Journal of Medicinal Chemistry
Journal of Medicinal Chemistry
5 years ago

Synthesis of Potent and Selective Inhibitors of Aldo-Keto Reductase 1B10 and Their Efficacy against Proliferation, Metastasis, and Cisplatin Resistance of Lung Cancer Cells

Synthesis of Potent and Selective Inhibitors of Aldo-Keto Reductase 1B10 and Their Efficacy against Proliferation, Metastasis, and Cisplatin Resistance of Lung Cancer Cells
Satoshi Endo, Miho Suyama, Shuang Xia, Yoshinori Ao, Akira Ikari, Yoshikazu Horino, Kazuo Kuwata, Akira Hara, Toshiyuki Matsunaga, Dawei Hu, Satoyuki Takahara, Yoshihiro Hayakawa, Hiroaki Gouda, Hiroaki Oguri, Yurie Watanabe, Naoki Toyooka, Yoshifumi Morikawa
Aldo-keto reductase 1B10 (AKR1B10) is overexpressed in several extraintestinal cancers, particularly in non-small-cell lung cancer, where AKR1B10 is a potential diagnostic marker and therapeutic target. Selective AKR1B10 inhibitors are required because compounds should not inhibit the highly related aldose reductase that is involved in monosaccharide and prostaglandin metabolism. Currently, 7-hydroxy-2-(4-methoxyphenylimino)-2H-chromene-3-carboxylic acid benzylamide (HMPC) is known to be the most potent competitive inhibitor of AKR1B10, but it is nonselective. In this study, derivatives of HMPC were synthesized by removing the 4-methoxyphenylimino moiety and replacing the benzylamide with phenylpropylamide. Among them, 4c and 4e showed higher AKR1B10 inhibitory potency (IC50 4.2 and 3.5 nM, respectively) and selectivity than HMPC. The treatments with the two compounds significantly suppressed not only migration, proliferation, and metastasis of lung cancer A549 cells but also metastatic and invasive potentials of cisplatin-resistant A549 cells.

Publisher URL: http://dx.doi.org/10.1021/acs.jmedchem.7b00830

DOI: 10.1021/acs.jmedchem.7b00830

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