Abstract P22: Progestin (R5020) Induced Cell Apoptosis Via Mitochondria-Mediated Cell Death Pathway In MCF-7 Cell With PRB Overexpression

IF 16.6 1区 医学 Q1 ONCOLOGY
Qian Yee Woo, Pheck Khee Lau, Meng Wei, Shi Hao Lee, Kye Siong Leong, Natasa Bajalovic, Valerie C.L Lin
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引用次数: 0

Abstract

Progestin has been widely reported to exert growth stimulatory or inhibitory effects on breast cancer cells depending on the cellular context. Our previous research showed that Promegestone (R5020) treatment induced apoptosis in MCF-7 cells with overexpression of PRB (MCF-7PRB), which paradoxically associated with massive downregulation of the known pro-apoptotic protein such as PARP, BID, Caspase 7 and 8. The objective of this study was to find out the mechanism of R5020-induced apoptosis in MCF-7PRB cells. Proteomic profiling of total cell lysates of control and R5020 treated MCF-7PRB cells were conducted using Tandem Mass Tag (TMT). HYPOXIA was found to be the topmost enriched Hallmark in R5020 treated cells. Western blotting analysis confirmed that HIF1A, BNIP3, and BNIP3L/NIX were massively upregulated in R5020 treated cells. BNIP3 and BNIP3L/NIX, the downstream apoptosis mediator of HIF1A can cause mitochondria dysfunction by forming pores on the mitochondria outer membrane or interacting with BCL-2 or BCL-xL. Indeed, mitotracker staining showed fragmented mitochondria, and this is associated with increased cytochrome C leakage into the cytoplasm and increased level of pro- and cleaved caspase 9 in R5020 treated cells. Furthermore, R5020 induced marked increases in many mitochondrial proteins including Apoptosis-Inducing Factor (AIF/AIFM1), AIFM2, Endonuclease G (EndoG), High Temperature Requirement A2 (HTRA2/ OMI), Second Mitochondria-Derived Activator of Caspases (Smac/DIABLO) and PARL (Presenilin-associated rhomboid-like), endonuclease G and Htra2/Omi, all of which are proapoptotic. For example, AIF/AIFM1and AIFM2 have been shown to induce caspase independent apoptosis by recruiting DNA nuclease such as ENGOG to the nuclease and causing chromatin condensation and DNA fragmentation. In conclusion, progestin induces mitochondria mediated apoptosis in breast cancer cells by activation of hypoxia pathway, upregulation of many proapoptotic mitochondrial proteins and downregulation of anti-apoptotic proteins BCL-2 and BCL-XL. Citation Format: Qian Yee Woo, Pheck Khee Lau, Meng Wei, Shi Hao Lee, Kye Siong Leong, Natasa Bajalovic, Valerie C.L Lin. Progestin (R5020) Induced Cell Apoptosis Via Mitochondria-Mediated Cell Death Pathway In MCF-7 Cell With PRB Overexpression [abstract]. In: Proceedings of Frontiers in Cancer Science 2024; 2024 Nov 13-15; Singapore. Philadelphia (PA): AACR; Cancer Res 2025;85(15_Suppl): nr P22.
P22:黄体酮(R5020)通过线粒体介导的细胞死亡途径诱导PRB过表达MCF-7细胞凋亡
黄体酮已被广泛报道对乳腺癌细胞发挥生长刺激或抑制作用,这取决于细胞环境。我们之前的研究表明,Promegestone (R5020)处理诱导MCF-7细胞凋亡,PRB (MCF-7PRB)过表达,这与已知的促凋亡蛋白如PARP、BID、Caspase 7和8的大量下调相矛盾。本研究旨在探讨r5020诱导MCF-7PRB细胞凋亡的机制。使用串联质量标记(Tandem Mass Tag, TMT)对对照和R5020处理的MCF-7PRB细胞的总细胞裂解物进行蛋白质组学分析。在R5020处理的细胞中,缺氧是最显著的特征。Western blotting分析证实,在R5020处理的细胞中,HIF1A、BNIP3和BNIP3L/NIX大量上调。HIF1A下游凋亡介质BNIP3和BNIP3L/NIX可通过在线粒体外膜上形成孔或与BCL-2或BCL-xL相互作用导致线粒体功能障碍。事实上,有丝分裂跟踪器染色显示线粒体碎片化,这与R5020处理细胞中细胞色素C渗漏到细胞质中增加以及前和裂解caspase 9水平增加有关。此外,R5020诱导了许多线粒体蛋白的显著增加,包括凋亡诱导因子(AIF/AIFM1), AIFM2,内切酶G (EndoG),高温要求A2 (HTRA2/ OMI),第二线粒体衍生的半胱氨酸酶激活因子(Smac/DIABLO)和PARL(早老素相关的形像),内切酶G和HTRA2/ OMI,所有这些都是促凋亡。例如,AIF/ aifm1和AIFM2通过将DNA核酸酶(如ENGOG)募集到核酸酶上并引起染色质凝聚和DNA断裂,从而诱导caspase非依赖性细胞凋亡。综上所述,黄体酮通过激活缺氧通路,上调多种促凋亡线粒体蛋白,下调抗凋亡蛋白BCL-2和BCL-XL,诱导线粒体介导的乳腺癌细胞凋亡。引文格式:吴倩仪,刘菲麒,魏孟,李世豪,梁桂雄,natasha Bajalovic, Valerie C.L Lin。黄体酮(R5020)通过线粒体介导的细胞死亡途径诱导PRB过表达MCF-7细胞凋亡[摘要]。摘自:《癌症科学前沿学报》2024;2024年11月13-15日;新加坡。费城(PA): AACR;中国癌症杂志,2015;31(增刊):344 - 344。
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来源期刊
Cancer research
Cancer research 医学-肿瘤学
CiteScore
16.10
自引率
0.90%
发文量
7677
审稿时长
2.5 months
期刊介绍: Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research. With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445. Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.
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