4.4 Article

Resveratrol induces apoptosis in SGC-7901 gastric cancer cells

Journal

ONCOLOGY LETTERS
Volume 16, Issue 3, Pages 2949-2956

Publisher

SPANDIDOS PUBL LTD
DOI: 10.3892/ol.2018.9045

Keywords

resveratrol; gastric cancer; SGC-7901 cells; apoptosis; nuclear factor-B

Categories

Funding

  1. Nature Science Foundation of Hubei Province, China [2013CFB067, 2013CFB068]

Ask authors/readers for more resources

The aim of the present study was to investigate the effect of resveratrol on apoptosis in SGC-7901 gastric cancer cells and its molecular mechanisms of action. Following resveratrol treatment, the inhibition rate of SGC-7901 cells was determined using an MTT assay. The morphological changes in apoptosis were observed by fluorescence microscopy based on acridine orange/ethidium bromide double staining. Furthermore, cell cycle and apoptosis were detected using flow cytometry, and the expression levels of nuclear factor B (NF-B) as well as apoptosis-associated proteins [B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein (Bax), cleaved caspase-3 and cleaved caspase-8] were analyzed by western blotting. The results of the present study indicated that resveratrol was able to significantly inhibit the viability of SGC-7901 cells in a dose- and time-dependent manner. When treated with 200 mu M resveratrol, the inhibition rate of SGC-7901 cells reached similar to 50%. In the presence of resveratrol, the proportion of apoptotic cells was also increased in a dose-dependent manner. Flow cytometry revealed that resveratrol induced S-phase arrest of SGC-7901 cells. When treated with 50, 200 and 400 mu M resveratrol, the proportions of SGC-7901 cells in the S-phase were respectively increased to 33.8 +/- 2.42, 60.01 +/- 2.43 and 56.05 +/- 2.67%, compared with 25.62 +/- 3.29% for the control group cells in S-phase. Additionally, the levels of the pro-apoptotic proteins Bax, cleaved caspase-3 and cleaved caspase-8 were upregulated in a dose-dependent manner, whereas the level of the anti-apoptotic protein Bcl-2 was downregulated dose-dependently. Importantly, the activation of NF-B (p65) was evidently decreased following treatment with resveratrol compared with in the control group. In conclusion, the results of the present study revealed that resveratrol was able to inhibit viability and induce apoptosis in SGC-7901 cells by suppressing NF-B activation. Therefore, resveratrol may be considered as a potential drug candidate for the treatment of gastric cancer.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available