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撤回:茯苓酸激活TP53INP2/TRAF6/半胱天冬酶-8通路以促进肾癌细胞凋亡。

RETRACTED: Pachymic acid activates TP53INP2/TRAF6/caspase-8 pathway to promote apoptosis in renal cell carcinoma cells.

作者信息

Li Xunjia, He An, Liu Chengxuan, Li Ying, Luo Yan, Xiong Weijian, Nian Weiqi, Zuo Deyu

机构信息

Department of Nephrology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.

Department of Research and Development, Chongqing Precision Medical Industry Technology Research Institute, Chongqing, China.

出版信息

Environ Toxicol. 2025 Jul;40(7):E168-E181. doi: 10.1002/tox.24195. Epub 2024 Apr 1.

DOI:10.1002/tox.24195
PMID:38560766
Abstract

While pachymic acid (PA), a key component of Poria cocos (Schw.), has demonstrated anti-tumor effects in lung, breast, and pancreatic cancers, its impact on renal cell carcinoma (RCC) is unclear. This study evaluated the effect of PA on proliferation, migration, and apoptosis in human renal cancer A498 and ACHN cells as well as in cancer xenograft mice using wound scratch test, Western blotting, and co-immunoprecipitation assays. In a dose- and time-dependent manner, PA exhibited significant inhibition of RCC cell proliferation, migration, and invasion, accompanied by the induction of apoptosis. Additionally, PA upregulated the expression of tumor protein p53-inducible nuclear protein 2 (TP53INP2) and tumor necrosis factor receptor-associated factor 6 (TRAF6), which were downregulated in renal papillary and chromophobe carcinoma, resulting in inhibited tumor growth in mice. PA treatment elevated cleaved-caspase 3 and 8, and PARP levels, and facilitated TP53INP2 and TRAF6 binding to caspase 8, promoting its ubiquitination. Molecular docking revealed interactions between PA and TP53INP2, TRAF6. In summary, PA inhibits RCC development by upregulating TP53INP2 and promoting TRAF6-induced caspase 8 ubiquitination, activating apoptotic pathways.

摘要

虽然茯苓的关键成分茯苓酸(PA)已在肺癌、乳腺癌和胰腺癌中显示出抗肿瘤作用,但其对肾细胞癌(RCC)的影响尚不清楚。本研究使用划痕试验、蛋白质印迹法和免疫共沉淀试验,评估了PA对人肾癌A498和ACHN细胞以及癌症异种移植小鼠的增殖、迁移和凋亡的影响。PA以剂量和时间依赖性方式显著抑制RCC细胞的增殖、迁移和侵袭,并诱导细胞凋亡。此外,PA上调了肿瘤蛋白p53诱导核蛋白2(TP53INP2)和肿瘤坏死因子受体相关因子6(TRAF6)的表达,这两种蛋白在肾乳头状癌和嫌色细胞癌中表达下调,从而抑制了小鼠肿瘤的生长。PA处理提高了裂解的半胱天冬酶3和8以及PARP的水平,并促进了TP53INP2和TRAF6与半胱天冬酶8的结合,促进其泛素化。分子对接揭示了PA与TP53INP2、TRAF6之间的相互作用。总之,PA通过上调TP53INP2和促进TRAF6诱导的半胱天冬酶8泛素化,激活凋亡途径,从而抑制RCC的发展。

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