4.1 Article

Estrogen induces cell proliferation by promoting ABCG2-mediated efflux in endometrial cancer cells

Journal

BIOCHEMISTRY AND BIOPHYSICS REPORTS
Volume 16, Issue -, Pages 74-78

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ELSEVIER
DOI: 10.1016/j.bbrep.2018.10.005

Keywords

ABCG2; E-2; Cell proliferation; Tumorigenesis; Ishikawa cell

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Recently, it has reported that overeating of lipid-food has led to increase the amount of estrogen in vivo and the incidence of endometrial carcinomas. It is well-known that ATP-binding cassette transporter sub-family G2 (ABCG2) is highly expressed in cancer stem cells (CSCs). CSCs possess the ability for differentiation, tumorigenesis, stem cell self-renewal, and the efflux of anti-cancer drug and these abilities affect malignancy of cancer cells. However, little is known about the relationship between the expression of ABCG2 and malignancy of cancer cells. The present study aimed at understanding the regulatory mechanism underlying 17-beta-estradiol (E-2)-induced cell proliferation under the control of ABCG2. E-2 increased cell viability with a peak at 1 mu M and facilitated ABCG2 mRNA expression followed by the increase of ABCG2 expression level at plasma membrane. E-2-induced cell proliferation was inhibited by reserpine, an inhibitor of ABCG2, and the ABCG2 siRNA treatment. Thus, these results imply that ABCG2 plays an important role in the promotion of E-2-induced cell proliferation in Ishikawa cells.

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