| Literature DB >> 30478904 |
Sai Kundur1, Amrita Prayag1, Priyanga Selvakumar1, Hung Nguyen1, Lloyd McKee1, Clairissa Cruz1, Asha Srinivasan1, Sunday Shoyele1, Ashakumary Lakshmikuttyamma1.
Abstract
Women with the breast cancer type 1 susceptibility protein (BRCA1) mutation and loss of BRCA1 expression are reported to have an increased risk of triple-negative breast cancer (TNBC). Targeting BRCA1 modulation might offer a therapeutic option to treat TNBC patients. Our studies detected that BRCA1 is poorly expressed in TNBC cell lines and highly expressed in ER+ breast cancer cell lines. To modulate BRCA1 expression, we tested two different dietary components to find out if any would induce tumor suppressor genes. We detected that quercetin and curcumin dose-dependently enhanced the BRCA1 expression. Further, a synergistic action of quercetin and curcumin was observed in modulating the BRCA1 level and in inhibiting the cell survival and migration of TNBC cell lines. Quercetin and curcumin appeared to induce BRCA1 promoter histone acetylation. Furthermore, BRCA1 knockdown induced cell survival and cell migration in ER + cells were significantly decreased by the combined treatment of quercetin and curcumin. Our present study concluded that the combination treatment of quercetin and curcumin acts synergistically to induce anticancer activity against TNBC cells by modulating tumor suppressor genes.Entities:
Keywords: EMT markers; drug resistance; flavonoids; triple-negative breast cancer
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Year: 2018 PMID: 30478904 DOI: 10.1002/jcp.27761
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384