Differential expression of ABC transporters (MDR1, MRP1, BCRP) in developing human embryos
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- ATP-Binding Cassette Transporters biosynthesis genetics metabolism MeSH
- Embryonic Development genetics physiology MeSH
- Gene Expression MeSH
- Liver embryology MeSH
- Kidney embryology MeSH
- Humans MeSH
- Drug Resistance, Multiple MeSH
- ATP Binding Cassette Transporter, Subfamily B biosynthesis genetics metabolism MeSH
- Intestines embryology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- ATP-Binding Cassette Transporters MeSH
- ATP Binding Cassette Transporter, Subfamily B MeSH
Three ABC transporters (MDR1, MRP1, BCRP), belonging to the family of multidrug resistance (MDR) proteins, play a crucial role in the protection mechanisms during embryogenesis and mediate drug resistance in cancer cells. The distribution of these transporters in the series of human embryonal/fetal intestine, liver and kidneys of various stages of intrauterine development (IUD) by indirect two-step immunohistochemical method was investigated. The organ- and age-specific expression patterns of these transporters were depicted and compared with the expression in adult organs. The evaluation of intestine and liver samples demonstrate differences in expression pattern of ABC transporters during IUD. On the contrary, in kidneys the age-specific localization was not observed. However, the increasing positivity from the kidney surface towards deeper, more differentiated parts was found. Hopefully, our study may contribute to elucidation of the role of multidrug resistance (MDR) pathways during IUD in man.
See more in PubMed
J Exp Med. 1998 Sep 7;188(5):797-808 PubMed
Br J Pharmacol. 1998 May;124(2):416-24 PubMed
J Natl Cancer Inst. 2000 Oct 18;92(20):1651-6 PubMed
Dev Growth Differ. 2003 Aug;45(4):377-87 PubMed
Neoplasma. 2009;56(4):279-83 PubMed
Biochemistry. 1999 May 25;38(21):6887-96 PubMed
J Clin Invest. 1995 Oct;96(4):1698-705 PubMed
J Cell Physiol. 1993 Nov;157(2):392-402 PubMed
Cancer Res. 2004 Oct 15;64(20):7491-9 PubMed
Mol Pharm. 2009 Jan-Feb;6(1):134-43 PubMed
Proc Natl Acad Sci U S A. 2002 Sep 17;99(19):12339-44 PubMed
Carcinogenesis. 2008 Dec;29(12):2289-97 PubMed
Cancer Res. 2001 Apr 15;61(8):3458-64 PubMed
J Lipid Res. 2001 Jul;42(7):1007-17 PubMed
Am J Pathol. 1992 Nov;141(5):1063-72 PubMed
Proc Natl Acad Sci U S A. 1997 Mar 4;94(5):2031-5 PubMed
FEBS Lett. 2006 Feb 13;580(4):1103-11 PubMed
Pharm Res. 2004 May;21(5):719-35 PubMed
Biometals. 2005 Aug;18(4):349-58 PubMed
Drug Metab Dispos. 2009 Jan;37(1):203-10 PubMed
Dev Cell. 2009 Dec;17(6):755-73 PubMed
Kidney Int. 2008 Jan;73(2):220-5 PubMed
Ren Fail. 2001 May-Jul;23(3-4):331-7 PubMed