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引用次数: 47
摘要
孕烷X受体(Pregnane X receptor, PXR)是一种孤儿核受体,可被多种内源性和外源性药物激活,包括化疗药物。PXR通过诱导药物代谢酶和药物转运蛋白,在肝脏和肠道的外源和内源性代谢和清除中发挥重要作用。然而,PXR在多种癌症组织中表达,越来越多的证据强烈地指出PXR在癌症生长和进展以及化疗结果中的差异作用。在癌细胞中,PXR除了调节参与药物代谢和转运的酶和蛋白的基因表达外,还调节其他参与增殖、转移、凋亡、抗凋亡、炎症和氧化应激的基因。在这篇综述中,我们将重点关注PXR在多种癌症中的不同作用,包括前列腺癌、乳腺癌、卵巢癌、子宫内膜癌和结肠癌。我们还讨论了进一步了解PXR在癌症中的不同作用的未来方向,并得出结论,需要鉴定新的选择性PXR调节剂来靶向PXR表达的癌症中的PXR。
Pregnane X Receptor and Cancer: Context-Specificity is Key.
Pregnane X receptor (PXR) is an adopted orphan nuclear receptor that is activated by a wide-range of endobiotics and xenobiotics, including chemotherapy drugs. PXR plays a major role in the metabolism and clearance of xenobiotics and endobiotics in liver and intestine via induction of drug-metabolizing enzymes and drug-transporting proteins. However, PXR is expressed in several cancer tissues and the accumulating evidence strongly points to the differential role of PXR in cancer growth and progression as well as in chemotherapy outcome. In cancer cells, besides regulating the gene expression of enzymes and proteins involved in drug metabolism and transport, PXR also regulates other genes involved in proliferation, metastasis, apoptosis, anti-apoptosis, inflammation, and oxidative stress. In this review, we focus on the differential role of PXR in a variety of cancers, including prostate, breast, ovarian, endometrial, and colon. We also discuss the future directions to further understand the differential role of PXR in cancer, and conclude with the need to identify novel selective PXR modulators to target PXR in PXR-expressing cancers.