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Reciprocal effects between microRNA-140-5p and ADAM10 suppress migration and invasion of human tongue cancer cells
Authors:Yang Kai  Wang Peng  Wu Ling  Hao Jiebing  Bian Zhuan
Institution:1. State Key Laboratory Breeding Base of Basic Science of Stomatology and Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan 430079, China;2. The Second Charity Hospital of Henan Province, Jiaozuo 454000, China
Abstract:ADAM10, overexpressed in tongue squamous cell carcinoma (TSCC), has been well documented for its role in tumor progression and metastasis. In the present study, we evaluated the inhibition effect of microRNAs (miRNAs) on the TSCC and identified that miR-140-5p could directly targets ADAM10 and inhibits the invasion and migration of TSCC cells. LAMC1, HDAC7 and PAX6, clustered into migration-related genes, were validated to be direct targets of miR-140-5p, while IGF1R and PSEN1 were not responsible to the regulation. Most intriguingly, ERBB4 was upregulated by miR-140-5p even though the interaction between ERBB4 3′UTR and miR-140-5p existed simultaneously. Meanwhile, ADAM10 is involved in the “positive” regulation of ERBB4 and negative regulation of PAX6 by miR-140-5p. Taken together, our results suggest that miR-140-5p play a role in TSCC cell migration and invasion, and two brand new relationships between miRNA and its targets emerged: (1) ADAM10 is not just a direct target of miR-140-5p, the repressed ADAM10 also helps to enhance the effect of miR-140-5p to other target genes: ERBB4 and PAX6; (2) ERBB4 is “positively” regulated by miR-140-5p.
Keywords:ADAM10  A disintegrin and metalloproteinase 10  TSCC  tongue squamous cell carcinoma  miRNA  microRNA  UTR  untranslated region  WT  wild type  MUT  mutant  siADAM10  siRNAs against ADAM10  ERBB4  v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4
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