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A Novel Isaindigotone Derivative Displays Better Anti-Proliferation Activities and Induces Apoptosis in Gastric Cancer Cells

Kangjia DuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaCheng‐Jie YangSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaZhongkun ZhouSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaYunhao MaSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaYanan TianSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaRentao ZhangSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaHao ZhangSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaXinrong JiangSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaHongmei ZhuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaHuanxiang LiuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaPeng ChenSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, ChinaYing‐Qian LiuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730020, China
2022en
ABI

Аннотация

Isaindigotone is an alkaloid containing a pyrrolo-[2,1-b]quinazoline moiety conjugated with a benzylidene group and isolated from the root of Isatis indigotca Fort. However, further anticancer activities of this alkaloid and its derivatives have not been fully explored. In this work, a novel isaindigotone derivative was synthesized and three different gastric cell lines and one human epithelial gastric cell line were used to study the anti-proliferation effects of the novel isaindigotone derivative BLG26. HGC27 cells and AGS cells were used to further explore the potential mechanisms. BLG26 exhibited better anti-proliferation activities in AGS cells with a half-maximal inhibitory concentration (IC50) of 1.45 μM. BLG26 caused mitochondrial membrane potential loss and induced apoptosis in both HGC27 cells and AGS cells by suppressing mitochondrial apoptotic pathway and PI3K/AKT/mTOR axis. Acute toxicity experiment showed that LD50 (median lethal dose) of BLG26 was above 1000.0 mg/kg. This research suggested that BLG26 can be a potential candidate for the treatment of gastric cancer.

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