Skip to main content

Advertisement

Log in

Pre-mir-27a rs895819 polymorphism and cancer risk: a meta-analysis

  • Published:
Molecular Biology Reports Aims and scope Submit manuscript

Abstract

Aberrant expression of miRNAs plays critical roles in cancer development. Single nucleotide polymorphism (SNP) in miRNA precursors may affect miRNA expression levels. An important SNP in the pre-mir-27a with a A to G change (rs895819) was identified. Several original studies have explored the role of this SNP in cancer risk, but the results of these studies remain conflicting rather than conclusive. Therefore, we performed a meta-analysis of the published studies to derive a more precise estimation of the association between pre-mir-27a rs895819 polymorphism and cancer risk. In this meta-analysis, a total of 6 case–control studies (including 3,255 cases and 4,181 controls) were analyzed. The results of the overall meta-analysis did not suggest any associations between pre-mir-27a rs895819 polymorphism and cancer susceptibility. However, an decreased risk was observed in the subgroup of breast cancer patients (G vs A: OR = 0.90, 95 % CI = 0.83 ~ 0.97; P heterogeneity  = 0.75) or in the subgroup of Caucasian race (G vs A: OR = 0.90, 95 % CI = 0.83 ~ 0.97, P heterogeneity  = 0.78, I 2 = 0; AG vs AA: OR = 0.84, 95 % CI = 0.75 ~ 0.94, P heterogeneity  = 0.35, I 2 = 3.7 %; GG+AG vs AA: OR = 0.85, 95 % CI = 0.76 ~ 0.94, P heterogeneity  = 0.48, I 2 = 0). The findings suggest that pre-mir-27a rs895819 polymorphism may have some relation to breast cancer susceptibility or cancer development in Caucasian.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Siegel R, Naishadham D, Jemal A (2012) Cancer statistics, 2012. CA Cancer J Clin 62:10–29

    Article  PubMed  Google Scholar 

  2. Lichtenstein P et al (2000) Environmental and heritable factors in the causation of cancer–analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 343:78–85

    Article  PubMed  CAS  Google Scholar 

  3. He L, Hannon GJ (2004) MicroRNAs: small RNAs with a big role in gene regulation. Nat Rev Genet 5:522–531

    Article  PubMed  CAS  Google Scholar 

  4. Anglicheau D, Muthukumar T, Suthanthiran M (2010) MicroRNAs: small RNAs with big effects. Transplantation 90:105–112

    Article  PubMed  CAS  Google Scholar 

  5. Kutanzi KR et al (2011) MicroRNA-mediated drug resistance in breast cancer. Clin Epigenetics 2:171–185

    Article  PubMed  CAS  Google Scholar 

  6. Esquela-Kerscher A, Slack FJ (2006) Oncomirs-microRNAs with a role in cancer. Nat Rev Cancer 6:259–269

    Article  PubMed  CAS  Google Scholar 

  7. Yang R et al (2009) A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk. Breast Cancer Res Treat 121:693–702

    Article  PubMed  Google Scholar 

  8. Sun Q et al (2010) Hsa-mir-27a genetic variant contributes to gastric cancer susceptibility through affecting miR-27a and target gene expression. Cancer Sci 101:2241–2247

    Article  PubMed  CAS  Google Scholar 

  9. Catucci I et al (2012) The SNP rs895819 in miR-27a is not associated with familial breast cancer risk in Italians. Breast Cancer Res Treat 133:805–807

    Article  PubMed  Google Scholar 

  10. Hezova R et al (2012) Evaluation of SNPs in miR-196-a2, miR-27a and miR-146a as risk factors of colorectal cancer. World J Gastroenterol 18:2827–2831

    Article  PubMed  CAS  Google Scholar 

  11. Zhang M et al (2012) Associations of miRNA polymorphisms and female physiological characteristics with breast cancer risk in Chinese population. Eur J Cancer Care (Engl) 21:274–280

    Article  CAS  Google Scholar 

  12. Zhou Y et al (2012) Association analysis of genetic variants in microRNA networks and gastric cancer risk in a Chinese Han population. J Cancer Res Clin Oncol 138:939–945

    Article  PubMed  CAS  Google Scholar 

  13. Mantel N, Haenszel W (1959) Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 22:719–748

    PubMed  CAS  Google Scholar 

  14. DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7:177–188

    Article  PubMed  CAS  Google Scholar 

  15. Egger M et al (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315:629–634

    Article  PubMed  CAS  Google Scholar 

  16. Yang R, Burwinkel B (2012) A bias in genotyping the miR-27a rs895819 and rs11671784 variants. Breast Cancer Res Treat 134:899–901

    Article  PubMed  CAS  Google Scholar 

  17. Mertens-Talcott SU et al (2007) The oncogenic microRNA-27a targets genes that regulate specificity protein transcription factors and the G2-M checkpoint in MDA-MB-231 breast cancer cells. Cancer Res 67:11001–11011

    Article  PubMed  CAS  Google Scholar 

  18. Li X et al (2010) MicroRNA-27a indirectly regulates estrogen receptor alpha expression and hormone responsiveness in MCF-7 breast cancer cells. Endocrinology 151:2462–2473

    Article  PubMed  CAS  Google Scholar 

  19. Chintharlapalli S et al (2011) Betulinic acid inhibits colon cancer cell and tumor growth and induces proteasome-dependent and -independent downregulation of specificity proteins (Sp) transcription factors. BMC Cancer 11:371

    Article  PubMed  CAS  Google Scholar 

  20. Guttilla IK, White BA (2009) Coordinate regulation of FOXO1 by miR-27a, miR-96, and miR-182 in breast cancer cells. J Biol Chem 284:23204–23216

    Article  PubMed  CAS  Google Scholar 

  21. Zhou L et al (2012) Mechanism and function of decreased FOXO1 in renal cell carcinoma. J Surg Oncol 105:841–847

    Article  PubMed  CAS  Google Scholar 

  22. Ma Y et al (2010) miR-27a regulates the growth, colony formation and migration of pancreatic cancer cells by targeting Sprouty2. Cancer Lett 298:150–158

    Article  PubMed  CAS  Google Scholar 

  23. Lerner M et al (2011) MiRNA-27a controls FBW7/hCDC4-dependent cyclin E degradation and cell cycle progression. Cell Cycle 10:2172–2183

    Article  PubMed  CAS  Google Scholar 

  24. Spruck C (2011) miR-27a regulation of SCF(Fbw7) in cell division control and cancer. Cell Cycle 10:3232–3233

    Article  PubMed  CAS  Google Scholar 

  25. Wang Q et al (2011) Upregulation of miR-27a contributes to the malignant transformation of human bronchial epithelial cells induced by SV40 small T antigen. Oncogene 30:3875–3886

    Article  PubMed  CAS  Google Scholar 

  26. Fletcher CE et al (2012) Androgen-regulated processing of the oncomir MiR-27a, which targets prohibitin in prostate cancer. Hum Mol Genet 21:3112–3127

    Article  PubMed  CAS  Google Scholar 

  27. Liu T et al (2009) MicroRNA-27a functions as an oncogene in gastric adenocarcinoma by targeting prohibitin. Cancer Lett 273:233–242

    Article  PubMed  CAS  Google Scholar 

  28. Jazdzewski K et al (2008) Common SNP in pre-miR-146a decreases mature miR expression and predisposes to papillary thyroid carcinoma. Proc Natl Acad Sci USA 105:7269–7274

    Article  PubMed  CAS  Google Scholar 

  29. Duan R, Pak C, Jin P (2007) Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA. Hum Mol Genet 16:1124–1131

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This study was supported by the National Natural Science Foundation of China (81272470).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jianhua Zhao.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (XLS 17 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhong, S., Chen, Z., Xu, J. et al. Pre-mir-27a rs895819 polymorphism and cancer risk: a meta-analysis. Mol Biol Rep 40, 3181–3186 (2013). https://doi.org/10.1007/s11033-012-2392-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11033-012-2392-3

Keywords

Navigation