Design, Synthesis and Biological Evaluation of Novel MDH Inhibitors Targeting Tumor Microenvironment

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초록

MDH1 and MDH2 enzymes play an important role in the survival of lung cancer. In this study, a novel series of dual MDH1/2 inhibitors for lung cancer was rationally designed and synthesized, and their SAR was carefully investigated. Among the tested compounds, compound 50 containing a piperidine ring displayed an improved growth inhibition of A549 and H460 lung cancer cell lines compared with LW1497. Compound 50 reduced the total ATP content in A549 cells in a dose-dependent manner; it also significantly suppressed the accumulation of hypoxia-inducible factor 1-alpha (HIF-1a) and the expression of HIF-1a target genes such as GLUT1 and pyruvate dehydrogenase kinase 1 (PDK1) in a dose-dependent manner. Furthermore, compound 50 inhibited HIF-1a-regulated CD73 expression under hypoxia in A549 lung cancer cells. Collectively, these results indicate that compound 50 may pave the way for the development of next-generation dual MDH1/2 inhibitors to target lung cancer.

키워드

MDH1/2; inhibitors; HIF-1 alpha; lung cancer; NICOTINAMIDE ADENINE-DINUCLEOTIDE; MALATE-ASPARTATE SHUTTLE; DEHYDROGENASE; CANCER; GLUCOSE; ADAPTATION; HALLMARKS; GLUTAMINE; HYPOXIA; CELLS
제목
Design, Synthesis and Biological Evaluation of Novel MDH Inhibitors Targeting Tumor Microenvironment
저자
Godesi, Sreenivasulu; Han, Jeong-Ran; Kim, Jang-Keun; Kwak, Dong-Ik; Lee, Joohan; Nada, Hossam; Kim, Minkyoung; Yang, Hyun-A; Im, Joo-Young; Ban, Hyun Seung; Lee, Chang Hoon; Choi, Yongseok; Won, Misun; Lee, Kyeong
DOI
10.3390/ph16050683
발행일
2023-05
유형
Article
저널명
Pharmaceuticals
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16
호
5
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