Literature DB >> 33069925

Association study of IL10 gene polymorphisms (rs1800872 and rs1800896) with cervical cancer in the Bangladeshi women.

Anamika Datta1, Fatema Tuz Zahora1, Md Abdul Aziz1, Mohammad Sarowar Uddin1, Mahmuda Ferdous1, Md Shalahuddin Millat1, Md Shahid Sarwar1, Md Abdul Barek1, Sarah Jafrin1, Shamsun Nahar2, Mohammad Safiqul Islam3.   

Abstract

OBJECTIVE: Cervical cancer is one of the most destructive diseases among females worldwide, especially in developing countries. Interleukin-10 (IL10) is a multifunctional cytokine, and polymorphisms in the IL10 gene have been identified in multiple malignancies. However, no prior studies were conducted to determine the association of IL10 polymorphisms (rs1800872 and rs1800896) with cervical cancer patients in Bangladesh.
METHODS: This case-control study was carried out on 240 cervical cancer patients and 204 healthy volunteers. Genotyping was performed using the tetra-primer amplification refractory mutation system polymerase chain reaction (ARMS-PCR).
RESULTS: In the case of rs1800872, CA and AA genotypes significantly increased the risk of cervical cancer (OR = 1.59, 95% CI = 1.01-2.49, p = 0.043; OR = 2.75, 95% CI = 1.53-4.93, p = 0.0007, respectively) but the significance did not exist for CA genotype after Bonferroni correction (p < 0.025). An increased risk was also observed for the dominant model, recessive model, and allele model (A vs. C) of rs1800872 (dominant model: OR = 1.83, 95% CI = 1.18-2.80, p = 0.006; recessive model: OR = 2.00, 95% CI = 1.22-3.29, p = 0.006; allele model: OR = 1.55, 95% CI = 1.19-2.03, p = 0.001) which remained significant after the correction of Bonferroni. For rs1800896, only GG genotype and recessive model showed increased risk for cervical cancer (GG vs. AA: OR = 3.48, 95% CI = 1.46-8.31, p = 0.005; recessive model: OR = 3.57, 95% CI = 1.52-8.38, p = 0.003). These associations were statistically significant, and the significance existed after Bonferroni correction. Haplotype analysis revealed that AA haplotype significantly increased the risk (OR = 1.56, p = 0.001) whereas, CA haplotype significantly lowered the risk (OR = 0.42, p = 2.42x10-8), and both rs1800872 and rs1800896 are strongly in linkage disequilibrium (D'=1, r2 = 0.333). Moreover, the IL10 mRNA level was found up-regulated in silico in cervical squamous cell carcinoma tissues compared to healthy tissues (p = 1.11x10-16).
CONCLUSION: Our study suggests that rs1800872 and rs1800896 polymorphisms of IL10 gene are associated with cervical cancer in Bangladeshi females.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cervical cancer; Genetic polymorphism; IL10; Tetra-primer ARMS-PCR

Mesh:

Substances:

Year:  2020        PMID: 33069925     DOI: 10.1016/j.intimp.2020.107091

Source DB:  PubMed          Journal:  Int Immunopharmacol        ISSN: 1567-5769            Impact factor:   4.932


  2 in total

1.  CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case-control study combined with a meta-analysis.

Authors:  Mohammad Sarowar Uddin; Atkia Azima; Md Abdul Aziz; Tutun Das Aka; Sarah Jafrin; Md Shalahuddin Millat; Shafayet Ahmed Siddiqui; Md Giash Uddin; Md Saddam Hussain; Mohammad Safiqul Islam
Journal:  Hum Cell       Date:  2021-05-05       Impact factor: 4.174

Review 2.  Association of the Interleukin-10-592C/A Polymorphism and Cervical Cancer Risk: A Meta-Analysis.

Authors:  Brehima Diakite; Yaya Kassogue; Mamoudou Maiga; Guimogo Dolo; Oumar Kassogue; Jonah Musa; Imran Morhason-Bello; Ban Traore; Cheick Bougadari Traore; Bakarou Kamate; Aissata Coulibaly; Sekou Bah; Sellama Nadifi; Robert Murphy; Jane L Holl; Lifang Hou
Journal:  Genet Res (Camb)       Date:  2022-07-12       Impact factor: 1.375

  2 in total

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