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Hepatocellular carcinoma (HCC) is sexually dimorphic in mammals. Forkhead box A2 (FOXA2) binding sites' mutations exhibited impairment in binding between FOXA2, hormonal receptors and their target genes. Some miRNA genes were found to be located in cancer-associated genomic regions, indicating that they are cancer-related and could be used as prognostic and diagnostic biomarkers as well as potential molecular targets. Molecular mechanism underlying sexual dimorphism remains unclear. This study aimed to investigate FOXA2 DNA binding domain (DBD) polymorphism and miRNA-124 expression profile to correlate its differential expression to HCC in view of sexual dimorphism in Egyptian patients.
A propos de l'auteur
Miss Nourhan Y. Mostafa was born in 1990 and was graduated from Biotechnology Program, Faculty of Science, Cairo University in 2011. In 2012, she worked as Research Assistant in NRC, Egypt. In 2013, she was appointed as a Demonstrator in Biotechnology Program. She received her M.Sc in Biotechnology from Faculty of Science, Cairo University in 2016.
