Cytochrome P450 3A4, 3A5, and 2C8 expression in breast, prostate, lung, endometrial, and ovarian tumors: relevance for resistance to taxanes

被引:68
作者
van Eijk, Maarten [1 ]
Boosman, Rene J. [1 ]
Schinkel, Alfred H. [2 ]
Huitema, Alwin D. R. [1 ,3 ]
Beijnen, Jos H. [1 ,2 ,4 ]
机构
[1] Netherlands Canc Inst, Dept Pharm & Pharmacol, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Div Pharmacol, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[3] Univ Utrecht, Univ Med Ctr Utrecht, Dept Clin Pharm, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[4] Univ Utrecht, Div Pharmacoepidemiol & Clin Pharmacol, UIPS, Sci Fac, POB 80082, NL-3508 TB Utrecht, Netherlands
关键词
CYP; Paclitaxel; Docetaxel; Ritonavir; Intratumoral; HIV-1 PROTEASE INHIBITOR; PREGNANE-X RECEPTOR; MESSENGER-RNA; DOCETAXEL RESISTANCE; METABOLIZING-ENZYMES; IMMUNOHISTOCHEMICAL LOCALIZATION; P450-MEDIATED METABOLISM; BIOLOGICAL-ACTIVITY; TARGETED THERAPIES; CYP3A4; EXPRESSION;
D O I
10.1007/s00280-019-03905-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Enzymes of the cytochrome P450 (CYP) subfamily 3A and 2C play a major role in the metabolism of taxane anticancer agents. While their function in hepatic metabolism of taxanes is well established, expression of these enzymes in solid tumors may play a role in the in situ metabolism of drugs as well, potentially affecting the intrinsic taxane susceptibility of these tumors. This article reviews the available literature on intratumoral expression of docetaxel- and paclitaxel-metabolizing enzymes in mammary, prostate, lung, endometrial, and ovarian tumors. Furthermore, the clinical implications of the intratumoral expression of these enzymes are reviewed and the potential of concomitant treatment with protease inhibitors (PIs) as a method to inhibit CYP3A4-mediated metabolism is discussed.
引用
收藏
页码:487 / 499
页数:13
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