Abstract
Breast cancer resistance protein (BCRP), an adenosine triphosphate-binding cassette transporter, confers resistance to a series of anticancer reagents, including mitoxantrone, SN-38 and topotecan. In the present study, we found that estrone and 17β-estradiol potentiated the cytotoxicity of mitoxantrone, SN-38 and topotecan in BCRP-transduced K562 cells (K562/BCRP). These estrogens showed only a marginal effect, or none, in parental K562 cells. Estrone and 17β-estradiol increased the cellular accumulation of topotecan in K562/BCRP cells, but not in K562 cells, suggesting that these estrogens inhibit the BCRP-mediated drug efflux and overcome drug resistance.
Author supplied keywords
Cite
CITATION STYLE
Imai, Y., Tsukahara, S., Ishikawa, E., Tsuruo, T., & Sugimoto, Y. (2002). Estrone and 17β-estradiol reverse breast cancer resistance protein-mediated multidrug resistance. Japanese Journal of Cancer Research, 93(3), 231–235. https://doi.org/10.1111/j.1349-7006.2002.tb02162.x
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.