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Long Noncoding RNA and Epithelial Mesenchymal Transition in Cancer
Epithelial-mesenchymal transition (EMT) is a multistep process that allows epithelial cells to acquire mesenchymal properties. Fundamental in the early stages of embryonic development, this process is aberrantly activated in aggressive cancerous cells to gain motility and invasion capacity, thus pro...
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Published in: | International journal of molecular sciences 2019-04, Vol.20 (8), p.1924 |
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description | Epithelial-mesenchymal transition (EMT) is a multistep process that allows epithelial cells to acquire mesenchymal properties. Fundamental in the early stages of embryonic development, this process is aberrantly activated in aggressive cancerous cells to gain motility and invasion capacity, thus promoting metastatic phenotypes. For this reason, EMT is a central topic in cancer research and its regulation by a plethora of mechanisms has been reported. Recently, genomic sequencing and functional genomic studies deepened our knowledge on the fundamental regulatory role of noncoding DNA. A large part of the genome is transcribed in an impressive number of noncoding RNAs. Among these, long noncoding RNAs (lncRNAs) have been reported to control several biological processes affecting gene expression at multiple levels from transcription to protein localization and stability. Up to now, more than 8000 lncRNAs were discovered as selectively expressed in cancer cells. Their elevated number and high expression specificity candidate these molecules as a valuable source of biomarkers and potential therapeutic targets. Rising evidence currently highlights a relevant function of lncRNAs on EMT regulation defining a new layer of involvement of these molecules in cancer biology. In this review we aim to summarize the findings on the role of lncRNAs on EMT regulation and to discuss their prospective potential value as biomarkers and therapeutic targets in cancer. |
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Fundamental in the early stages of embryonic development, this process is aberrantly activated in aggressive cancerous cells to gain motility and invasion capacity, thus promoting metastatic phenotypes. For this reason, EMT is a central topic in cancer research and its regulation by a plethora of mechanisms has been reported. Recently, genomic sequencing and functional genomic studies deepened our knowledge on the fundamental regulatory role of noncoding DNA. A large part of the genome is transcribed in an impressive number of noncoding RNAs. Among these, long noncoding RNAs (lncRNAs) have been reported to control several biological processes affecting gene expression at multiple levels from transcription to protein localization and stability. Up to now, more than 8000 lncRNAs were discovered as selectively expressed in cancer cells. Their elevated number and high expression specificity candidate these molecules as a valuable source of biomarkers and potential therapeutic targets. Rising evidence currently highlights a relevant function of lncRNAs on EMT regulation defining a new layer of involvement of these molecules in cancer biology. In this review we aim to summarize the findings on the role of lncRNAs on EMT regulation and to discuss their prospective potential value as biomarkers and therapeutic targets in cancer.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20081924</identifier><identifier>PMID: 31003545</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>1-Phosphatidylinositol 3-kinase ; Annotations ; Antisense RNA ; Cancer ; Cell adhesion & migration ; Cell cycle ; Cell growth ; Deoxyribonucleic acid ; DNA ; Enhancers ; Epigenetics ; Epithelial to Mesenchymal Transition (EMT) ; Gene expression ; Growth factors ; Intracellular signalling ; Kinases ; long noncoding RNAs (lncRNAs) ; MAP kinase ; Mesenchyme ; Metastasis ; Peptides ; Post-translation ; Protein kinase ; Proteins ; Regulatory sequences ; Review ; RNA polymerase ; RNA-binding protein ; Transcription factors ; Tumorigenesis ; Tumors ; Wnt protein</subject><ispartof>International journal of molecular sciences, 2019-04, Vol.20 (8), p.1924</ispartof><rights>2019. 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Fundamental in the early stages of embryonic development, this process is aberrantly activated in aggressive cancerous cells to gain motility and invasion capacity, thus promoting metastatic phenotypes. For this reason, EMT is a central topic in cancer research and its regulation by a plethora of mechanisms has been reported. Recently, genomic sequencing and functional genomic studies deepened our knowledge on the fundamental regulatory role of noncoding DNA. A large part of the genome is transcribed in an impressive number of noncoding RNAs. Among these, long noncoding RNAs (lncRNAs) have been reported to control several biological processes affecting gene expression at multiple levels from transcription to protein localization and stability. Up to now, more than 8000 lncRNAs were discovered as selectively expressed in cancer cells. Their elevated number and high expression specificity candidate these molecules as a valuable source of biomarkers and potential therapeutic targets. 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In this review we aim to summarize the findings on the role of lncRNAs on EMT regulation and to discuss their prospective potential value as biomarkers and therapeutic targets in cancer.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>Annotations</subject><subject>Antisense RNA</subject><subject>Cancer</subject><subject>Cell adhesion & migration</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Enhancers</subject><subject>Epigenetics</subject><subject>Epithelial to Mesenchymal Transition (EMT)</subject><subject>Gene expression</subject><subject>Growth factors</subject><subject>Intracellular signalling</subject><subject>Kinases</subject><subject>long noncoding RNAs (lncRNAs)</subject><subject>MAP kinase</subject><subject>Mesenchyme</subject><subject>Metastasis</subject><subject>Peptides</subject><subject>Post-translation</subject><subject>Protein kinase</subject><subject>Proteins</subject><subject>Regulatory sequences</subject><subject>Review</subject><subject>RNA polymerase</subject><subject>RNA-binding protein</subject><subject>Transcription factors</subject><subject>Tumorigenesis</subject><subject>Tumors</subject><subject>Wnt protein</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkc9rFDEUx4MotlZvnmXAiwe3vvzcyUVol2oL2wpSz-FNktnNMpOsyazQ_960W8tWCOSRfPjkvXwJeU_hlHMNX8JmLAygpZqJF-SYCsZmAGr-8qA-Im9K2QAwzqR-TY44BeBSyGNyvkxx1dykaJMLtfp5c9ZgdM3FNkxrPwQcmmtffLTru7HWtxljCVNIsQmxWWC0Pr8lr3ocin_3uJ-QX98ubheXs-WP71eLs-XMSiGmmXfC9cgECMoFgkTJVO1bO21lTzWoDizTHW0RHXTKzq3vUfdet1J3qp_zE3K197qEG7PNYcR8ZxIG83CQ8spgnoIdvNHKKkspVS3Xos5Zn2DCK9X1IBy2vLq-7l3bXTd6Z32cMg7PpM9vYlibVfpjlKRSMl0Fnx4FOf3e-TKZMRTrhwGjT7tiGKNUC6GlqujH_9BN2uVYv8owzuvimt5Tn_eUzamU7PunZiiY-6DNYdAV_3A4wBP8L1n-F_jhokU</recordid><startdate>20190418</startdate><enddate>20190418</enddate><creator>Gugnoni, Mila</creator><creator>Ciarrocchi, Alessia</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-4630-3958</orcidid><orcidid>https://orcid.org/0000-0002-5541-2075</orcidid></search><sort><creationdate>20190418</creationdate><title>Long Noncoding RNA and Epithelial Mesenchymal Transition in Cancer</title><author>Gugnoni, Mila ; Ciarrocchi, Alessia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c544t-ed4dfa2404134a05a5262009d9c5f1906b0c29b18aad0b6c7cefa9fe9859b6f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>Annotations</topic><topic>Antisense RNA</topic><topic>Cancer</topic><topic>Cell adhesion & migration</topic><topic>Cell cycle</topic><topic>Cell growth</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Enhancers</topic><topic>Epigenetics</topic><topic>Epithelial to Mesenchymal Transition (EMT)</topic><topic>Gene expression</topic><topic>Growth factors</topic><topic>Intracellular signalling</topic><topic>Kinases</topic><topic>long noncoding RNAs (lncRNAs)</topic><topic>MAP kinase</topic><topic>Mesenchyme</topic><topic>Metastasis</topic><topic>Peptides</topic><topic>Post-translation</topic><topic>Protein kinase</topic><topic>Proteins</topic><topic>Regulatory sequences</topic><topic>Review</topic><topic>RNA polymerase</topic><topic>RNA-binding protein</topic><topic>Transcription factors</topic><topic>Tumorigenesis</topic><topic>Tumors</topic><topic>Wnt protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gugnoni, Mila</creatorcontrib><creatorcontrib>Ciarrocchi, Alessia</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gugnoni, Mila</au><au>Ciarrocchi, Alessia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long Noncoding RNA and Epithelial Mesenchymal Transition in Cancer</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2019-04-18</date><risdate>2019</risdate><volume>20</volume><issue>8</issue><spage>1924</spage><pages>1924-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Epithelial-mesenchymal transition (EMT) is a multistep process that allows epithelial cells to acquire mesenchymal properties. 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Rising evidence currently highlights a relevant function of lncRNAs on EMT regulation defining a new layer of involvement of these molecules in cancer biology. In this review we aim to summarize the findings on the role of lncRNAs on EMT regulation and to discuss their prospective potential value as biomarkers and therapeutic targets in cancer.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31003545</pmid><doi>10.3390/ijms20081924</doi><orcidid>https://orcid.org/0000-0003-4630-3958</orcidid><orcidid>https://orcid.org/0000-0002-5541-2075</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 1-Phosphatidylinositol 3-kinase Annotations Antisense RNA Cancer Cell adhesion & migration Cell cycle Cell growth Deoxyribonucleic acid DNA Enhancers Epigenetics Epithelial to Mesenchymal Transition (EMT) Gene expression Growth factors Intracellular signalling Kinases long noncoding RNAs (lncRNAs) MAP kinase Mesenchyme Metastasis Peptides Post-translation Protein kinase Proteins Regulatory sequences Review RNA polymerase RNA-binding protein Transcription factors Tumorigenesis Tumors Wnt protein |
title | Long Noncoding RNA and Epithelial Mesenchymal Transition in Cancer |
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