Drug Transporters. Группа авторов

Чтение книги онлайн.

Читать онлайн книгу Drug Transporters - Группа авторов страница 61

Drug Transporters - Группа авторов

Скачать книгу

of which are excreted by the kidney. Although much of the original work in the field was based on in vitro data, in recent years a number of studies in Oat knockout mice, as well as analysis of the consequences of human SNPs, have cemented this view. Systems biology approaches applied to knockout mice metabolomics and transcriptomics data suggest a broader role for OATs in metabolism and signaling, including communication occurring between organs. This view is more fully expressed in the Remote Sensing and Signaling Theory, which may be relevant to both SLC and ABC “drug” transporters, as well as drug metabolizing enzymes.

      By understanding the mechanisms of these transporters, it may be possible to predict certain drug–drug interactions [88] and drug–metabolite interactions [88]. Regulation of OATs is a complicated process influenced by multiple intracellular signaling pathways and by various PTMs. Most studies have examined these regulatory factors in isolation. How they work in concert to modulate OAT function, to improve OAT‐related medical treatment, and to keep body homeostasis are important questions that will also provide insights into the workings of the remote sensing and signaling system.

      The authors would like to gratefully acknowledge Drs. Kevin T. Bush, Megha Nagle, David M. Truong, Vibha Bhatnagar, Gregory Kaler, Satish A. Eraly, and Wei Wu for their contributions to previous editions of this chapter. We also wish to thank other members of the Nigam lab who have, over many years, contributed to the material discussed here. Finally, we would like to thank Zhengxuan Liang, from Dr. You’s lab, for her help during the revision process.

      1 [1] Yan N. Structural advances for the major facilitator superfamily (MFS) transporters. Trends Biochem Sci (2013); 38 (3):151–159.

      2 [2] Bush K, Nagle M, Truong D, Bhatnagar V, Kaler G, Eraly S, Wu W, Nigam S. Drug transporters: molecular characterization and role in drug Disposition; 2014.

      3 [3] Nigam SK. What do drug transporters really do? Nat Rev Drug Discov 2015; 14 (1):29–44.

      4 [4] Nigam SK, Bush KT, Bhatnagar V. Drug and toxicant handling by the OAT organic anion transporters in the kidney and other tissues. Nat Clin Pract Nephrol 2007; 3 (8):443–448.

      5 [5] Eraly SA, Monte JC, Nigam SK. Novel slc22 transporter homologs in fly, worm, and human clarify the phylogeny of organic anion and cation transporters. Physiol Genomics 2004; 18 (1):12–24.

      6 [6] Wu W, Baker ME, Eraly SA, Bush KT, Nigam SK. Analysis of a large cluster of SLC22 transporter genes, including novel USTs, reveals species‐specific amplification of subsets of family members. Physiol Genomics 2009; 38 (2):116–124.

      7 [7] Koepsell H. The SLC22 family with transporters of organic cations, anions and zwitterions. Mol Aspects Med 2013; 34 (2–3):413–435.

      8 [8] Hediger MA, Clemencon B, Burrier RE, Bruford EA. The ABCs of membrane transporters in health and disease (SLC series): introduction. Mol Aspects Med 2013; 34 (2–3):95–107.

      9 [9] Engelhart DC, Granados JC, Shi D, Saier Jr MH, Baker ME, Abagyan R, Nigam SK. Systems biology analysis reveals eight SLC22 transporter subgroups, including OATs, OCTs, and OCTNs. Int J Mol Sci 2020; 21 (5):1791.

      10 [10] Nigam SK, Bush KT, Martovetsky G, Ahn S‐Y, Liu HC, Richard E, Bhatnagar V, Wu W. The organic anion transporter (OAT) family: a systems biology perspective. Physiol Rev 2015; 95 (1):83–123.

      11 [11] Nigam SK, Bush KT, Bhatnagar V, Poloyac SM, MomperJD. The systems biology of drug metabolizing enzymes and transporters: relevance to quantitative systems pharmacology. Clin Pharmacol Ther 2020; 108 (1):40–53.

      12 [12] Zhang J, Wang H, Fan Y, Yu Z, You G. Regulation of organic anion transporters: role in physiology, pathophysiology, and drug elimination. Pharmacol Ther 2020; 217:107647.

      13 [13] Srimaroeng C, Perry JL, Pritchard JB. Physiology, structure, and regulation of the cloned organic anion transporters. Xenobiotica 2008; 38 (7–8):889–935.

      14 [14] Sun W, Wu RR, van Poelje PD, Erion MD. Isolation of a family of organic anion transporters from human liver and kidney. Biochem Biophys Res Commun 2001; 283 (2):417–422.

      15 [15] Shin HJ, Anzai N, Enomoto A, He X, Kim DK, Endou H, Kanai Y. Novel liver‐specific organic anion transporter OAT7 that operates the exchange of sulfate conjugates for short chain fatty acid butyrate. Hepatology 2007; 45 (4):1046–1055.

      16 [16] Schömig E, Spitzenberger F, Engelhardt M, Martel F, Ording N, Gründemann D. Molecular cloning and characterization of two novel transport proteins from rat kidney. FEBS Lett 1998; 425 (1):79–86.

      17 [17] Yokoyama H, Anzai N, Ljubojevic M, Ohtsu N, Sakata T, Miyazaki H, Nonoguchi H, Islam R, Onozato ML, Tojo A, Tomita K, Kanai Y, Igarashi T, Sabolic I, Endou H. Functional and immunochemical characterization of a novel organic anion transporter Oat8 (Slc22a9) in rat renal collecting duct. Cell Physiol Biochem 2008; 21 (4):269–278.

      18 [18] Tsuchida H, Anzai N, Shin HJ, Wempe MF, Jutabha P, Enomoto A, Cha SH, Satoh T, Ishida M, Sakurai H, Endou H. Identification of a novel organic anion transporter mediating carnitine transport in mouse liver and kidney. Cell Physiol Biochem 2010; 25 (4–5):511–522.

      19 [19] Nishiwaki T, Daigo Y, Tamari M, Fujii Y, Nakamura Y. Molecular cloning, mapping, and characterization of two novel human genes, ORCTL3 and ORCTL4, bearing homology to organic‐cation transporters. Cytogenet Cell Genet 1998; 83 (3–4):251–255.

      20 [20] Bahn A, Hagos Y, Reuter S, Balen D, Brzica H, Krick W, Burckhardt BC, Sabolic I, Burckhardt G. Identification of a new urate and high affinity nicotinate transporter, hOAT10 (SLC22A13). J Biol Chem 2008; 283 (24):16332–16341.

      21 [21] Mori K, Ogawa Y, Ebihara K, Aoki T, Tamura N, Sugawara A, Kuwahara T, Ozaki S, Mukoyama M, Tashiro K, Tanaka I, Nakao K. Kidney‐specific expression of a novel mouse organic cation transporter‐like protein. FEBS Lett 1997; 417 (3):371–374.

      22 [22] Enomoto A, Kimura H, Chairoungdua A, Shigeta Y, Jutabha P, Cha SH, Hosoyamada M, Takeda M, Sekine T, Igarashi T, Matsuo H, Kikuchi Y, Oda T, Ichida K, Hosoya T, Shimokata K, Niwa T, Kanai Y, Endou H. Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Nature 2002; 417 (6887):447–452.

      23 [23] Burckhardt G, Burckhardt BC. in vitro and in vivo evidence of the importance of organic anion transporters (OATs) in drug therapy. In: Fromm MF, Kim RB, editor. Drug Transporters. Berlin Heidelberg: Springer; 2011. p 29–104.

      24 [24] VanWert AL, Gionfriddo MR, Sweet DH. Organic anion transporters: discovery, pharmacology, regulation and roles in pathophysiology. Biopharm Drug Dispos 2010; 31 (1):1–71.

      25 [25] Nigam SK. The SLC22 transporter family: a paradigm for the impact of drug transporters on metabolic pathways, signaling, and disease. Annu Rev Pharmacol Toxicol 2018; 58 (1):663–687.

      26 [26] Zhu C, Nigam KB, Date RC, Bush KT, Springer SA, Saier Jr MH, Wu W, Nigam SK. Evolutionary analysis and classification of OATs, OCTs, OCTNs, and other SLC22 transporters: structure‐function implications and analysis of sequence motifs. PLoS One 2015; 10 (11):e0140569.

      27 [27] Lee W, Ha J‐m, Sugiyama Y. Post‐translational regulation of the major drug transporters in the families of organic anion transporters and organic anion–transporting polypeptides. J Biol Chem 2020; 295 (50):17349–17364.

      28 [28] Simonson G, Vincent A, Roberg K, Huang Y, Iwanij V. Molecular cloning and characterization of a novel liver‐specific

Скачать книгу