Suppr超能文献

一种特定的细胞穿透肽通过下调 Bcl-2 诱导 SKOV3 细胞凋亡。

A specific cell-penetrating peptide induces apoptosis in SKOV3 cells by down-regulation of Bcl-2.

出版信息

Biotechnol Lett. 2013 Nov;35(11):1791-7. doi: 10.1007/s10529-013-1263-x.

Abstract

Peptides are emerging as pharmaceutical agents in cancer therapy. The peptide, TLSGAFELSRDK (TLS) is a targeting ligand that can specifically triggers cellular uptake by binding to SKOV3 cells. Cell surface proteins and the C-terminal basic residues of the TLS are required for effective cell penetration, and the uptake process is energy-dependent. It inhibited the proliferation of SKOV3 cells and induced early-stage apoptosis by down-regulation of Bcl-2 expression mediated through a caspase-dependent pathway. The synergistic anti-proliferative effects of the peptide TLS and doxorubicin on SKOV3 cells were further investigated. Taken together, TLS, acting as a combination of a targeted ligand and a therapeutic agent, was a promising candidate for the development of peptide-based therapies in ovarian cancer.

摘要

肽类正在成为癌症治疗中的药物制剂。该肽 TLSGAFELSRDK(TLS)是一种靶向配体,通过与 SKOV3 细胞结合,可特异性触发细胞摄取。细胞表面蛋白和 TLS 的 C 末端碱性残基是有效穿透细胞所必需的,摄取过程是能量依赖性的。它通过 caspase 依赖性途径下调 Bcl-2 表达,抑制 SKOV3 细胞的增殖并诱导早期凋亡。进一步研究了肽 TLS 和阿霉素对 SKOV3 细胞的协同抗增殖作用。总之,TLS 作为靶向配体和治疗剂的组合,是开发卵巢癌基于肽的治疗方法的有前途的候选物。

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