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ORIGINAL ARTICLE
Year : 2022  |  Volume : 18  |  Issue : 79  |  Page : 565-570

Apoptosis-mediated inhibition of human gastric cancer cell proliferation by cirsilineol


Department of Gastrointestinal Surgery, Second Affiliated Hospital of Naval Medical University, Shanghai, 200003, China

Correspondence Address:
Weijun Wang
Department of Gastrointestinal Surgery, Second Affiliated Hospital of Naval Medical University, No. 415 Fengyang Road, Shanghai, 200003
China
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/pm.pm_75_22

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Background: Flavonoids constitute one of the best-characterized groups of plant secondary metabolites with enormous pharmaceutical potential. A flavone type of plant flavonoid, cirsilineol, has been reported to exhibit proapoptotic effects against malignant human cells. Objectives: The present study was designed to investigate the antiproliferative effects of cirsilineol against human gastric cancer cells. Materials and Methods: Cell viability was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and colony formation assays. Apoptosis was detected by acridine orange/ethidium bromide (AO/EB) and annexin V/propidium iodide (PI) assay. Protein expression was examined by western blotting analysis. Results: The results showed cirsilineol inhibits the proliferation of human gastric cancer cells. The IC50 of cirsilineol against human gastric cancer cells (BGC-823, SGC-7901, and MGC-803) ranged from 8 to 10 μM. Nonetheless, cirsilineol exhibited comparatively lower antiproliferative effects against normal GES-1 cells. The IC50 of cirsilineol against normal GES-1 cells was found to be 120 μM. Colony formation assay showed that cirsilineol suppressed the colony formation of BGC-823 and MGC-803 cells in a dose-dependent manner. Acridine orange and ethidium bromide (AO/EB) staining showed that cirsilineol induced apoptosis in BGC-823 and MGC-803 cells. The percentage of apoptosis increased from 7.4% in control to 40.5% in BGC-823 cells and from 6.56% in control to 33.53% in MGC-803 cells at 8 μM cirsilineol. Western blotting showed cirsilineol caused an increase in Bax and cleaved caspase-3 and a decrease in Bcl-2 expression in both BGC-823 and MGC-803 cells. Conclusion: Together, the results are indicative of the proapoptotic and antitumor potential of cirsilineol against gastric cancer cells, suggestive of its possible therapeutic significance in future.


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