Manea Marilena, Mező Gábor
Research Group of Peptide Chemistry, Hungarian Academy of Sciences, Eotvos L. University, 1117 Budapest, Pazmany P. stny. 1/A, Hungary.
Protein Pept Lett. 2013 Apr;20(4):439-49.
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.
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。