Dependence between estrogen sulfotransferase (SULT1E1) and nuclear transcription factor Nrf-2 regulations via oxidative stress in breast cancer

被引:4
作者
Nazmeen, Aarifa [1 ]
Chen, Guangping [2 ]
Maiti, Smarajit [1 ]
机构
[1] Oriental Inst Sci & Technol, Dept Biochem, Cell & Mol Therapeut Lab, Midnapore 721101, India
[2] Oklahoma Technol & Res Pk, Venture & OSU Lab, 1110 S Innovat Way, Stillwater, OK 74074 USA
关键词
Breast cancer; Oxidative stress; Estrogen regulations; REDOX REGULATION; RAT-LIVER; AUTOPHAGY; PROTEINS; P62; TRANSPORTERS; MECHANISMS; INDUCTION; SULFATION; HYPOXIA;
D O I
10.1007/s11033-020-05518-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human estrogen sulfotransferase (SULT1E1) and nuclear factor erythroid 2-related factor 2 (Nrf-2) expression influences each other in advanced human breast carcinogenesis. The difference in the metabolism of estradiol (E2) in pre- and post-menopausal women remains to be connected with post-menopausal breast cancer. A synergism between ROS production and E2 generation has been demonstrated. No definite mechanism for simultaneous functions of Nrf2, oxidative stress E2 regulating enzymes (SULT1E1) has been yet clarified. Our present review demonstrates that ROS dependent regulation of Nrf-2 is one of the most important determinants of E2 regulation by altering SULT1E1 expression. This study also focuses the idea that estrogen receptor cased subtypes of cancer may have different molecular environments which has an impact on the therapeutic efficacy.
引用
收藏
页码:4691 / 4698
页数:8
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