CYP3A

CYP3A
CYP3A
식별자
에일리어스CYP3A, 시토크롬 P450, 패밀리 3, 서브패밀리 A, CYP3
외부 IDGeneCards: CYP3A
맞춤법
종.인간마우스
엔트레즈

1574

없음

앙상블

없음

없음

유니프로트

n
a

없음

RefSeq(mRNA)

NM_000775

없음

RefSeq(단백질)

없음

없음

장소(UCSC)없음없음
PubMed 검색[1]없음
위키데이터
인간 보기/편집

CYP3A로도 알려진 시토크롬 P450, 패밀리 3, 서브 패밀리 A는 인간 유전자 궤적입니다.[2][3]생쥐에게서 상동성 궤적을 찾을 수 있다.[4]

CYP3A 궤적은 유전자의 시토크롬 P450 슈퍼패밀리의 3A 서브패밀리의 알려진 모든 구성원을 포함합니다.이 유전자들은 약물 대사 및 콜레스테롤, 스테로이드 및 기타 지질 합성과 관련된 많은 반응을 촉매하는 모노옥시게나아제를 암호화한다.CYP3A 클러스터는 다음 4개의 유전자로 구성됩니다.

영역에는 다음 4개의 의사진도 포함되어 있습니다.

또한 이 지역에서 생산된 성적표에 포함되거나 포함되지 않을 수 있는 몇 가지 추가 엑손도 있습니다.이전에는 또 다른 CYP3A 멤버인 CYP3A3가 존재한다고 생각되었지만, 현재는 이 시퀀스가 CYP3A4의 [2]전사 변형을 나타낸다고 생각됩니다.

레퍼런스

  1. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. ^ a b "Entrez Gene: CYP3A cytochrome P450, family 3, subfamily A".
  3. ^ Gellner K, Eiselt R, Hustert E, Arnold H, Koch I, Haberl M, et al. (March 2001). "Genomic organization of the human CYP3A locus: identification of a new, inducible CYP3A gene". Pharmacogenetics. 11 (2): 111–21. doi:10.1097/00008571-200103000-00002. PMID 11266076.
  4. ^ Zaphiropoulos PG (June 2003). "A map of the mouse Cyp3a locus". DNA Sequence. 14 (3): 155–62. doi:10.1080/1042517031000089478. PMID 14509827. S2CID 21317627.

추가 정보

  • Smith G, Stubbins MJ, Harries LW, Wolf CR (December 1998). "Molecular genetics of the human cytochrome P450 monooxygenase superfamily". Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 28 (12): 1129–65. doi:10.1080/004982598238868. PMID 9890157.
  • Lamba JK, Lin YS, Schuetz EG, Thummel KE (November 2002). "Genetic contribution to variable human CYP3A-mediated metabolism". Advanced Drug Delivery Reviews. 54 (10): 1271–94. doi:10.1016/S0169-409X(02)00066-2. PMID 12406645.
  • Finta C, Zaphiropoulos PG (December 2000). "The human cytochrome P450 3A locus. Gene evolution by capture of downstream exons". Gene. 260 (1–2): 13–23. doi:10.1016/S0378-1119(00)00470-4. PMID 11137287.
  • Miyazawa M, Shindo M, Shimada T (October 2001). "Roles of cytochrome P450 3A enzymes in the 2-hydroxylation of 1,4-cineole, a monoterpene cyclic ether, by rat and human liver microsomes". Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 31 (10): 713–23. doi:10.1080/00498250110065595. PMID 11695850. S2CID 41495172.
  • Reid JM, Kuffel MJ, Ruben SL, Morales JJ, Rinehart KL, Squillace DP, Ames MM (September 2002). "Rat and human liver cytochrome P-450 isoform metabolism of ecteinascidin 743 does not predict gender-dependent toxicity in humans". Clinical Cancer Research. 8 (9): 2952–62. PMID 12231541.
  • Martínez C, García-Martín E, Pizarro RM, García-Gamito FJ, Agúndez JA (September 2002). "Expression of paclitaxel-inactivating CYP3A activity in human colorectal cancer: implications for drug therapy". British Journal of Cancer. 87 (6): 681–6. doi:10.1038/sj.bjc.6600494. PMC 2364247. PMID 12237780.
  • Dowling TC, Briglia AE, Fink JC, Hanes DS, Light PD, Stackiewicz L, Karyekar CS, Eddington ND, Weir MR, Henrich WL (May 2003). "Characterization of hepatic cytochrome p4503A activity in patients with end-stage renal disease". Clinical Pharmacology and Therapeutics. 73 (5): 427–34. doi:10.1016/S0009-9236(03)00056-0. PMID 12732843. S2CID 23774236.
  • Sunman JA, Hawke RL, LeCluyse EL, Kashuba AD (March 2004). "Kupffer cell-mediated IL-2 suppression of CYP3A activity in human hepatocytes". Drug Metabolism and Disposition. 32 (3): 359–63. doi:10.1124/dmd.32.3.359. PMID 14977871.
  • Somogyi AA, Menelaou A, Fullston SV (October 2004). "CYP3A4 mediates dextropropoxyphene N-demethylation to nordextropropoxyphene: human in vitro and in vivo studies and lack of CYP2D6 involvement". Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 34 (10): 875–87. doi:10.1080/00498250400008371. PMID 15764408. S2CID 7680532.
  • Thompson EE, Kuttab-Boulos H, Yang L, Roe BA, Di Rienzo A (2006). "Sequence diversity and haplotype structure at the human CYP3A cluster". The Pharmacogenomics Journal. 6 (2): 105–14. doi:10.1038/sj.tpj.6500347. PMID 16314882.
  • Bochud M, Eap CB, Elston RC, Bovet P, Maillard M, Schild L, Shamlaye C, Burnier M (May 2006). "Association of CYP3A5 genotypes with blood pressure and renal function in African families". Journal of Hypertension. 24 (5): 923–9. doi:10.1097/01.hjh.0000222763.84605.4a. PMID 16612255. S2CID 30703443.
  • Cheung CY, Op den Buijsch RA, Wong KM, Chan HW, Chau KF, Li CS, Leung KT, Kwan TH, de Vrie JE, Wijnen PA, van Dieijen-Visser MP, Bekers O (June 2006). "Influence of different allelic variants of the CYP3A and ABCB1 genes on the tacrolimus pharmacokinetic profile of Chinese renal transplant recipients". Pharmacogenomics. 7 (4): 563–74. doi:10.2217/14622416.7.4.563. PMID 16753004.
  • Rais N, Chawla YK, Kohli KK (June 2006). "CYP3A phenotypes and genotypes in North Indians". European Journal of Clinical Pharmacology. 62 (6): 417–22. doi:10.1007/s00228-006-0105-3. PMID 16758258. S2CID 24149704.
  • Kirby B, Kharasch ED, Thummel KT, Narang VS, Hoffer CJ, Unadkat JD (November 2006). "Simultaneous measurement of in vivo P-glycoprotein and cytochrome P450 3A activities". Journal of Clinical Pharmacology. 46 (11): 1313–9. doi:10.1177/0091270006292625. PMID 17050796.
  • He P, Court MH, Greenblatt DJ, von Moltke LL (November 2006). "Human pregnane X receptor: genetic polymorphisms, alternative mRNA splice variants, and cytochrome P450 3A metabolic activity". Journal of Clinical Pharmacology. 46 (11): 1356–69. doi:10.1177/0091270006292125. PMID 17050801.
  • Watanabe A, Nakamura K, Okudaira N, Okazaki O, Sudo K (July 2007). "Risk assessment for drug-drug interaction caused by metabolism-based inhibition of CYP3A using automated in vitro assay systems and its application in the early drug discovery process". Drug Metabolism and Disposition. 35 (7): 1232–8. doi:10.1124/dmd.107.015016. PMID 17392390. S2CID 11204475.
  • Kharasch ED, Walker A, Isoherranen N, Hoffer C, Sheffels P, Thummel K, Whittington D, Ensign D (October 2007). "Influence of CYP3A5 genotype on the pharmacokinetics and pharmacodynamics of the cytochrome P4503A probes alfentanil and midazolam". Clinical Pharmacology and Therapeutics. 82 (4): 410–26. doi:10.1038/sj.clpt.6100237. PMID 17554244. S2CID 25122764.


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