Current knowledge of microRNA-mediated regulation of drug metabolism in humans
被引:45
|
作者:
Nakano, Masataka
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机构:
Kanazawa Univ, Fac Pharmaceut Sci, WPI Nano Life Sci Inst WPI NanoLSI, Drug Metab & Toxicol, Kanazawa, Ishikawa, Japan
Japan Soc Promot Sci, Tokyo, JapanKanazawa Univ, Fac Pharmaceut Sci, WPI Nano Life Sci Inst WPI NanoLSI, Drug Metab & Toxicol, Kanazawa, Ishikawa, Japan
Nakano, Masataka
[1
,2
]
Nakajima, Miki
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机构:
Kanazawa Univ, Fac Pharmaceut Sci, WPI Nano Life Sci Inst WPI NanoLSI, Drug Metab & Toxicol, Kanazawa, Ishikawa, JapanKanazawa Univ, Fac Pharmaceut Sci, WPI Nano Life Sci Inst WPI NanoLSI, Drug Metab & Toxicol, Kanazawa, Ishikawa, Japan
Nakajima, Miki
[1
]
机构:
[1] Kanazawa Univ, Fac Pharmaceut Sci, WPI Nano Life Sci Inst WPI NanoLSI, Drug Metab & Toxicol, Kanazawa, Ishikawa, Japan
Drug metabolism;
CYP;
UGT;
SULT;
microRNA;
post-transcriptional regulation;
PREGNANE X RECEPTOR;
FUNCTIONAL GENOMICS APPROACH;
MESSENGER-RNA LEVELS;
CANCER CELL-LINES;
HUMAN LIVER-CELLS;
HUMAN HEPATOCYTES;
UDP-GLUCURONOSYLTRANSFERASES;
3'-UNTRANSLATED REGION;
GENETIC POLYMORPHISMS;
POSTTRANSCRIPTIONAL REGULATION;
D O I:
10.1080/17425255.2018.1472237
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Introduction: Understanding the factors causing inter- and intra-individual differences in drug metabolism potencies is required for the practice of personalized or precision medicine, as well as for the promotion of efficient drug development. The expression of drug-metabolizing enzymes is controlled by transcriptional regulation by nuclear receptors and transcriptional factors, epigenetic regulation, such as DNA methylation and histone acetylation, and post-translational modification. In addition to such regulation mechanisms, recent studies revealed that microRNAs (miRNAs), endogenous similar to 22-nucleotide non-coding RNAs that regulate gene expression through the translational repression and degradation of mRNAs, significantly contribute to post-transcriptional regulation of drug-metabolizing enzymes. Areas covered: This review summarizes the current knowledge regarding miRNAs-dependent regulation of drug-metabolizing enzymes and transcriptional factors and its physiological and clinical significance. We also describe recent advances in miRNA-dependent regulation research, showing that the presence of pseudogenes, single-nucleotide polymorphisms, and RNA editing affects miRNA targeting. Expert opinion: It is unwavering fact that miRNAs are critical factors causing inter- and intra-individual differences in the expression of drug-metabolizing enzymes. Consideration of miRNA-dependent regulation would be a helpful tool for optimizing personalized and precision medicine.
机构:
Shanxi Univ, Inst Appl Chem, Taiyuan, Peoples R China
Shanxi Univ, Modern Res Ctr Tradit Chinese Med, Key Lab Chem Biol & Mol Engn, Minist Educ, Taiyuan, Peoples R ChinaShanxi Univ, Inst Appl Chem, Taiyuan, Peoples R China
Jiang, Shan
Cui, Jin-Long
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Shanxi Univ, Inst Appl Chem, Taiyuan, Peoples R ChinaShanxi Univ, Inst Appl Chem, Taiyuan, Peoples R China
Cui, Jin-Long
Li, Xiao-ke
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机构:
Shanxi Univ, Inst Appl Chem, Taiyuan, Peoples R China
Shanxi Univ, Modern Res Ctr Tradit Chinese Med, Key Lab Chem Biol & Mol Engn, Minist Educ, Taiyuan, Peoples R ChinaShanxi Univ, Inst Appl Chem, Taiyuan, Peoples R China
机构:
Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
Stanford Univ, Dept Genet, Stanford, CA 94305 USAStanford Univ, Dept Pediat, Stanford, CA 94305 USA
Roy-Chaudhuri, Biswajoy
Valdmanis, Paul N.
论文数: 0引用数: 0
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机构:
Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
Stanford Univ, Dept Genet, Stanford, CA 94305 USAStanford Univ, Dept Pediat, Stanford, CA 94305 USA
Valdmanis, Paul N.
Zhang, Yue
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机构:
Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
Stanford Univ, Dept Genet, Stanford, CA 94305 USAStanford Univ, Dept Pediat, Stanford, CA 94305 USA
Zhang, Yue
Wang, Qing
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机构:
Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
Stanford Univ, Dept Genet, Stanford, CA 94305 USAStanford Univ, Dept Pediat, Stanford, CA 94305 USA
Wang, Qing
Luo, Qing-Jun
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机构:
Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
Stanford Univ, Dept Genet, Stanford, CA 94305 USAStanford Univ, Dept Pediat, Stanford, CA 94305 USA
Luo, Qing-Jun
Kay, Mark A.
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机构:
Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
Stanford Univ, Dept Genet, Stanford, CA 94305 USAStanford Univ, Dept Pediat, Stanford, CA 94305 USA
机构:
Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USAYale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
Kim, Minlee
Slack, Frank J.
论文数: 0引用数: 0
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机构:
Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USAYale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA