ASSOCIATION OF CERTAIN SINGLE NUCLEOTIDE POLYMORPHISM GENES OF APOPTOSIS SYSTEM WITH A RISK OF DEVELOPMENT OF COLORECTAL CANCER IN RUSSIAN POPULATION

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Abstract

Aim. Study the effect of single nucleotide polymorphism genes TP53 (rsl042522, rsl 800371), CDKN2A (rs3731217, rs3088440) and MDM2 (rs2279744) on the risk of development of colorectal cancer (CRC) in population of Perm Region. Materials and methods. Case group consisted of 198 patients with histologically verified CRC, control group - 205 individuals with CRC excluded by results of colonoscopy. DNA genotyping, obtained from leukocytes of venous blood of the studied individuals, was carried out by PCR with electrophoretic detection of results. Results. Significant inter-population differences of frequency of occurrence of alleles rs 1042522, rs3088440, rs2279744 in Russian population compared with East-Asian and European were detected (p<0.0001). Association of heterozygote (G/T) genotype rs2279744 with a lower risk of development of CRC regardless of sex and age (OR=0.51, 95% 0=0.26 - 0.97) was established. Statistically significant relations between development of CRC and other polymorphisms were not determined. Conclusion. Relations of gene polymorphism of apoptosis system with risk of development of CRC in Russian population was studied for the first time. The data obtained give evidence on the probable reduction of risk of development of CRC with carriage of heterozygote genotype of polymorphism rs2279744.

About the authors

M. Kh. Alyeva

Perm State Medical University

Author for correspondence.
Email: noemail@neicon.ru
Russian Federation

S. Ya. Zverev

Perm State Medical University; Perm Regional Centre for Prophylaxis and Control of AIDS and Infectious Diseases

Email: noemail@neicon.ru
Russian Federation

I. V. Feldblyum

Perm State Medical University

Email: noemail@neicon.ru
Russian Federation

E. Yu. Noskova

Perm Regional Centre for Prophylaxis and Control of AIDS and Infectious Diseases

Email: noemail@neicon.ru
Russian Federation

A. O. Kanina

Perm Regional Oncologic Dispensary

Email: noemail@neicon.ru
Russian Federation

N. I. Markovich

Federal Scientific Centre of Medical-Prophylaxis Technologies of Population Health Risk Management

Email: noemail@neicon.ru
Russian Federation

References

  1. Гухман В.Б. О планировании репрезентативных выборок данных в социальногуманитарных исследованиях. Вестник Тверского государственного технического университета. 2013, 2: 12-17.
  2. Имянитов Е.Н. Молекулярные механизмы опухолевого роста. Вопросы онкологии. 2010,2: 117-128.
  3. Петрова Г.В., Старинский В.В., Грецова О.П., Простое М.Ю. Показатели онкологической помощи больным колоректальным раком. Онкология. Журнал им. П.А. Герцена. 2013,6:41-43.
  4. Степанов В.А. Геномы, популяции, болезни: этническая геномика и персонифицированная медицина. Acta Naturae. 2010, 4: 18-31.
  5. Чумаков П.М. Белок р53 и его универсальные функции в многоклеточном организме. Успехи биологической химии. 2007, 47: 3-52.
  6. Dahabreh I.J., Linardou Н., Bouzika Р. et al. ТР53 Arg72Pro polymorphism and colorectal cancer risk: a systematic review and meta-analysis. Cancer Epidemiol. Biomarkers Prev. 2010, 19(7): 1840-1847.
  7. Li X., Dumont R, Della Pietra A. et al. The codon 47 polymorphism in p53 is functionally significant. J. Biol. Chem. 2005, 280 (25): 24245-24251.
  8. Ma X., Zhang B., Zheng W. Genetic variants associated with colorectal-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence. Gut. 2014, 63: 326-336.
  9. Migliorini G.,Fiege B.,Hosking F.J. et al. Variation at 10pl2.2 and 10pl4 influences risk of childhood В-cell acute lymphoblastic leukemia and phenotype. Blood. 2013, 122 (19): 3298-3307.
  10. Polakova V., Pardini B., Naccarati A. et al. Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic. Hum. Mutat. 2009, 30 (4): 661-668.
  11. QinX., Peng Q., Tang W. et al. An updated meta-analysis on the association of MDM2 SNP309 polymorphism with colorectal cancer risk. PLoS One. 2013, 8 (9): e76031.
  12. Sameer A.S., Shah Z.A., Syeed N. et al. TP53 Pro47Ser and Arg72Pro polymorphisms and colorectal cancer predisposition in an ethnic Kashmiri population. Genet. Mol. Res. 2010, 9 (2): 651-660.
  13. Theodoratou E., Montazeri Z., Hawken S. et al. Systematic meta-analyses and field synopsis of genetic association studies in colorectal cancer. J. Natl. Cancer Inst. 2012, 104 (19): 1433-1457.
  14. Wang J.J., Zheng Y., Sun L. et al. TP53 codon 72 polymorphism and colorectal cancer susceptibility: a meta-analysis. Mol. Biol. Rep. 2011, 38 (8): 4847-4853.

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Copyright (c) 2016 Alyeva M.K., Zverev S.Y., Feldblyum I.V., Noskova E.Y., Kanina A.O., Markovich N.I.

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