THE XENOBIOTIC DETOXIFICATION SYSTEM IN THE THERAPY OF THREATENED ABORTION

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Issue: 
4
Year: 
2016

Professor O. Makarov (1), MD; S. Lunina (1); L. Salnikova (2), Biol. D; N. Lutsenko (1); V. Goncharova (1) 1 -N.I. Pirogov Russian National Research Medical University, Moscow 2 -N.I. Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow

Despite performed therapy for abortion, the highest risk of miscarriage was associated with a combination of the risky alleles of the ABCB1 and GSTP1 genes; the frequency of this combination was 13.2%.

Keywords: 
obstetrics and gynecology
miscarriage
xenobiotic detoxification gene polymorphisms
GSTP1
ABCB1
results of therapy



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References: 
  1. Sal'nikova L.E., Zamulaeva I.A., Belopol'skaja O.B. i dr. Vstrechaemost' TCR-mutantnyh limfotsitov u cheloveka v zavisimosti ot genotipov po loku-sam detoksikatsii ksenobiotikov // Ekologicheskaja genetika. – 2010; 8 (2): 18–23
  2. Bochkov N.P. Klinicheskaja genetika / M.: GEOTAR-Med, 2002; 457 s.2.
  3. Bansal T., Jaggi M., Khar R. et al. Emerging significance of flavonoids as P-glycoprotein inhibitors in cancer chemotherapy // J. Pharm. Pharmaceut. Sci. – 2009; 12 (1): 46–78.
  4. Diergaarde B., Potter J., Jupe E. et al. Polymorphisms in genes involved in sex hormone metabolism, estrogen plus progestin hormone therapy use, and risk of postmenopausal breast cancer // Cancer Epidemiol. Biomarkers Prev. – 2008; 17 (7): 1751–9
  5. Fertuck K., Matthews J., Zacharewski T. Hydroxylated benzo[a]pyrene metabolites are responsible for in vitro estrogen receptor-mediated gene expression induced by benzo[a]pyrene, but do not elicit uterotrophic effects in vivo // Toxicol. Sci. – 2001; 59 (2): 231–40.
  6. Hall M., Handley M., Gottesman M. Is resistance useless? Multidrug resistance and collateral sensitivity // Trends Pharmacol. Sci. – 2009; 30 (10): 546–56.
  7. Hamajima N. PCR–CTPP: a new genotyping technique in the era of genetic epidemiology // Exp. Rev. Mol. Diagn. – 2001; 1 (1): 119–23.
  8. Harbottle A., Daly A., Atherton K. et al. Role of glutathione S-transferase P1, P-glycoprotein and multidrug resistance-associated protein 1 in acquired doxorubicin resistance // Intern. J. Cancer. – 2001; 92 (6): 777–83.
  9. Josephy P. Genetic Variations in Human Glutathione Transferase Enzymes: . Significance for Pharmacology and Toxicology // Human Genom. Prot. Vol. – 2010 (2010), Article ID 876940, 14 pages doi:10.4061/2010/876940 URL: http://www.sage-hindawi.com/journals/hgp/2010/876940/
  10. Lamba J., Strom S., Venkataramanan R. et al. MDR1 genotype is associated with hepatic cytochrome P450 3A4 basal and induction phenotype // Clin. Pharmacol. Ther. – 2006; 79 (4): 325–38.
  11. Pasanen M. The expression and regulation of drug metabolism in human placenta // Adv. Drug Deliv. Rev. – 1999; 38: 81–97
  12. Schilling C., Gallicchio L., Miller S. et al. Genetic polymorphisms, hormone levels, and hot flashes in midlife women // Maturitas. – 2007; 57 (2): 120–31.
  13. Shimada T., Watanabe J., Sutter T. et al. Catalytic properties of polymorphic human cytochrome P450 1B1 variants // Carcinogenesis. – 1999; 20 (8): 1607–13.
  14. Van Lieshout E., Knapen M., Lange W. Localization of glutathione S-transferases alpha and pi in human embryonic tissues at 8 weeks gestational age // Human Reprod. – 1998; 13 (5): 1380–6.
  15. Guengerich F. Cytochrome P 450s, drugs and diseases // Mol. Interv. – 2003; 3 (4): 8–18.