Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET

The tumor microenvironment (TEM) comprise of various cellular and molecular components such as fibroblasts, immune cells, bone marrow-derived inflammatory cells, endothelial cells, extracellular matrix (ECM), and signaling molecules. The complex crosstalk between (TEM) components and malignant cells...

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Main Authors: Razak, Eliza, Yusof, Faridah, Ahmad Raus, Raha
Format: Proceeding Paper
Language:English
Published: Kulliyyah of Engineering, International Islamic University Malaysia 2016
Subjects:
Online Access:http://irep.iium.edu.my/51251/
http://irep.iium.edu.my/51251/1/51251_Ectopic_miRNA_network.pdf
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author Razak, Eliza
Yusof, Faridah
Ahmad Raus, Raha
author_facet Razak, Eliza
Yusof, Faridah
Ahmad Raus, Raha
author_sort Razak, Eliza
building IIUM Repository
collection Online Access
description The tumor microenvironment (TEM) comprise of various cellular and molecular components such as fibroblasts, immune cells, bone marrow-derived inflammatory cells, endothelial cells, extracellular matrix (ECM), and signaling molecules. The complex crosstalk between (TEM) components and malignant cells can give rise to tumorigenesis, progression, and angiogenesis as well as micro-metastasis and macro-metastasis. MicroRNAs (miRNAs) are small, non-coding extracellular RNAs involved in post-transcriptional regulation of gene silencing or degradation by base paring at open reading frame (ORF) region of the target mRNA. Recent advances in the miRNA field have driven to the understanding of multiple regulatory aspects concerning cancer biology. Aberrant miRNA expression in malignant tumors compared with normal tissue are promising biomarkers for cancer diagnosis. Epithelial-to-mesenchymal transition (EMT) is a reversible process in which neoplastic epithelial cells expressed mesenchymal phenotypes and resulting in alteration of cell autonomous mechanisms. EMT enables epithelial cells to lose their cell polarity, acquire cancer stem cell-like properties which favor tumor invasion, extravasation and metastasis. Mesenchymal–epithelial transition (MET) is the inverse process of EMT. This results in stabilization of distant metastases by permitting cancerous cells to recoup epithelial phenotypes and integrate into distant organs. Ectopic microRNA expression and disturbed signaling pathways have been associated with EMT and MET processes. This review describes the co-regulatory loops among miRNAs, target genes and important regulatory pathways involved in cancer.
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format Proceeding Paper
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institution International Islamic University Malaysia
institution_category Local University
language English
last_indexed 2025-11-14T16:27:22Z
publishDate 2016
publisher Kulliyyah of Engineering, International Islamic University Malaysia
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spelling iium-512512017-01-13T08:24:05Z http://irep.iium.edu.my/51251/ Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET Razak, Eliza Yusof, Faridah Ahmad Raus, Raha TP248.13 Biotechnology The tumor microenvironment (TEM) comprise of various cellular and molecular components such as fibroblasts, immune cells, bone marrow-derived inflammatory cells, endothelial cells, extracellular matrix (ECM), and signaling molecules. The complex crosstalk between (TEM) components and malignant cells can give rise to tumorigenesis, progression, and angiogenesis as well as micro-metastasis and macro-metastasis. MicroRNAs (miRNAs) are small, non-coding extracellular RNAs involved in post-transcriptional regulation of gene silencing or degradation by base paring at open reading frame (ORF) region of the target mRNA. Recent advances in the miRNA field have driven to the understanding of multiple regulatory aspects concerning cancer biology. Aberrant miRNA expression in malignant tumors compared with normal tissue are promising biomarkers for cancer diagnosis. Epithelial-to-mesenchymal transition (EMT) is a reversible process in which neoplastic epithelial cells expressed mesenchymal phenotypes and resulting in alteration of cell autonomous mechanisms. EMT enables epithelial cells to lose their cell polarity, acquire cancer stem cell-like properties which favor tumor invasion, extravasation and metastasis. Mesenchymal–epithelial transition (MET) is the inverse process of EMT. This results in stabilization of distant metastases by permitting cancerous cells to recoup epithelial phenotypes and integrate into distant organs. Ectopic microRNA expression and disturbed signaling pathways have been associated with EMT and MET processes. This review describes the co-regulatory loops among miRNAs, target genes and important regulatory pathways involved in cancer. Kulliyyah of Engineering, International Islamic University Malaysia 2016 Proceeding Paper PeerReviewed application/pdf en http://irep.iium.edu.my/51251/1/51251_Ectopic_miRNA_network.pdf Razak, Eliza and Yusof, Faridah and Ahmad Raus, Raha (2016) Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET. In: 4th International Conference on Biotechnology Engineering 2016 (ICBioE 2016), 25th-27th July 2016, Kuala Lumpur. http://iiumpress.iium.edu.my/bookshop/orthodontics-and-you
spellingShingle TP248.13 Biotechnology
Razak, Eliza
Yusof, Faridah
Ahmad Raus, Raha
Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET
title Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET
title_full Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET
title_fullStr Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET
title_full_unstemmed Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET
title_short Ectopic miRNA network and the crosstalk between different signalling pathways during EMT and MET
title_sort ectopic mirna network and the crosstalk between different signalling pathways during emt and met
topic TP248.13 Biotechnology
url http://irep.iium.edu.my/51251/
http://irep.iium.edu.my/51251/
http://irep.iium.edu.my/51251/1/51251_Ectopic_miRNA_network.pdf