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Abstract Title:

Methylsulfonylmethane Induces GArrest and Mitochondrial Apoptosis in YD-38 Gingival Cancer Cells.

Abstract Source:

Anticancer Res. 2017 04 ;37(4):1637-1646. PMID: 28373424

Abstract Author(s):

Nipin S P, Dong Young Kang, Baek Joong Kim, Youn Hee Joung, Pramod Darvin, Hyo Joo Byun, Joong Gon Kim, Je Uk Park, Young Mok Yang

Article Affiliation:

Nipin S P

Abstract:

Gingival squamous cell carcinoma is a rare form of cancer that accounts for less than 10% of all head and neck cancers. Targeted therapies with natural compounds are of interest because they possess high efficacy with fewer side-effects. Methylsulfonylmethane (MSM) is an organic sulfur-containing compound with anticancer activities. The main goal of this study was to induce proliferation inhibition and apoptosis in the metastatic YD-38 cell line. MSM up-regulated expression of P21and P27genes and down-regulated expression of cyclin D1 (CCND1) and CDK4. Moreover, treatment with MSM induced apoptosis and up-regulation of BAX in YD-38 cells. In accordance, the expression of the BCL-2 and BCL-XL, were inhibited, indicating the role of mitochondria in MSM-induced apoptosis. Analysis of mitochondrial integrity showed a loss of mitochondrial potential with an increased level of cytochrome c in the cytosol compared to mitochondria. Active CASPASE-3 (CASP3) was also observed, confirming that MSM-induced apoptosis is caspase-mediated.

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Sayer Ji
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