-regulated protein-78 (GRP78), expressed at the surface of cancer cells. The interaction of extracellular Par-4 and cell surface GRP78 led to apoptosis via ER stress and activation of the FADD/caspase-8/caspase-3 pathway. Moreover, apoptosis inducible by TRAIL, which also exerts cancer cell-specific effects, is dependent on extracellular Par-4 signaling via cell surface GRP78. Thus, Par-4 activates an extrinsic pathway involving cell surface GRP78 receptor for induction of apoptosis.

摘要

前列腺凋亡反应蛋白4(Par-4)是一种在细胞质和细胞核中具有细胞内功能的促凋亡蛋白。出乎意料的是,我们发现Par-4蛋白在培养的正常细胞和癌细胞以及对自发性肿瘤具有抗性的Par-4转基因小鼠中会自发分泌。短期暴露于内质网(ER)应激诱导剂会通过布雷菲德菌素A敏感途径进一步增加细胞对Par-4的分泌。分泌过程独立于半胱天冬酶激活和凋亡。有趣的是,细胞外的Par-4通过与癌细胞表面表达的应激反应蛋白葡萄糖调节蛋白78(GRP78)结合来诱导凋亡。细胞外Par-4与细胞表面GRP78的相互作用通过内质网应激和FADD/半胱天冬酶-8/半胱天冬酶-3途径的激活导致凋亡。此外,TRAIL诱导的凋亡(TRAIL也具有癌细胞特异性作用)依赖于通过细胞表面GRP78的细胞外Par-4信号传导。因此,Par-4激活了一条涉及细胞表面GRP78受体的外在途径来诱导凋亡。

相似文献

1
The tumor suppressor Par-4 activates an extrinsic pathway for apoptosis.
Cell. 2009 Jul 23;138(2):377-88. doi: 10.1016/j.cell.2009.05.022.
2
The Par-4-GRP78 TRAIL, more twists and turns.
Cancer Biol Ther. 2009 Nov;8(22):2103-5. doi: 10.4161/cbt.8.22.10140. Epub 2009 Nov 20.
3
Mechanisms of apoptosis by the tumor suppressor Par-4.
J Cell Physiol. 2012 Dec;227(12):3715-21. doi: 10.1002/jcp.24098.
6
Novel mechanism of apoptosis resistance in cancer mediated by extracellular PAR-4.
Cancer Res. 2013 Jan 15;73(2):1011-9. doi: 10.1158/0008-5472.CAN-12-3212. Epub 2012 Nov 30.
7
Coupling endoplasmic reticulum stress to the cell death program: role of the ER chaperone GRP78.
FEBS Lett. 2002 Mar 13;514(2-3):122-8. doi: 10.1016/s0014-5793(02)02289-5.
8
Cell death: a new Par-4 the TRAIL.
Cell. 2009 Jul 23;138(2):220-2. doi: 10.1016/j.cell.2009.07.007.
10
Isthmin targets cell-surface GRP78 and triggers apoptosis via induction of mitochondrial dysfunction.
Cell Death Differ. 2014 May;21(5):797-810. doi: 10.1038/cdd.2014.3. Epub 2014 Jan 24.

引用本文的文献

2
An two-hybrid system to investigate human protein-protein interactions.
Biotechniques. 2025 Jul-Aug;77(7-8):283-295. doi: 10.1080/07366205.2025.2542028. Epub 2025 Aug 20.
3
Stress-induced translocation of the endoplasmic reticulum chaperone GRP78/BiP and its impact on human disease and therapy.
Proc Natl Acad Sci U S A. 2025 Jul 29;122(30):e2412246122. doi: 10.1073/pnas.2412246122. Epub 2025 Jul 23.
4
Endoplasmic Reticulum Stress in Cancer.
MedComm (2020). 2025 Jun 19;6(7):e70263. doi: 10.1002/mco2.70263. eCollection 2025 Jul.
5
Turn TRAIL Into Better Anticancer Therapeutic Through TRAIL Fusion Proteins.
Cancer Med. 2025 Jan;14(1):e70517. doi: 10.1002/cam4.70517.
8
A computational peptide model induces cancer cells' apoptosis by docking Kringle 5 to GRP78.
BMC Mol Cell Biol. 2023 Aug 8;24(1):25. doi: 10.1186/s12860-023-00484-3.
9
Aberrant LYZ expression in tumor cells serves as the potential biomarker and target for HCC and promotes tumor progression via csGRP78.
Proc Natl Acad Sci U S A. 2023 Jul 18;120(29):e2215744120. doi: 10.1073/pnas.2215744120. Epub 2023 Jul 10.

本文引用的文献

1
Vorinostat and sorafenib increase ER stress, autophagy and apoptosis via ceramide-dependent CD95 and PERK activation.
Cancer Biol Ther. 2008 Oct;7(10):1648-62. doi: 10.4161/cbt.7.10.6623. Epub 2008 Oct 12.
2
Par-4 binds to topoisomerase 1 and attenuates its DNA relaxation activity.
Cancer Res. 2008 Aug 1;68(15):6190-8. doi: 10.1158/0008-5472.CAN-08-0831.
3
Cancer resistance in transgenic mice expressing the SAC module of Par-4.
Cancer Res. 2007 Oct 1;67(19):9276-85. doi: 10.1158/0008-5472.CAN-07-2124.
4
GRP78 induction in cancer: therapeutic and prognostic implications.
Cancer Res. 2007 Apr 15;67(8):3496-9. doi: 10.1158/0008-5472.CAN-07-0325.
5
Inactivation of the candidate tumor suppressor par-4 in endometrial cancer.
Cancer Res. 2007 Mar 1;67(5):1927-34. doi: 10.1158/0008-5472.CAN-06-2687.
7
Expression of stress response protein Grp78 is associated with the development of castration-resistant prostate cancer.
Clin Cancer Res. 2006 Oct 15;12(20 Pt 1):5987-93. doi: 10.1158/1078-0432.CCR-06-0133.
8
Endoplasmic reticulum stress induction of insulin-like growth factor-binding protein-1 involves ATF4.
J Biol Chem. 2006 Jul 14;281(28):19124-33. doi: 10.1074/jbc.M602157200. Epub 2006 May 10.
10
Binding and phosphorylation of par-4 by akt is essential for cancer cell survival.
Mol Cell. 2005 Oct 7;20(1):33-44. doi: 10.1016/j.molcel.2005.08.016.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验