Hanada Eiki, Kageyama Susumu, Murai Ryosuke, Kubota Shigehisa, Ii Hiromi, Nakata Susumu, Kita Hiroko, Kawauchi Akihiro, Chano Tokuhiro
Department of Urology, Shiga University of Medical Science, Shiga, Japan.
Department of Urology, Shiga University of Medical Science, Shiga, Japan
Anticancer Res. 2019 Apr;39(4):1893-1898. doi: 10.21873/anticanres.13297.
BACKGROUND/AIM: γ-Glutamylcyclotransferase (GGCT), a key enzyme involved in glutathione metabolism, catalyzes a specific reaction that generates 5-oxoproline and free amino acids from the γ-glutamyl peptide. Inhibition of GGCT is a promising therapeutic strategy for the treatment of various cancers.
Immuno-histochemistry was used to evaluate GGCT expression in bladder tumors. The growth inhibitory effect of pro-GA, a novel GGCT inhibitor, in the presence or absence of mitomycin C (MMC) was assessed in three distinct bladder cancer cell lines.
Over half of the clinical bladder tumor samples overexpressed GGCT. Pro-GA reduced the growth of all bladder cancer cell lines in a dose-dependent manner, and increased the anti-tumor effect of MMC.
Inhibition of GGCT using pro-GA provides a novel therapeutic strategy for the treatment of bladder cancers.
背景/目的:γ-谷氨酰环转移酶(GGCT)是参与谷胱甘肽代谢的关键酶,催化从γ-谷氨酰肽生成5-氧代脯氨酸和游离氨基酸的特定反应。抑制GGCT是治疗多种癌症的一种有前景的治疗策略。
采用免疫组织化学法评估GGCT在膀胱肿瘤中的表达。在三种不同的膀胱癌细胞系中评估新型GGCT抑制剂原GA在有或无丝裂霉素C(MMC)存在时的生长抑制作用。
超过一半的临床膀胱肿瘤样本中GGCT过表达。原GA以剂量依赖的方式降低了所有膀胱癌细胞系的生长,并增强了MMC的抗肿瘤作用。
使用原GA抑制GGCT为膀胱癌的治疗提供了一种新的治疗策略。