4.7 Article

The suppressive role of phytochemical-induced glutathione S-transferase Mu 2 in human urothelial carcinoma cells

Journal

BIOMEDICINE & PHARMACOTHERAPY
Volume 151, Issue -, Pages -

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.113102

Keywords

GlutathioneS-transferases Mu2; Tumor suppressor; SP1; DNA methylation; Berberrubine; Resveratrol

Funding

  1. Ministry of Science and Technology, Taiwan, R.O.C. [MOST108-2320-B-415-006-MY3]
  2. Dit-manson Medical Foundation Chiayi Christian Hospital, Chiayi, Taiwan [R107-002]

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Glutathione S-transferases (GSTs) play an important role in metabolism and detoxification of various substances. A study found that GSTM2 gene expression is lower in advanced stages of bladder urothelial carcinoma, and overexpression of GSTM2 inhibits invasion, migration, and tumor formation of bladder cancer cells. The study also identified an SP1 site and several phytochemicals that can affect GSTM2 expression, with berberrubine and resveratrol being the most effective. Furthermore, it was found that a DNA methylation inhibitor and berberrubine can influence the methylation level of the GSTM2 gene.
Glutathione S-transferases (GSTs) belong to one class of phase 2 detoxification enzymes which are important in metabolism and/or detoxification of various electrophilic endogenous metabolites and xenobiotics. From the available database, we found that GSTM2 gene expression is lower in high stages of bladder urothelial carcinoma than in stage 1 and normal bladder tissue. GSTM2 overexpression retards invasion, migration and tumor sphere formation of bladder cancer cells. Analysis of GSTM2 promoter activity shows that one SP1 site located at - 48 to - 40 bp is important for GSTM2 gene expression in BFTC 905 cells. An SP1 inhibitor, mithramycin A, inhibits GSTM2 promoter activity and protein expression. SP1 overexpression also increases GSTM2 expression in BFTC 905 and 5637 cells. Eight potential phytochemicals were analyzed for GSTM2 promoter activation, and results indicated that baicalein, berberrubine, chalcone, curcumin, resveratrol, and wogonin can increase promoter activity. In endogenous GSTM2 expression, berberrubine and resveratrol activated GSTM2 mRNA and protein expression the most. A DNA methylation inhibitor, 5-aza-deoxycytidine, can decrease GSTM2 gene methylation level and then increase its gene expression; 50 mu M berberrubine decreased the GSTM2 gene methylation level, providing a mechanism for activating GSTM2 gene expression. Berberrubine and resveratrol also increased SP1 protein expression as one of the mechanisms for GSTM2 gene expression. In summary, berberrubine and resveratrol activates GSTM2 expression which inhibits cell proliferation, migration, and invasion of bladder cancer cells. The GSTM2 expression mechanism is partially via SP1 activation, and the effect of berberrubine is also partly via DNA CpG demethylation.

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