Skip to Content
Merck
  • Curcumin causes DNA damage and affects associated protein expression in HeLa human cervical cancer cells.

Curcumin causes DNA damage and affects associated protein expression in HeLa human cervical cancer cells.

Oncology reports (2016-08-09)
Hung-Sheng Shang, Chuan-Hsun Chang, Yu-Ru Chou, Ming-Yang Yeh, Man-Kuan Au, Hsu-Feng Lu, Yung-Lin Chu, Hsiao-Min Chou, Hsiu-Chen Chou, Yung-Luen Shih, Jing-Gung Chung
ABSTRACT

Cervical cancer is one of the most common cancers in women worldwide and it is a prominent cause of cancer mortality. Curcumin is one of the major compounds from Turmeric and has been shown to induce cytotoxic cell death in human cervical cancer cells. However, there is no study to show curcumin induced DNA damage action via the effect on the DNA damage and repair protein in cervical cancer cells in detail. In this study, we investigated whether or not curcumin induced cell death via DNA damage, chromatin condensation in human cervical cancer HeLa cells by using comet assay and DAPI staining, respectively, we found that curcumin induced cell death through the induction of DNA damage, and chromatin condensation. Western blotting and confocal laser microscopy examination were used to examine the effects of curcumin on protein expression associated with DNA damage, repair and translocation of proteins. We found that curcumin at 13 µM increased the protein levels associated with DNA damage and repair, such as O6-methylguanine-DNA methyltransferase, early-onset breast cancer 1 (BRCA1), mediator of DNA damage checkpoint 1, p-p53 and p-H2A.XSer140 in HeLa cells. Results from confocal laser systems microscopy indicated that curcumin increased the translocation of p-p53 and p-H2A.XSer140 from cytosol to nuclei in HeLa cells. In conclusion, curcumin induced cell death in HeLa cells via induction of DNA damage, and chromatin condensation in vitro.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Monoclonal Anti-β-Actin antibody produced in mouse, clone AC-74, ascites fluid
Sigma-Aldrich
Monoclonal Anti-PARP antibody produced in mouse, clone C-2-10, ascites fluid
Sigma-Aldrich
Anti-MDC1 Antibody, clone P2B11, clone P2B11, from mouse