Clinical Research
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The Relationship Between miR-196a2 Polymorphism and Colorectal Cancer Risk

Year 2024, Volume: 7 Issue: 3, 348 - 352, 27.10.2024
https://doi.org/10.53446/actamednicomedia.1562372

Abstract

ABSTRACT
Objective
MicroRNAs are small endogenous, non-coding, single-stranded posttranscriptional RNA molecules. The discovery of microRNAs has made new contributions to cancer diagnosis and treatment. These microRNAs reported as a responsible for colorectal cancer development with several epigenetic changes. In this study, it was aimed to evaluate the relationship between the polymorphism of miR-196a-2 polymorphism rs11614913 and colorectal cancer in Turkish population.
Methods
Two hundred colorectal cancer patient (124 colon cancer and 76 rectal cancer) and 240 health control individuals were included in our study, which was planned as a hospital based retrospective cohort study. MiR-196a2 polymorphism in peripheral blood samples has been determined by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) method. Significance of the results has been evaluated by using SPSS (20.0 SPSS Inc., Chicago, IL, USA.) statistical program.
Results
miR-196a2 C / C + C / T genotypes was found to be associated with the risk of colorectal cancer development (p: 0.001; OR: 2.04, 95% CI: 1.293-3.236). The subgroup analysis, showed that the C / C + C / T genotype increased the risk of colon cancer development 2.11 times (p: 0.016; 95% CI: 1.136-3.918) and rectal cancer 2.86 times (p: 0.011; 95% CI:1.242-6.592). The relationship between any clinicopathological features of colorectal cancer and the frequency of the C / C + C / T genotype of miR196a2 was not statistically significant (p> 0.05).
Conclusion
This study supports that miR-196a2's C / C + C / T genotypes is related with increased colorectal cancer development risk.

References

  • Pan XM, Xiao X, Qin HJ, et al. MicroRNA variants and colorectal cancer risk: a meta-analysis. Genet Mol Res. 2016;15(3):10.4238/gmr.15038478.
  • Bayramov B, Bayramov N, Aslanov H, et al. Association of miR-149 T>C and miR-196a2 C>T Polymorphisms with Colorectal Cancer Susceptibility: A Case-Control Study. Biomedicines. 2023;11(9):2341.
  • Trujillo-Fernández YGV, Yzabal-Barbedillo C, Saucedo-Sarinaña AM, et al. Functional Variants in MicroRNAs (rs895819, rs11614913 and rs2910164) Are Associated with Susceptibility and Clinicopathological Features in Mexican Patients with Colorectal Cancer. Arch Iran Med. 2023;26(8):439-446.
  • Chen H, Sun LY, Chen LL, Zheng HQ, Zhang QF. A variant in microRNA-196a2 is not associated with susceptibility to and progression of colorectal cancer in Chinese. Intern Med J. 2012;42(6):e115-e119.
  • Yueh TC, Wang YC, Chin YT, et al. Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan. Int J Mol Sci. 2023;24(14):11613.
  • Gawish EA, Abu-Raia GY, Osheba I, et al. Association between miR-196a2 polymorphism and the development of hepatocellular carcinoma in the Egyptian population. Egypt Liver J. 2020;10:16.
  • Du W, Ma X, Kong W, et al. Association between rs11614913 polymorphism in miR-196a2 and colorectal cancer risk: a meta-analysis. Cancer Biomark. 2013;13(6):457-464.
  • Zhao H, Ming T, Tang S, et al. Wnt signaling in colorectal cancer: pathogenic role and therapeutic target. Mol Cancer. 2022;21(1):144.
  • Haerian MS, Haerian BS, Molanaei S, et al. MIR196A2 rs11614913 contributes to susceptibility to colorectal cancer in Iranian population: A multi-center case-control study and meta-analysis. Gene. 2018;669:82-90.
  • Xu L, Tang W. Associations of Polymorphisms in mir-196a2, mir-146a and mir-149 with Colorectal Cancer Risk: A Meta-Analysis. Pathol Oncol Res. 2016;22(2):261-267.
  • Kupcinskas J, Bruzaite I, Juzenas S, et al. Lack of association between miR-27a, miR-146a, miR-196a-2, miR-492 and miR-608 gene polymorphisms and colorectal cancer. Sci Rep. 2014;4:5993.
  • Coleman D, Kuwada S. miRNA as a Biomarker for the Early Detection of Colorectal Cancer. Genes. 2024; 15(3):338.
  • Ge J, Chen Z, Li R, Lu T, Xiao G. Upregulation of microRNA-196a and microRNA-196b cooperatively correlate with aggressive progression and unfavorable prognosis in patients with colorectal cancer. Cancer Cell Int. 2014;14(1):128.
  • Raue R, Frank AC, Syed SN, Brüne B. Therapeutic Targeting of MicroRNAs in the Tumor Microenvironment. Int J Mol Sci. 2021;22(4):2210.
  • Huang X, Zhu X, Yu Y, et al. Dissecting miRNA signature in colorectal cancer progression and metastasis. Cancer Lett. 2021;501:66-82.
  • Kulkarni B, Kirave P, Gondaliya P, et al. Exosomal miRNA in chemoresistance, immune evasion, metastasis and progression of cancer. Drug Discov Today. 2019;24(10):2058-2067.

MiR-196a2 Polimorfizmi ile Kolorektal Kanser Riski Arasındaki İlişki

Year 2024, Volume: 7 Issue: 3, 348 - 352, 27.10.2024
https://doi.org/10.53446/actamednicomedia.1562372

Abstract

ÖZ
Amaç
MicroRNA’lar küçük, endojen, kodlanmayan, tek sarmallı posttranskripsiyonel RNA molekülleridir. MikroRNA’ların keşfi, kanser teşhis ve tedavisine yeni katkılar sağlamıştır. Bu miRNA’ların çeşitli epigenetik değişiklerle kolorektal kanser gelişiminden sorumlu olduğu saptanmıştır. Bu çalışmada Türk toplumunda miR-196a2’nin rs11614913 polimorfizmi ile kolorektal kanser arasındaki ilişkinin değerlendirilmesi amaçlanmıştır.
Yöntem
Hastane bazlı retrospektif kohort çalşması olarak planlanan çalışmamıza 200 kolorektal kanser hastası (124 kolon kanseri ve 76 rektum kanseri) ve 240 sağlıklı kontrol bireyler dahil edilmiştir. Periferik kan örneklerinde miR-196a2 polimorfizmi, polimeraz zincir reaksiyonu ve restriksiyon fragman uzunluk polimorfizmi yöntemi ile belirlenmiştir. Sonuçların anlamlılığı SPSS (20.0 SPSS Inc., Chicago, IL, USA.) istatistik programı kullanılarak değerlendirilmiştir.
Bulgular
MiR-196a2 C/C + C/T genotiplerinin kolorektal kanser gelişim riski ile ilişkili olduğu saptanmıştır (p: 0.001; OR: 2.04, %95 CI: 1.293-3.236). Altgrup analizleri ise ise C/C+C/T genotipinin kolon kanseri gelişim riskini 2.11. kat (p: 0.016; %95 CI: 1.136-3.918) ve rektum kanserini ise 2.86 kat (p: 0.011; %95 CI: 1.242-6.592) arttırdığını göstermiştir. Kolorektal kanserin herhangi bir klinikopatolojik özelliği ile miR-196a2’nin C/C+ C/T genotipinin sıklığı arasında istatistiksel olarak anlamlı ilişki saptanmamıştır (p>0.05).
Sonuç
Bu çalışma miR-196a2'nin C / C + C / T genotiplerinin artmış kolorektal kanser gelişim riski ile ilişkili olduğunu desteklemektedir.

References

  • Pan XM, Xiao X, Qin HJ, et al. MicroRNA variants and colorectal cancer risk: a meta-analysis. Genet Mol Res. 2016;15(3):10.4238/gmr.15038478.
  • Bayramov B, Bayramov N, Aslanov H, et al. Association of miR-149 T>C and miR-196a2 C>T Polymorphisms with Colorectal Cancer Susceptibility: A Case-Control Study. Biomedicines. 2023;11(9):2341.
  • Trujillo-Fernández YGV, Yzabal-Barbedillo C, Saucedo-Sarinaña AM, et al. Functional Variants in MicroRNAs (rs895819, rs11614913 and rs2910164) Are Associated with Susceptibility and Clinicopathological Features in Mexican Patients with Colorectal Cancer. Arch Iran Med. 2023;26(8):439-446.
  • Chen H, Sun LY, Chen LL, Zheng HQ, Zhang QF. A variant in microRNA-196a2 is not associated with susceptibility to and progression of colorectal cancer in Chinese. Intern Med J. 2012;42(6):e115-e119.
  • Yueh TC, Wang YC, Chin YT, et al. Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan. Int J Mol Sci. 2023;24(14):11613.
  • Gawish EA, Abu-Raia GY, Osheba I, et al. Association between miR-196a2 polymorphism and the development of hepatocellular carcinoma in the Egyptian population. Egypt Liver J. 2020;10:16.
  • Du W, Ma X, Kong W, et al. Association between rs11614913 polymorphism in miR-196a2 and colorectal cancer risk: a meta-analysis. Cancer Biomark. 2013;13(6):457-464.
  • Zhao H, Ming T, Tang S, et al. Wnt signaling in colorectal cancer: pathogenic role and therapeutic target. Mol Cancer. 2022;21(1):144.
  • Haerian MS, Haerian BS, Molanaei S, et al. MIR196A2 rs11614913 contributes to susceptibility to colorectal cancer in Iranian population: A multi-center case-control study and meta-analysis. Gene. 2018;669:82-90.
  • Xu L, Tang W. Associations of Polymorphisms in mir-196a2, mir-146a and mir-149 with Colorectal Cancer Risk: A Meta-Analysis. Pathol Oncol Res. 2016;22(2):261-267.
  • Kupcinskas J, Bruzaite I, Juzenas S, et al. Lack of association between miR-27a, miR-146a, miR-196a-2, miR-492 and miR-608 gene polymorphisms and colorectal cancer. Sci Rep. 2014;4:5993.
  • Coleman D, Kuwada S. miRNA as a Biomarker for the Early Detection of Colorectal Cancer. Genes. 2024; 15(3):338.
  • Ge J, Chen Z, Li R, Lu T, Xiao G. Upregulation of microRNA-196a and microRNA-196b cooperatively correlate with aggressive progression and unfavorable prognosis in patients with colorectal cancer. Cancer Cell Int. 2014;14(1):128.
  • Raue R, Frank AC, Syed SN, Brüne B. Therapeutic Targeting of MicroRNAs in the Tumor Microenvironment. Int J Mol Sci. 2021;22(4):2210.
  • Huang X, Zhu X, Yu Y, et al. Dissecting miRNA signature in colorectal cancer progression and metastasis. Cancer Lett. 2021;501:66-82.
  • Kulkarni B, Kirave P, Gondaliya P, et al. Exosomal miRNA in chemoresistance, immune evasion, metastasis and progression of cancer. Drug Discov Today. 2019;24(10):2058-2067.
There are 16 citations in total.

Details

Primary Language English
Subjects Surgery (Other)
Journal Section Research Articles
Authors

Bahar Canbay Torun 0000-0002-6353-6692

Şakir Ümit Zeybek 0000-0001-8403-2939

Türker Bulut 0000-0003-3311-3581

Yılmaz Büyükuncu 0000-0003-2477-8848

Emel Canbay 0000-0001-7592-3000

Publication Date October 27, 2024
Submission Date October 6, 2024
Acceptance Date October 17, 2024
Published in Issue Year 2024 Volume: 7 Issue: 3

Cite

AMA Canbay Torun B, Zeybek ŞÜ, Bulut T, Büyükuncu Y, Canbay E. The Relationship Between miR-196a2 Polymorphism and Colorectal Cancer Risk. Acta Med Nicomedia. October 2024;7(3):348-352. doi:10.53446/actamednicomedia.1562372

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