Feng Qi, Li Xiuru, Sun Wenjing, Li Yubo, Yuan Yu, Guan Baozhang, Zhang Shuai
The First Affiliated Hospital, Biomedical Translational Research Institute, Jinan University, Guangzhou, Guangdong 510632, People's Republic of China.
Tianjin State Key Laboratory of Modern Chinese Medicine, School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, People's Republic of China.
Cancer Manag Res. 2020 Aug 5;12:6921-6934. doi: 10.2147/CMAR.S254853. eCollection 2020.
The 6-phosphogluconate dehydrogenase (6PGD) was upregulated in many solid cancers and plays an important role in tumorigenesis. In the present study, we want to discover an old drug as an inhibitor of 6PGD for suppressing tumor growth.
We determined the expression of 6PGD in cancer tissues using Gene Expression Omnibus (GEO) profiles and explored the importance of 6PGD expression in cancer progression by using Kaplan-Meier Plotter. We identified Ebselen as a 6PGD inhibitor by using 6PGD in vitro enzyme activity assay. Cell viability, cell proliferation, tumor growth and cell metabolism assay were used to explore the role of 6PGD and its inhibitor in cancer cells.
We found that the expression of 6PGD was upregulated in different cancer tissues and it can promote tumorigenesis. Here, we analyzed our 6PGD inhibitor screening data again and found an old drug Ebselen, which blocks cancer cell proliferation and tumor growth by inhibiting 6PGD enzyme activity, while knocking down 6PGD would partially abolish the inhibition of Ebselen on cell proliferation and cell metabolism.
Our results suggested that the conventional drug Ebselen could serve as a novel inhibitor of 6PGD for suppressing cancer growth by inhibiting 6PGD enzyme activity.
6-磷酸葡萄糖酸脱氢酶(6PGD)在多种实体癌中表达上调,在肿瘤发生过程中发挥重要作用。在本研究中,我们希望找到一种旧药作为6PGD的抑制剂来抑制肿瘤生长。
我们使用基因表达综合数据库(GEO)分析癌症组织中6PGD的表达,并通过Kaplan-Meier Plotter探索6PGD表达在癌症进展中的重要性。我们通过6PGD体外酶活性测定确定依布硒仑为6PGD抑制剂。采用细胞活力、细胞增殖、肿瘤生长和细胞代谢测定来探索6PGD及其抑制剂在癌细胞中的作用。
我们发现6PGD在不同癌症组织中表达上调,且能促进肿瘤发生。在此,我们再次分析6PGD抑制剂筛选数据,发现一种旧药依布硒仑,它通过抑制6PGD酶活性来阻断癌细胞增殖和肿瘤生长,而敲低6PGD会部分消除依布硒仑对细胞增殖和细胞代谢的抑制作用。
我们的结果表明,传统药物依布硒仑可作为一种新型6PGD抑制剂,通过抑制6PGD酶活性来抑制癌症生长。