Suppr超能文献

鞣花酸通过调节结直肠癌中的膜联蛋白 A1 调控细胞凋亡-自噬转换。

Punicalagin Regulates Apoptosis-Autophagy Switch via Modulation of Annexin A1 in Colorectal Cancer.

机构信息

Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia.

出版信息

Nutrients. 2020 Aug 13;12(8):2430. doi: 10.3390/nu12082430.

Abstract

Punicalagin (PU), a polyphenol extracted from pomegranate () husk is proven to have anti-cancer effects on different types of cancer including colorectal cancer (CRC). Its role in modulating endogenous protein as a means of eliciting its anti-cancer effects, however, has not been explored to date. Hence, this study aimed to investigate the role of PU in modulating the interplay between apoptosis and autophagy by regulating Annexin A1 (Anx-A1) expression in HCT 116 colorectal adenocarcinoma cells. In the study, selective cytotoxicity, pro-apoptotic, autophagic and Anx-A1 downregulating properties of PU were shown which indicate therapeutic potential that this polyphenol has against CRC. Autophagy flux analysis via flow cytometry showed significant autophagosomes degradation in treated cells, proving the involvement of autophagy. Proteome profiling of 35 different proteins in the presence and absence of Anx-A1 antagonists in PU-treated cells demonstrated a complex interplay that happens between apoptosis and autophagy that suggests the possible simultaneous induction and inhibition of these two cell death mechanisms by PU. Overall, this study suggests that PU induces autophagy while maintaining basal level of apoptosis as the main mechanisms of cytotoxicity via the modulation of Anx-A1 expression in HCT 116 cells, and thus has a promising translational potential.

摘要

鞣花酸(PU)是从石榴皮中提取的多酚,已被证明对包括结直肠癌(CRC)在内的多种癌症具有抗癌作用。然而,迄今为止,其作为一种调节内源性蛋白质从而发挥抗癌作用的方式尚未得到探索。因此,本研究旨在通过调节 HCT 116 结直肠腺癌细胞中 Annexin A1(Anx-A1)的表达,研究 PU 在调节细胞凋亡和自噬相互作用中的作用。在研究中,显示了 PU 的选择性细胞毒性、促凋亡、自噬和 Anx-A1 下调特性,表明这种多酚对 CRC 具有治疗潜力。通过流式细胞术进行的自噬通量分析显示,处理后的细胞中自噬体明显降解,证明自噬的参与。在存在和不存在 Anx-A1 拮抗剂的情况下,对 PU 处理细胞中的 35 种不同蛋白质进行蛋白质组分析,表明细胞凋亡和自噬之间发生了复杂的相互作用,这表明 PU 可能同时诱导和抑制这两种细胞死亡机制。总的来说,这项研究表明,PU 通过调节 HCT 116 细胞中 Anx-A1 的表达,诱导自噬,同时保持细胞凋亡的基础水平,作为细胞毒性的主要机制,因此具有有希望的转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366e/7468705/96486e8fb598/nutrients-12-02430-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验