The Expression and Function of Organic Anion Transporting Polypeptides in Normal Tissues and in Cancer

被引:237
作者
Obaidat, Amanda [1 ]
Roth, Megan [1 ]
Hagenbuch, Bruno [1 ,2 ]
机构
[1] Univ Kansas, Med Ctr, Dept Pharmacol Toxicol & Therapeut, Kansas City, KS 66160 USA
[2] Univ Kansas, Ctr Canc, Kansas City, KS 66160 USA
来源
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 52 | 2012年 / 52卷
关键词
uptake transporter; cancer therapeutics; anticancer drugs; OATP; MESSENGER-RNA EXPRESSION; HUMAN BREAST-CARCINOMA; PREGNANE-X-RECEPTOR; BLOOD-BRAIN-BARRIER; HUMAN LIVER; HEPATOCELLULAR-CARCINOMA; OATP-B; PROSTAGLANDIN TRANSPORTER; HEPATIC TRANSPORTERS; HUMAN PLACENTA;
D O I
10.1146/annurev-pharmtox-010510-100556
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Organic anion transporting polypeptides (OATPs) are members of the SLCO gene superfamily of proteins. The 11 human OATPs are classified into 6 families and subfamilies on the basis of their amino acid sequence similarities. OATPs are expressed in several epithelial tissues throughout the body and transport mainly amphipathic molecules with molecular weights of more than 300 kDa. Members of the OATP1 and OATP2 families are functionally the best-characterized OATPs. Among these are the multispecific OATP1A2, OATP1B1, OATP1B3, and OATP2B1. They transport various endo- and xenobiotics, including hormones and their conjugates as well as numerous drugs such as several anticancer agents. Recent reports demonstrate that some OATPs are up- or downregulated in several cancers and that OATP expression might affect cancer development. On the basis of the findings summarized in this review, we propose that OATPs could be valuable targets for anticancer therapy.
引用
收藏
页码:135 / 151
页数:17
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