Potential value of circulatory microRNA10b gene expression and its target E‐cadherin as a prognostic and metastatic prediction marker for breast cancer
Autor: | Salwa Hamdi Gomaa, Fatma I. Dwedar, Ayman Farouk Mohammed, Reham Said Shams-Eldin, Salwa Nayer Mohamed |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Microbiology (medical)
Oncology Adult medicine.medical_specialty Clinical Biochemistry Breast Neoplasms Sensitivity and Specificity Metastasis Breast cancer breast cancer Downregulation and upregulation Antigens CD Internal medicine soluble E‐cadherin Gene expression microRNA TaqMan Biomarkers Tumor Immunology and Allergy Medicine circulating miR‐10b Humans Circulating MicroRNA Receptors Immunologic Research Articles Aged Membrane Glycoproteins Cadherin business.industry Biochemistry (medical) Public Health Environmental and Occupational Health TaqMan miRNA assay Hematology Middle Aged medicine.disease Cadherins Prognosis Gene Expression Regulation Neoplastic Medical Laboratory Technology non‐invasive biomarker ROC Curve Case-Control Studies Circulatory system Female business Research Article |
Zdroj: | Journal of Clinical Laboratory Analysis |
ISSN: | 1098-2825 0887-8013 |
Popis: | Background Breast cancer (BC) is the leading cause of cancer death in women worldwide. Most BC studies on candidate microRNAs were tissue specimen based. Recently, there has been a focus on the study of cell‐free circulating miRNAs as promising biomarkers in (BC) diagnosis and prognosis. Therefore, we aimed to investigate the circulating levels of miR‐10b and its target soluble E‐ cadherin as potentially easily accessible biomarkers for breast cancer. Methods Sixty‐one breast cancer patients and forty‐eight age‐ and sex‐matched healthy volunteers serving as a control group were enrolled in the present study. Serum samples were used to assess miRNA10b expression by TaqMan miRNA assay technique. In addition, soluble E‐cadherin expression level in serum was determined using ELISA technique. Result Circulating miR‐10b expression level and serum sE‐cadherin was significantly upregulated in patients with BC compared to controls. Moreover, serum miR‐10b displayed progressive up‐regulation in advanced stages with higher level in metastatic compared to non‐metastatic BC. Additionally, the combined use of both serum miR‐10b and sE‐cadherin revealed the highest sensitivity and specificity for detection of BC metastasis (92.9% and 97.9% respectively) with an area under curve (AUC) of 0.98, 95% CI (0.958–1.00). Conclusion Our data suggest that circulating miR‐10b could be utilized as a potential non‐invasive serum biomarker for diagnosis and prognosis of breast cancer with better performance to predict BC metastasis achieved on measuring it simultaneously with serum sE‐cadherin. Further studies with a large cohort of patients are warranted to validate the serum biomarker for breast cancer management. Our results emphasize the oncogenic role of miR‐10b and indicate that its high serum expression may be correlated with poor outcome in breast cancer. We suggest that miR‐10b has the potential to be used as non‐invasive breast cancer biomarker for diagnosis and prognosis and could be a novel tool in breast cancer management. Furthermore, circulating miR‐10b could help in the detection of breast cancer metastasis with better performance achieved on measuring it simultaneously with serum sE‐cadherin. Although, further studies with a large cohort of patients are warranted. |
Databáze: | OpenAIRE |
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