4.7 Article

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

期刊

出版社

MDPI
DOI: 10.3390/ijms23148028

关键词

gastric cancer; isaindigotone; anti-proliferation; mitochondrial potential

资金

  1. Key Research and Development Program of Gansu Province [21YF5FA112]
  2. Technological Innovation Guidance Program of Gansu Province [21CX6QA127]
  3. Key Program for International S&T Cooperation Projects of China Gansu Province [18YF1WA115]
  4. National College Students' Innovation and Entrepreneurship Training Program [202210730011]
  5. College Students' Innovation and Entrepreneurship Program of Lanzhou University, China [20220260010]
  6. Innovation and Entrepreneurship Training Program of Lanzhou University, China [cxcy202207]

向作者/读者索取更多资源

A novel isaindigotone derivative BLG26 was synthesized and showed potential anti-proliferation effects in gastric cancer cells, indicating its potential as a candidate drug for gastric cancer treatment. BLG26 exhibited better activity in inhibiting tumor cell proliferation in AGS cells.
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 mu M. 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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