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线粒体PAK6通过PAK6-SIRT4-ANT2复合物抑制前列腺癌细胞凋亡。

Mitochondrial PAK6 inhibits prostate cancer cell apoptosis the PAK6-SIRT4-ANT2 complex.

作者信息

Li Tingting, Li Yang, Liu Tong, Hu Bingtao, Li Jiabin, Liu Chen, Liu Tao, Li Feng

机构信息

Department of Cell Biology, Key Laboratory of Cell Biology, National Health Commission of the PRC, and Key Laboratory of Medical Cell Biology, Ministry of Education of the PRC, Shenyang 110122, Liaoning, China.

Medical Research Center, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing 100191, China.

出版信息

Theranostics. 2020 Feb 3;10(6):2571-2586. doi: 10.7150/thno.42874. eCollection 2020.

Abstract

: P21-activated kinase 6 (PAK6) is a member of the class II PAKs family, which is a conserved family of serine/threonine kinases. Although the effects of PAK6 on many malignancies, especially in prostate cancer, have been studied for a long time, the role of PAK6 in mitochondria remains unknown. : The expression of PAK6, SIRT4 and ANT2 in prostate cancer and adjacent non-tumor tissues was detected by immunohistochemistry. Immunofuorescence and immunoelectron microscopy were used to determine the subcellular localization of PAK6. Immunoprecipitation, immunofuorescence and ubiquitination assays were performed to determine how PAK6 regulates SIRT4, how SIRT4 regulates ANT2, and how PAK6 regulates ANT2. Flow cytometry detection and xenograft models were used to evaluate the impact of ANT2 mutant expression on the prostate cancer cell cycle and apoptosis regulation. : The present study revealed that the PAK6-SIRT4-ANT2 complex is involved in mitochondrial apoptosis in prostate cancer cells. It was found that PAK6 is mainly located in the mitochondrial inner membrane, in which PAK6 promotes SIRT4 ubiquitin-mediated proteolysis. Furthermore, SIRT4 deprives the ANT2 acetylation at K105 to promote its ubiquitination degradation. Hence, PAK6 adjusts the acetylation level of ANT2 through the PAK6-SIRT4-ANT2 pathway, in order to regulate the stability of ANT2. Meanwhile, PAK6 directly phosphorylates ANT2 atT107 to inhibit the apoptosis of prostate cancer cells. Therefore, the phosphorylation and deacetylation modifications of ANT2 are mutually regulated, leading to tumor growth . Consistently, these clinical prostate cancer tissue evaluations reveal that PAK6 is positively correlated with ANT2 expression, but negatively correlated with SIRT4. : These present findings suggest the pivotal role of the PAK6-SIRT4-ANT2 complex in the apoptosis of prostate cancer. This complex could be a potential biomarker for the treatment and prognosis of prostate cancer.

摘要

p21激活激酶6(PAK6)是II类PAK家族的成员,该家族是丝氨酸/苏氨酸激酶的保守家族。尽管PAK6对许多恶性肿瘤,尤其是前列腺癌的影响已被研究了很长时间,但PAK6在线粒体中的作用仍然未知。

通过免疫组织化学检测PAK6、SIRT4和ANT2在前列腺癌及相邻非肿瘤组织中的表达。采用免疫荧光和免疫电子显微镜确定PAK6的亚细胞定位。进行免疫沉淀、免疫荧光和泛素化分析,以确定PAK6如何调节SIRT4、SIRT4如何调节ANT2以及PAK6如何调节ANT2。使用流式细胞术检测和异种移植模型评估ANT2突变体表达对前列腺癌细胞周期和凋亡调控的影响。

本研究表明,PAK6-SIRT4-ANT2复合物参与前列腺癌细胞的线粒体凋亡。发现PAK6主要位于线粒体内膜,其中PAK6促进SIRT4泛素介导的蛋白水解。此外,SIRT4剥夺ANT2在K105处的乙酰化以促进其泛素化降解。因此,PAK6通过PAK6-SIRT4-ANT2途径调节ANT2的乙酰化水平,以调节ANT2的稳定性。同时,PAK6直接在T107处磷酸化ANT2以抑制前列腺癌细胞的凋亡。因此,ANT2的磷酸化和去乙酰化修饰相互调节,导致肿瘤生长。一致地,这些临床前列腺癌组织评估显示,PAK6与ANT2表达呈正相关,但与SIRT4呈负相关。

这些研究结果表明PAK6-SIRT4-ANT2复合物在前列腺癌凋亡中起关键作用。该复合物可能是前列腺癌治疗和预后的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de24/7052886/a992a9ca55b3/thnov10p2571g001.jpg

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