Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8644527 | Gene | 2018 | 22 Pages |
Abstract
Epithelial to mesenchymal transition (EMT) is a phenomenon in which epithelial cells lose their cell to cell adhesion and detach from the base of the membrane. EMT is a fundamental process which occurs during tumor progression and metastasis. Cancer genomics is a complex network which involves a variety of factors such as transcription factors (TFs), coding genes and microRNAs (miRs). Both TFs and miRs are trans-regulatory elements that crosstalk. Due to a wide range of targets, TF-miR interaction provides a feedback or feedforward loop and cross-gene regulation consequently. In this review, we focused on the structure and function of two TF families involved in EMT, zinc finger and β helix loop helix and p53. Subsequently we analyzed recent findings on TF-miR interaction in EMT.
Keywords
BMP1EZH2LSD1SMADH3K4Wnt3aH3K9LEF1histone 3 lysine 9ZEBH3K27lymphoid enhancer binding factor 1E1A binding protein P300Suv39h1EP300SIN3ATGF-βKDM1Aenhancer of zeste 2 polycomb repressive complex 2 subunitH2A histone family member XCDH1MEF2GSCNPCbHLHGSK-3βZEB1PRCHDACBmi1Mdm2basic helix loop helixTransforming Growth Factor BetaEMTSnailmyocyte enhancer factor 2MetastasisMicroRNAMiRNAhistone 3 lysine 27Twistcadherin-1Nasopharyngeal carcinomaglycogen synthase kinase 3 beta
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Authors
Neda Alidadiani, Shahrooz Ghaderi, Nafi Dilaver, Saina Bakhshamin, Mansour Bayat,