期刊
ARABIAN JOURNAL OF CHEMISTRY
卷 15, 期 3, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.arabjc.2021.103644
关键词
1,2,4-Triazine; Chalcone; Antiproliferative activity; ROS; ERK; DR5
资金
- National Natural Sciences Foundations of China [U2004123]
- Henan Association of Science and Technology (China) [2020HYTP056]
- Science and Technology Department of Henan Province (China) [20202310144]
- open fund of state key laboratory of Pharmaceutical Biotechnology, Nanjing University, China [KF-GN-202101]
In this study, novel 1,2,4-triazine-chalcone hybrids were designed and synthesized, with compound 9l showing significant antiproliferative activity against various cancer cell lines via the ROS-ERK-DR5 axis. Compound 9l effectively inhibited gastric cancer cell growth in vitro and in vivo, making it a promising anti-gastric cancer agent.
In this work, a series of novel 1,2,4-triazine-chalcone hybrids were designed through the molecular hybridization strategy, synthesized by two step chlorinations and further aldol condensation and evaluated their antiproliferative activity against MGC-803, HCT-116, PC-3, EC-109 and A549 cells. Compound 9l displayed significant antiproliferative activity against MGC-803, HCT-116, PC-3, EC-109 and A549 cell lines with IC50 values of 0.41, 0.43, 0.61, 0.78 and 0.52 mu M, respectively. Subsequent mechanistic investigations suggested that compound 9l induced the generation of ROS and inhibited the activation of the ERK pathway. Compound 9l induced extrinsic cell apoptosis by up-regulating DR5 dependent on the generation of ROS, while upregulation of DR5 caused by compound 9l relied on the inhibition of ERK. Thus, compound 9l inhibited the gastric cancer cells via an axis of ROS-ERK-DR5 in vitro. Compound 9l also showed potent activity on cell proliferation inhibition, and was effective in suppressing the growth of MGC-803 xenograft tumor in nude mice without obvious toxicity. Therefore, compound 9l is to be reported as anti-gastric cancer agent in vitro and in vivo via an axis of ROS-ERK-DR5. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.
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