Suppr超能文献

促性腺激素释放激素III——抗癌药物开发的一个有前景的候选物。

lGnRH-III -- a promising candidate for anticancer drug development.

作者信息

Manea Marilena, Mező Gábor

机构信息

Research Group of Peptide Chemistry, Hungarian Academy of Sciences, Eotvos L. University, 1117 Budapest, Pazmany P. stny. 1/A, Hungary.

出版信息

Protein Pept Lett. 2013 Apr;20(4):439-49.

Abstract

Lamprey gonadotropin-releasing hormone-III (lGnRH-III; Glp-His-Trp-Ser-His-Asp-Trp-Lys-Pro-Gly-NH2), a native isoform of human GnRH (GnRH-I), was initially isolated from the brain of the sea lamprey (Petromyzon marinus). It is a weak GnRH agonist, which exerts a direct antiproliferative effect on cancer cells and has an insignificant LH and FSH releasing potency in mammals. These features reveal the advantages of lGnRH-III and its derivatives for use in cancer therapy. Here we give an overview of various strategies to increase the antitumor activity of lGnRH-III, such as amino acid replacement, cyclization, dimerization and conjugation to polymers or to chemotherapeutic agents. In vitro and in vivo antitumor activity of lGnRH-III based compounds was demonstrated both on hormone dependent and independent tumors.

摘要

七鳃鳗促性腺激素释放激素III(lGnRH-III;Glp-His-Trp-Ser-His-Asp-Trp-Lys-Pro-Gly-NH2),人类促性腺激素释放激素(GnRH-I)的一种天然异构体,最初是从海七鳃鳗(Petromyzon marinus)的大脑中分离出来的。它是一种弱促性腺激素释放激素激动剂,对癌细胞具有直接的抗增殖作用,并且在哺乳动物中具有微不足道的促黄体生成素(LH)和促卵泡生成素(FSH)释放能力。这些特性揭示了lGnRH-III及其衍生物在癌症治疗中的优势。在此,我们概述了各种提高lGnRH-III抗肿瘤活性的策略,例如氨基酸置换、环化、二聚化以及与聚合物或化疗药物偶联。基于lGnRH-III的化合物在激素依赖性和非依赖性肿瘤上均表现出体外和体内抗肿瘤活性。

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