Quantitative investigation of BRIP1 and PALB2 expression level in Iranian women with breast cancer compared to normal samples

Message:
Article Type:
Research/Original Article (دارای رتبه معتبر)
Abstract:
Background
Breast Cancer is the most common cancer in the world and it is the second reason of death between women following the lung cancer. The aim of this study was quantitative evaluation of BRIP1 and PALB2 genes expression level in blood samples of breast cancer comparing with normal people to investigate the role of these two genes as biomarkers during breast cancer diagnosis and screening.
Materials and methods
In this case- control study, we investigated the expression level of BRIP1 and PALB2 genes among 50 breast cancer patients in comparison with 50 control cases. Total RNA from blood samples were extracted and cDNA was synthesized. The specific primer for detection of gene markers was designed and expression level of BRIP1 and PALB2 in presence of GAPDH control gene was quantitatively studied by using qRT-PCR.
Results
The level of BRIP1 andPALB2 gene expression was significantly increased in breast cancer patients compared to control population. Results showed quantitative increase of BRIP1 and PALB2 genes with 3.419 and 7.326 fold respectively for breast cancer compared to normal samples (P=0.001). Also, the results were evaluated using the formulas 2-ΔΔCt according to the mean Ct of healthy subjects and grading of the disease showed a significant relationship with the expression of genes, so that by increasing staging and severity of cancer, the expression of biomarkers increased (p=0.003).
Conclusion
Based on significant increasing expression of PALB2 and BRIP1 genes in breast cancer patients in our study, probably increasing expression of these genes will inhibit the activity of tumor suppressor genes. So, we can introduce these genes as biomarker of breast cancer in the diagnostic work up of disease.
Language:
Persian
Published:
Medical Science Journal of Islamic Azad Univesity Tehran Medical Branch, Volume:28 Issue: 4, 2018
Pages:
283 to 289
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