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Article Publish Status: FREE
Abstract Title:

Methylsulfonylmethane inhibits HER2 expression through STAT5b in breast cancer cells.

Abstract Source:

Int J Oncol. 2016 Feb ;48(2):836-42. Epub 2015 Dec 7. PMID: 26648017

Abstract Author(s):

Dong Young Kang, Pramod Darvin, Young Beom Yoo, Youn Hee Joung, Nipin Sp, Hyo Joo Byun, Young Mok Yang

Article Affiliation:

Dong Young Kang

Abstract:

Breast cancer is the most common cancer in women globally. The factors that increase risk include: late age atfirst birth, alcohol, radiation exposure, family history of breast cancer, and postmenopausal hormone therapy. Numerous drugs are being developed to treat breast cancer. Among them, Herceptin is used for the treatment of human epidermal growth factor receptor 2 (HER2)-positive cases and targets HER2 effectively and efficiently, but it is very expensive. Methylsulfonylmethane (MSM) is an organic sulfur-containing natural compound having no reported toxicity. We examined MSM in breast cancer cell lines and found it inhibited the proliferation of estrogen receptor-positive and HER2-positive breast cancer cells in a dose-dependent manner. It also suppressed the activation of STAT5b and expression of HER2 in breast cancer cells. We determined the STAT5b binding site (GAS element) in the HER2 gene. Detailed analysis showed that MSM decreased the ability of STAT5b to bind the promoter of the HER2 gene and a luciferase assay demonstrated reduced activity. We confirmed that MSM can effectively regulate STAT5b, and thereby decrease HER2 expression. Therefore, we recommend the use of MSM as an inhibitor for the management of HER2-positive breast cancers.

Study Type : In Vitro Study

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Sayer Ji
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