Therapeutic Use of MicroRNAs in Lung Cancer
Lung cancer is a leading cause of cancer deaths worldwide. Although the molecular pathways of lung cancer have been partly known, the high mortality rate is not markedly changed. MicroRNAs (miRNAs) are small noncoding RNAs that actively modulate cell physiological processes as apoptosis, cell-cycle...
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description | Lung cancer is a leading cause of cancer deaths worldwide. Although the molecular pathways of lung cancer have been partly known, the high mortality rate is not markedly changed. MicroRNAs (miRNAs) are small noncoding RNAs that actively modulate cell physiological processes as apoptosis, cell-cycle control, cell proliferation, DNA repair, and metabolism. Several studies demonstrated that miRNAs are involved in the pathogenesis of lung diseases including lung cancer and they negatively regulate gene and protein expression by acting as oncogenes or tumor suppressors. In this review we summarize the current knowledge on the role of miRNAs and their target genes in lung tumorigenesis and evaluate their potential use as therapeutic agents in lung cancer. In particular, we describe methodological approaches such as inhibition of oncogenic miRNAs or replacement of tumor suppressor miRNAs, both in in vitro and in vivo assays. Furthermore we discuss new strategies to achieve in vivo tissue specific delivery, potential off-target effects, and safety of miRNAs systemic delivery. |
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Although the molecular pathways of lung cancer have been partly known, the high mortality rate is not markedly changed. MicroRNAs (miRNAs) are small noncoding RNAs that actively modulate cell physiological processes as apoptosis, cell-cycle control, cell proliferation, DNA repair, and metabolism. Several studies demonstrated that miRNAs are involved in the pathogenesis of lung diseases including lung cancer and they negatively regulate gene and protein expression by acting as oncogenes or tumor suppressors. In this review we summarize the current knowledge on the role of miRNAs and their target genes in lung tumorigenesis and evaluate their potential use as therapeutic agents in lung cancer. In particular, we describe methodological approaches such as inhibition of oncogenic miRNAs or replacement of tumor suppressor miRNAs, both in in vitro and in vivo assays. Furthermore we discuss new strategies to achieve in vivo tissue specific delivery, potential off-target effects, and safety of miRNAs systemic delivery.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2014/756975</identifier><identifier>PMID: 25309923</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animals ; Biomedical research ; Cancer ; Cancer therapies ; Carcinogenesis - genetics ; Carcinogenesis - pathology ; Care and treatment ; Drug Delivery Systems ; Gene therapy ; Genetic aspects ; Genomics ; Health aspects ; Humans ; Kinases ; Lung cancer ; Lung Neoplasms - drug therapy ; Lung Neoplasms - genetics ; Medical prognosis ; Medical research ; MicroRNA ; MicroRNAs ; MicroRNAs - therapeutic use ; Mortality ; Mutation ; Review ; Risk assessment ; Rodents ; Tumors</subject><ispartof>BioMed research international, 2014-01, Vol.2014 (2014), p.1-8</ispartof><rights>Copyright © 2014 Orazio Fortunato et al.</rights><rights>COPYRIGHT 2014 John Wiley & Sons, Inc.</rights><rights>Copyright © 2014 Orazio Fortunato et al. Orazio Fortunato et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2014 Orazio Fortunato et al. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-df73637128ce019ba4a446fb16f6173dac7729f3ceed08b3b0b405a46ae324453</citedby><cites>FETCH-LOGICAL-c528t-df73637128ce019ba4a446fb16f6173dac7729f3ceed08b3b0b405a46ae324453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182304/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182304/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25309923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Gandellini, Paolo</contributor><creatorcontrib>Moro, Massimo</creatorcontrib><creatorcontrib>Verri, Carla</creatorcontrib><creatorcontrib>Boeri, Mattia</creatorcontrib><creatorcontrib>Fortunato, Orazio</creatorcontrib><creatorcontrib>Sozzi, Gabriella</creatorcontrib><title>Therapeutic Use of MicroRNAs in Lung Cancer</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Lung cancer is a leading cause of cancer deaths worldwide. Although the molecular pathways of lung cancer have been partly known, the high mortality rate is not markedly changed. MicroRNAs (miRNAs) are small noncoding RNAs that actively modulate cell physiological processes as apoptosis, cell-cycle control, cell proliferation, DNA repair, and metabolism. Several studies demonstrated that miRNAs are involved in the pathogenesis of lung diseases including lung cancer and they negatively regulate gene and protein expression by acting as oncogenes or tumor suppressors. In this review we summarize the current knowledge on the role of miRNAs and their target genes in lung tumorigenesis and evaluate their potential use as therapeutic agents in lung cancer. In particular, we describe methodological approaches such as inhibition of oncogenic miRNAs or replacement of tumor suppressor miRNAs, both in in vitro and in vivo assays. Furthermore we discuss new strategies to achieve in vivo tissue specific delivery, potential off-target effects, and safety of miRNAs systemic delivery.</description><subject>Animals</subject><subject>Biomedical research</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Carcinogenesis - genetics</subject><subject>Carcinogenesis - pathology</subject><subject>Care and treatment</subject><subject>Drug Delivery Systems</subject><subject>Gene therapy</subject><subject>Genetic aspects</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Kinases</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - therapeutic use</subject><subject>Mortality</subject><subject>Mutation</subject><subject>Review</subject><subject>Risk assessment</subject><subject>Rodents</subject><subject>Tumors</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkU1rGzEQhkVpaUKaU-9hIZfS4Eajz91LwZgkLbgNhOQstNqRrbDWupI3Jf8-Mk7ctKfOZQR6eKSZl5CPQL8ASHnOKIhzLVWj5RtyyDiIiQIBb_dnzg_Icc73tFQNijbqPTlgktOmYfyQnN0uMdk1jpvgqruM1eCrH8Gl4ebnNFchVvMxLqqZjQ7TB_LO2z7j8XM_IneXF7ezb5P59dX32XQ-cZLVm0nnNVdcA6sdUmhaK6wQyregvALNO-u0Zo3nDrGjdctb2goqrVAWORNC8iPydeddj-0KO4dxk2xv1imsbHo0gw3m75sYlmYxPBgBNeNUFMGnZ0Eafo2YN2YVssO-txGHMRtQUIOsSxX09B_0fhhTLOMZkErRWnAt_1AL26MJ0Q_lXbeVmqlgmjLBpSrU2Y4q68s5od9_GajZpmW2aZldWoU-eT3lnn3JpgCfd8AyxM7-Dv9nw4Kgt69gUFJQ_gRSfKIJ</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Moro, Massimo</creator><creator>Verri, Carla</creator><creator>Boeri, Mattia</creator><creator>Fortunato, Orazio</creator><creator>Sozzi, Gabriella</creator><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7TM</scope><scope>5PM</scope></search><sort><creationdate>20140101</creationdate><title>Therapeutic Use of MicroRNAs in Lung Cancer</title><author>Moro, Massimo ; Verri, Carla ; Boeri, Mattia ; Fortunato, Orazio ; Sozzi, Gabriella</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-df73637128ce019ba4a446fb16f6173dac7729f3ceed08b3b0b405a46ae324453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Biomedical research</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Carcinogenesis - 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Although the molecular pathways of lung cancer have been partly known, the high mortality rate is not markedly changed. MicroRNAs (miRNAs) are small noncoding RNAs that actively modulate cell physiological processes as apoptosis, cell-cycle control, cell proliferation, DNA repair, and metabolism. Several studies demonstrated that miRNAs are involved in the pathogenesis of lung diseases including lung cancer and they negatively regulate gene and protein expression by acting as oncogenes or tumor suppressors. In this review we summarize the current knowledge on the role of miRNAs and their target genes in lung tumorigenesis and evaluate their potential use as therapeutic agents in lung cancer. In particular, we describe methodological approaches such as inhibition of oncogenic miRNAs or replacement of tumor suppressor miRNAs, both in in vitro and in vivo assays. Furthermore we discuss new strategies to achieve in vivo tissue specific delivery, potential off-target effects, and safety of miRNAs systemic delivery.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>25309923</pmid><doi>10.1155/2014/756975</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomedical research Cancer Cancer therapies Carcinogenesis - genetics Carcinogenesis - pathology Care and treatment Drug Delivery Systems Gene therapy Genetic aspects Genomics Health aspects Humans Kinases Lung cancer Lung Neoplasms - drug therapy Lung Neoplasms - genetics Medical prognosis Medical research MicroRNA MicroRNAs MicroRNAs - therapeutic use Mortality Mutation Review Risk assessment Rodents Tumors |
title | Therapeutic Use of MicroRNAs in Lung Cancer |
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