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microRNA Expression in Ethnic Specific Early Stage Breast Cancer: an Integration and Comparative Analysis

Breast cancer (BC) has a higher incidence in young Lebanese woman as compared to the West. We assessed the microRNA (miRNA) microarray profile of tissues derived from Lebanese patients with early BC and performed mRNA-miRNA integration analysis. 173 miRNAs were significantly dysregulated in 45 BC ve...

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Detalles Bibliográficos
Autores principales: Nassar, Farah J., Talhouk, Rabih, Zgheib, Nathalie K., Tfayli, Arafat, El Sabban, Maya, El Saghir, Nagi S., Boulos, Fouad, Jabbour, Mark N., Chalala, Claude, Boustany, Rose-Mary, Kadara, Humam, Zhang, Zhou, Zheng, Yinan, Joyce, Brian, Hou, Lifang, Bazarbachi, Ali, Calin, George, Nasr, Rihab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715135/
https://www.ncbi.nlm.nih.gov/pubmed/29203780
http://dx.doi.org/10.1038/s41598-017-16978-y
Descripción
Sumario:Breast cancer (BC) has a higher incidence in young Lebanese woman as compared to the West. We assessed the microRNA (miRNA) microarray profile of tissues derived from Lebanese patients with early BC and performed mRNA-miRNA integration analysis. 173 miRNAs were significantly dysregulated in 45 BC versus 17 normal adjacent breast tissues, including 74 with a fold change more than two of which 17 were never reported before in cancer. Integration analysis of mRNA-miRNA microarray data revealed a potential role of 51 dysregulated miRNA regulating 719 tumor suppressive or oncogenic mRNA associated with increased proliferation and decreased migration and invasion. We then performed a comparative miRNA microarray profile analysis of BC tissue between these 45 Lebanese and 197 matched American BC patients. Notably, Lebanese BC patients had 21 exclusively dysregulated miRNA (e.g. miR-31, 362-3p, and 663) and 4 miRNA with different expression manner compared to American patients (e.g. miR-1288-star and 324-3p). Some of these differences could reflect variation in patient age at diagnosis or ethnic variation affecting miRNA epigenetic regulation or sequence of miRNA precursors. Our data provide a basis for genetic/epigenetic investigations to explore the role of miRNA in early stage BC in young women, including ethnic specific differences.