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Nur77的相分离通过促进Nur77/Bcl-2凝聚物的形成介导XS561诱导的细胞凋亡。

Phase separation of Nur77 mediates XS561-induced apoptosis by promoting the formation of Nur77/Bcl-2 condensates.

作者信息

Chen Xiaohui, Gao Meichun, Xia Yongzhen, Wang Xin, Qin Jingbo, He Hongying, Liu Weirong, Zhang Xiaowei, Peng Shuangzhou, Zeng Zhiping, Su Ying, Zhang Xiaokun

机构信息

School of Pharmaceutical Science, Fujian Provincial Key Laboratory of Innovative Drug Target Research, Xiamen University, Xiamen 361002, China.

Department of Clinical Laboratory, the Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai 519000, China.

出版信息

Acta Pharm Sin B. 2024 Mar;14(3):1204-1221. doi: 10.1016/j.apsb.2023.11.017. Epub 2023 Nov 17.

Abstract

The orphan nuclear receptor Nur77 is a critical regulator of the survival and death of tumor cells. The pro-death effect of Nur77 can be regulated by its interaction with Bcl-2, resulting in conversion of Bcl-2 from a survival to killer. As Bcl-2 is overexpressed in various cancers preventing them from apoptosis and promoting their resistance to chemotherapy, targeting the apoptotic pathway of Nur77/Bcl-2 may lead to new cancer therapeutics. Here, we report our identification of XS561 as a novel Nur77 ligand that induces apoptosis of tumor cells by activating the Nur77/Bcl-2 pathway. and animal studies revealed an apoptotic effect of XS561 in a range of tumor cell lines including MDA-MB-231 triple-negative breast cancer (TNBC) and MCF-7/LCC2 tamoxifen-resistant breast cancer (TAMR) in a Nur77-dependent manner. Mechanistic studies showed XS561 potently induced the translocation of Nur77 from the nucleus to mitochondria, resulting in mitochondria-related apoptosis. Interestingly, XS561-induced accumulation of Nur77 at mitochondria was associated with XS561 induction of Nur77 phase separation and the formation of Nur77/Bcl-2 condensates. Together, our studies identify XS561 as a new activator of the Nur77/Bcl-2 apoptotic pathway and reveal a role of phase separation in mediating the apoptotic effect of Nur77 at mitochondria.

摘要

孤儿核受体Nur77是肿瘤细胞存活和死亡的关键调节因子。Nur77的促死亡作用可通过其与Bcl-2的相互作用来调节,导致Bcl-2从存活因子转变为杀手因子。由于Bcl-2在多种癌症中过度表达,阻止细胞凋亡并促进其对化疗的抗性,靶向Nur77/Bcl-2的凋亡途径可能会带来新的癌症治疗方法。在此,我们报告我们鉴定出XS561是一种新型的Nur77配体,它通过激活Nur77/Bcl-2途径诱导肿瘤细胞凋亡。动物研究显示,XS561在一系列肿瘤细胞系中具有凋亡作用,包括MDA-MB-231三阴性乳腺癌(TNBC)和MCF-7/LCC2耐他莫昔芬乳腺癌(TAMR),且呈Nur77依赖性。机制研究表明,XS561能有效诱导Nur77从细胞核转位至线粒体,从而导致与线粒体相关的凋亡。有趣的是,XS561诱导的Nur77在线粒体上的积累与XS561诱导的Nur77相分离以及Nur77/Bcl-2凝聚物的形成有关。总之,我们的研究确定XS561是Nur77/Bcl-2凋亡途径的新激活剂,并揭示了相分离在介导Nur77在线粒体上的凋亡作用中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488d/10935061/211d8710bdca/ga1.jpg

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