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• W3196600511 abstract "Abstract Purpose We aimed to identify the epithelial-mesenchymal transition and associated putative targets of the miR-34 family in transcriptomic data of cervical epithelial squamous cell carcinoma (CESC) to find new therapeutic targets for better disease management. Methods A combined computational analysis of the miR-34 family; gene expression in heterogeneous primary CESCs derived from TCGA; and the integration of miR-34b and EMT-regulated genes was performed. Four EMT-associated miR-34b gene targets were analysed in primary human CESC and non-cancerous cervical tissues by qRT-PCR. Effects of endogenous miR-34b expression and its associated gene modulations in cervical cancer cells (C33A and HeLa) were analysed using qRT-PCR, western blotting and immunofluorescence, transwell migration and invasion assays. Results The results showed that the miR-34 family might regulate the mTOR pathway, cell cycle ( CCND2 ) and cell adhesion functions ( FZD4 ). Further, we showed that a low negative correlation (r 2 = −0.07) between miR-34b/EMĨ score and four EMT signature genes ( E>MP7, CAV1, ID2, FN1 ) were significantly regulated by miR-34b . Also, FN1 was indicated as its putative target with the highest negative EMT score and high binding energy between MRE/3’UTR. Further, these transcriptomic signatures in CESC revealed a significant inverse correlation across the stages of primary human CESC. These genes were repressed at transcriptional and translational levels in miR-34b-3p expressing C33A and HeLa cells, contributing to their reduced cell migration and invasive properties. Conclusions Our studies revealed the potential targets of the miR-34 family, especially miR-34b , that can emerge as potential biomarkers and promising therapeutic targets in CESC disease management." @default.
• W3196600511 created "2021-09-13" @default.
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• W3196600511 date "2021-09-03" @default.
• W3196600511 modified "2023-09-25" @default.
• W3196600511 title "<i>miR-34b</i>associates with epithelial-mesenchymal transition and regulates<i>BMP7, CAV1, ID2</i>and<i>FN1</i>in human cervical cancer" @default.
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• W3196600511 doi "https://doi.org/10.1101/2021.09.02.458804" @default.
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