Suppr超能文献

探讨从眼镜蛇毒液中提取的细胞毒素 10 的抗癌潜力:来自乳腺癌和肺癌细胞系的机制见解。

Exploring the anticancer potential of Cytotoxin 10 from Naja kaouthia venom: Mechanistic insights from breast and lung cancer cell lines.

机构信息

Department of Molecular Biology and Biotechnology, School of Sciences, Tezpur University, Assam, 784028, India.

Department of Molecular Biology and Biotechnology, School of Sciences, Tezpur University, Assam, 784028, India.

出版信息

Chem Biol Interact. 2024 Nov 1;403:111254. doi: 10.1016/j.cbi.2024.111254. Epub 2024 Sep 24.

Abstract

Breast and lung cancers are the leading causes of cancer-related deaths in the world. Although considerable progress has been made in the field of cancer therapy, quest to discover potent, safe and cost-effective alternatives especially from natural sources is being pursued. Snake venom, which is a treasure trove of various peptides and proteins including natural toxins that specifically target tissues and receptors in the envenomated victims. Many such proteins are being explored for their therapeutic potential against various diseases including cancers. Here, we report the mechanism of cytotoxic activity of crude venom and a purified protein, Cytotoxin from the monocled cobra (Naja kaouthia), an elapid snake with neurotoxic venom prominently found in the North-East India. The crude venom showed significant cytotoxicity against breast (MCF-7and MDA-MB-231) and lung (A549, NCI-H522) cancer cell lines. Bioassay-guided fractionation using RP-HPLC showed highest cytotoxic activity in peak P9. Liquid chromatography-tandem mass spectrometry (ESI-LC-MS/MS) analysis was employed and the fraction is identified as Cytotoxin 10 which showed comparable cytotoxicity against the experimental cell lines. Cytotoxin 10 also exhibited apoptosis in MCF-7 and A549 cell lines using AO/EtBr and flow cytometry analysis. Expressions of apoptosis related proteins e.g. Bax, Bcl-2, Caspase-7 and PARP were also studied following Cytotoxin 10 treatment in both cell lines. Molecular docking experiments performed to investigate the interactions between Cytotoxin 10 and the apoptotic proteins revealed favourable binding scores compared to their corresponding inhibitors. Interestingly, Cytotoxin 10 inhibited migration and adhesion in a time and dose-dependent manner in both MCF-7 and A549 cells. This is the first report elucidating the mechanism of cytotoxic activity of Cytotoxin 10 purified from Naja kaouthia venom of North-East India origin and could pave the way for development of potential therapeutic strategies against breast and lung cancer.

摘要

乳腺癌和肺癌是全球癌症相关死亡的主要原因。尽管在癌症治疗领域取得了相当大的进展,但人们仍在探索从天然来源寻找有效、安全且具有成本效益的替代物,特别是从蛇毒中寻找。蛇毒是各种肽和蛋白质的宝库,包括专门针对中毒受害者组织和受体的天然毒素。许多此类蛋白质正在被探索用于治疗各种疾病,包括癌症。在这里,我们报告了来自单眼眼镜蛇(Naja kaouthia)的粗毒液和一种纯化蛋白细胞毒素的细胞毒性作用机制,单眼眼镜蛇是一种具有神经毒性毒液的眼镜蛇,在印度东北部广泛存在。粗毒液对乳腺癌(MCF-7 和 MDA-MB-231)和肺癌(A549、NCI-H522)癌细胞系表现出显著的细胞毒性。使用 RP-HPLC 进行的生物测定指导的馏分分离显示,在 P9 峰中显示出最高的细胞毒性活性。采用液相色谱-串联质谱(ESI-LC-MS/MS)分析,该馏分被鉴定为细胞毒素 10,对实验细胞系表现出相当的细胞毒性。细胞毒素 10 还在 MCF-7 和 A549 细胞系中通过 AO/EtBr 和流式细胞术分析显示出凋亡。在用细胞毒素 10 处理这两种细胞系后,还研究了凋亡相关蛋白(如 Bax、Bcl-2、Caspase-7 和 PARP)的表达。进行分子对接实验以研究细胞毒素 10 与凋亡蛋白之间的相互作用,结果显示与相应抑制剂相比具有有利的结合评分。有趣的是,细胞毒素 10 以时间和剂量依赖性方式抑制 MCF-7 和 A549 细胞的迁移和粘附。这是首次阐明从印度东北部来源的单眼眼镜蛇毒液中纯化的细胞毒素 10 的细胞毒性作用机制的报告,为开发针对乳腺癌和肺癌的潜在治疗策略铺平了道路。

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