[1] Zär ZM, Eloranta JJ, Stieger B, et al. Pharmacogenetics of OATP (SLC21 SLCO), OAT and OCT (SLC22) and PEPT (SLC15) transporters in the intestine, liver and kidney[J]. Pharmacogenomics, 2008, 9(5): 597-624. [2] Tamai I, Nezu J, Uchino H, et al. Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family[J]. Biochem Biophys Res Commun, 2000, 273(1): 251-260. [3] Abe T, Kakyo M, Tokui T, et al. Identification of a novel gene family encoding human liver-specific organic anion transporter LST-1[J]. J Biol Chem, 1999, 274 (24): 17159-17163. [4] Hsiang B, Zhu Y, Wang Z, et al. A novel human hepatic organic anion transporting polypeptide (OATP2). Identification of a liver specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl-CoA reductase inhibitor transporters[J]. J Biol Chem, 1999, 274(52): 37161-37168. [5] Nakai D, Nakagomi R, Furuta Y, et al. Human liverspecific organic anion transporter, LST-1, mediates uptake of pravastatin by human hepatocytes[J]. J Pharmacol Exp Ther, 2001, 297(3): 861-867. [6] Shitara Y, Itoh T, Sato H, et al. Inhibition of transportermediated hepatic uptake as a mechanism for drug-drug interaction between cerivastatin and cyclosporine A[J]. J Pharmacol Exp Ther, 2003, 304(2): 610-616. [7] Bolego C, Poli A, Cignarella A, et al. Novel statins: pharmacological and clinical results[J]. Cardiovasc Drugs Ther, 2002, 16(3): 251-257. [8] Niemi M. Role of OATP transporters in the disposition of drugs[J]. Pharmacogenomics, 2007, 8(7): 787-802. [9] Xu LY, He YJ, Zhang W, et al. Organic anion transporting polypeptide-1B1 haplotypes in Chinese patients[J]. Acta Pharmacol Sin, 2007, 28(10): 1693-1697. [10] Richard B. Kim, 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors (statins) and genetic variability (single nucleotide polymorphisms) in a hepatic drug uptake transporter: what's it all about[J]. Clin Pharmacol Ther, 2004, 75(5): 381-385. [11] PasanenMK, Neuvonen PJ, Niemi M. Global analysis of genetic variation in SLCO1B1[J]. Pharmacogenomics, 2008, 9(1): 19-33. [12] Nozawa T, Nakajima M, Tamai I, et al. Genetic polymorphisms of human organic anion transporters OATP-C (SLC21A6) and OATP-B (SLC21A9): allele frequencies in the Japanese population and functional analysis[J]. J Pharmacol Exp Ther, 2002, 302(2): 804-813. [13] Tirona RG, Leake BF, Merino G, et al. Polymorphisms in OATP-C: identification of multiple allelic variants associated with altered transport activity among European-and African-Americans[J]. J Biol Chem, 2001, 276 (38): 35669-35675. [14] Kameyama Y, Yamashita K, Kobayashi K, et al. Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1 *5, SLCO1B1 *15 and SLCO1B1 * 15 + C1007G, by using transient expression systems of HeLa and HEK293 cells[J]. Pharmacogenet Genomics, 2005, 15(7): 513-522. [15] Nishizato Y, Ieiri I, Suzuki H, et al. Polymorphisms of OATP-C (SLC21A6) and OAT3 (SLC22A8) genes: consequences for pravastatin pharmacokinetics[J]. Clin Pharmacol Ther, 2003, 73(6): 554-565. [16] Mwinyi J, Johne A, Bauer S, et al. Evidence for inverse effects of OATP-C (SLC21A6) *5 and *1b haplotypes on pravastatin kinetics[J]. Clin Pharmacol Ther, 2004, 75 (5): 415-421. [17] Niemi M, Schaeffeler E, Lang T, et al. High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)[J]. Pharmacogenetics, 2004, 14(7): 429-440. [18] Simonson SG, Raza A, Martin PD, et al. Rosuvastatin pharmacokinetics in heart transplant recipients administered an antirejection regimen including cyclosporine[J]. Clin Pharmacol Ther, 2004, 76(2): 167-177. [19] Lee E, Ryan S, Birmingham B, et al. Rosuvastatin pharmacokinetics and pharmacogenetics in white and Asian subjects residing in the same environment[J]. Clin Pharmacol Ther, 2005, 78(4): 330-341. [20] Hirano M, Maeda K, Shitara Y, et al. Contribution of OATP2 (OATP1B1) and OATP8 (OATP1B3) to the hepatic uptake of pitavastatin in humans[J]. J Pharmacol Exp Ther, 2004, 311(1): 139-146. [21] Chung JY, Cho JY, Yu KS, et al. Effect of OATP1B1 (SLCO1B1) variant alleles on the pharmacokinetics of pitavastatin in healthy volunteers[J]. Clin Pharmacol Ther, 2005, 78(4): 342-350. [22] Niemi M, Backman JT, Kajosaari LI, et al. Polymorphic organic anion transporting polypeptide 1B1 is a major determinant of repaglinide pharmacokinetics[J]. Clin Pharmacol Ther, 2005, 77(6): 468-478. [23] Zhang W, He YJ, Han CT, et al. Effect of SLCO1B1 genetic polymorphism on the pharmacokinetics of nateglinide [J]. Br J Clin Pharmacol, 2006, 62(5): 567-572. [24] Nozawa T, Minami H, Sugiura S, et al. Role of organic anion transporter OATP1B1 (OATP-C) in hepatic uptake of irinotecan and its active metabolite, 7-ethyl-10-hydroxycamptothecin: in vitro evidence and effect of single nucleotide polymorphisms[J]. Drug Metab Dispos, 2005, 33 (3): 434-439. [25] Han JY, Lim HS, Shin ES, et al. Influence of the organic anion-transporting polypeptide 1B1 (OATP1B1) polymorphisms on irinotecan-pharmacokinetics and clinical outcome of patients with advanced non-small cell lung cancer [J]. Lung Cancer, 2008, 59(1): 69-75. [26] Takane H, Miyata M, Burioka N, et al. Severe toxicities after irinotecan-based chemotherapy in a patient with lung cancer: a homozygote for the SLCO1B1 *15 allele[J]. Ther Drug Monit, 2007, 29(5): 666-668. [27] Morimoto K, Oishi T, Ueda S, et al. A novel variant allele of OATP-C (SLCO1B1) found in a Japanese patient with pravastatin-induced myopathy[J]. Drug Metab Pharmacokinet, 2004, 19(6): 453-455. [28] Zineh I. Pharmacogenetics of response to statins[J]. Curr Atheroscler Rep, 2007, 9(3): 187-194. [29] Cui Y, Konig J, Leier I, et al. Hepatic uptake of bilirubin and its conjugates by the human organic anion transporter SLC21A6[J]. J Biol Chem, 2001, 276(13): 9626-9630. [30] Ieiri I, Suzuki H, Kimura M, et al. Influence of common variants in the pharmacokinetic genes (OATP1B1, UGT1A1, andMRP2) on serum bilirubin levels in healthy subjects[J]. Hepatol Res, 2004, 30(4): 91-95. [31] Huang MJ, Kua KE, Teng HC, et al. Risk factors for severe hyperbilirubinemia in neonates[J]. Pediatr Res, 2004, 56(5): 682-689. [32] Zhang W, Chen BL, Ozdemir V, et al. SLCO1B1 521T->C functional genetic polymorphism and lipid-lowering efficacy of multiple-dose pravastatin in Chinese coronary heart disease patients[J]. Br J Clin Pharmacol, 2007, 64 (3): 346-352. [33] Iimori RT, Tabara Y, Kusuhara H, et al. Effect of genetic polymorphism of OATP-C (SLCO1B1) on the lipid-lowering response to HMG-CoA reductase inhibitors[J]. Drug Metab Pharmacokin, 2004, 19(5): 375-380. [34] Morimoto K, Ueda S, Seki N, et al. Candidate gene approach for the study of genetic factors involved in HMGCoA reductase inhibitor-induced rhabdomyolysis[R]. 18th JSSX annual meeting, Sapporo, Japan, 2003: 8PE-32. [35] Niemi M, Kivisto KT, Hofmann U, et al. Fexofenadine pharmacokinetics are associated with a polymorphism of the SLCO1B1 gene (encoding OATP1B1) [J]. Br J Clin Pharmacol, 2005, 59(5): 602-604. [36] Niemi M, Neuvonen PJ, Hofmann U, et al. Acute effects of pravastatin on cholesterol synthesis are associated with SLCO1B1 (encoding OATP1B1) haplotype * 17[J]. Pharmacogenet Genomics, 2005, 15(5): 303-309. |