Rižner Tea Lanišnik, Thalhammer Theresia, Özvegy-Laczka Csilla
Institute of Biochemistry, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia.
Department of Pathophysiology and Allergy Research, Centre for Pathophysiology, Infectiology and Immunology, Medical University of ViennaVienna, Austria.
Front Pharmacol. 2017 Jun 19;8:346. doi: 10.3389/fphar.2017.00346. eCollection 2017.
Endometrial and ovarian cancers predominately affect women after menopause, and are more frequently observed in developed countries. These are considered to be hormone-dependent cancers, as steroid hormones, and estrogens in particular, have roles in their onset and progression. After the production of estrogens in the ovary has ceased, estrogen synthesis occurs in peripheral tissues. This depends on the cellular uptake of estrone-sulfate and dehydroepiandrosterone-sulfate, as the most important steroid precursors in the plasma of postmenopausal women. The uptake through transporter proteins, such as those of the organic anion-transporting polypeptide (OATP) and organic anion-transporter (OAT) families, is followed by the synthesis and action of estradiol E2. Here, we provide an overview of the current understanding of this intracrine action of steroid hormones, which depends on the availability of the steroid precursors and transmembrane transporters for precursor uptake, along with the enzymes for the synthesis of E2. The data is also provided relating to the selected transmembrane transporters from the OATP, OAT, SLC51, and ABC-transporter families, and the enzymes involved in the E2-generating pathways in cancers of the endometrium and ovary. Finally, we discuss these transporters and enzymes as potential drug targets.
子宫内膜癌和卵巢癌主要影响绝经后的女性,在发达国家更为常见。这些被认为是激素依赖性癌症,因为类固醇激素,尤其是雌激素,在其发病和进展中起作用。卵巢停止产生雌激素后,外周组织会发生雌激素合成。这取决于硫酸雌酮和硫酸脱氢表雄酮作为绝经后女性血浆中最重要的类固醇前体的细胞摄取。通过转运蛋白(如有机阴离子转运多肽(OATP)和有机阴离子转运体(OAT)家族的转运蛋白)摄取后,会接着发生雌二醇E2的合成和作用。在此,我们概述了目前对类固醇激素这种内分泌作用的理解,它取决于类固醇前体和用于前体摄取的跨膜转运体的可用性,以及合成E2的酶。还提供了与来自OATP、OAT、SLC51和ABC转运体家族的选定跨膜转运体以及参与子宫内膜癌和卵巢癌中E2生成途径的酶相关的数据。最后,我们讨论这些转运体和酶作为潜在药物靶点的情况。