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ErbB4 3'-UTR Variant (c.*3622A>G) is Associated with ER/PR Negativity and Advanced Breast Cancer.
Tabatabian, Maryam; Mesrian Tanha, Hamzeh; Tabatabaeian, Hossein; Sadeghi, Samira; Ghaedi, Kamran; Mohamadynejad, Parisa.
Afiliación
  • Tabatabian M; Department of Biology, Faculty of Basic Science, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
  • Mesrian Tanha H; 2Cellular and Molecular Biology Division, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, 81746-73441 Iran.
  • Tabatabaeian H; 3Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
  • Sadeghi S; 4Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Ghaedi K; 3Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
  • Mohamadynejad P; 5Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Indian J Clin Biochem ; 35(1): 115-120, 2020 Jan.
Article en En | MEDLINE | ID: mdl-32071504
ABSTRACT
A genetic variant may alter a gene expression level and as a result be associated with pathological characteristics in breast cancer. In this research, the frequency and association of the ErbB4 3'-untranslated region (3'-UTR) variant, rs12471583 (c.*3622A>G) was studied in an Iranian breast cancer patients. In silico assessment was performed to predict the function of the rs12471583 variant located on the 3'-UTR of ErbB4. Furthermore, as a case-control study, this polymorphism was genotyped in 243 breast cancer patients and non-cancerous controls using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. The Armitage's trend test and regular association tests were performed to analyze a possible association between the rs12471583 and risk of breast cancer and its relevant pathological traits. The bioinformatics analysis predicted that the rs12471583 SNP is located on the four miRNA binding sites, including miR-511-5p, miR-4659a-5p, miR-4659b-5p, and miR-6830-3p. According to logistic regression tests, the G allele is negatively associated with ER- (OR = 0.20, 95% C.I. = 0.04-0.93, p = 0.026), PR- (OR = 0.31, 95% C.I. = 0.10-0.98, p = 0.039), ER-/PR- (OR = 0.20, 95% C.I. = 0.04-0.93, p = 0.026), and advanced breast cancer (OR = 0.40, 95% C.I. = 0.18-0.85, p = 0.016). It has been found that ErbB4 expression may be linked to unfavorable outcomes in breast cancer. Likewise, our results suggest that the G allele may strengthen miRNA-ErbB4 binding efficiency and as a result reduce expression of ErbB4. This is a possible explanation for the observed association.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Indian J Clin Biochem Año: 2020 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Indian J Clin Biochem Año: 2020 Tipo del documento: Article País de afiliación: Irán