Let-7a microRNA suppresses therapeutics-induced cancer cell death by targeting caspase-3
MicroRNAs (miRNA) are endogenously expressed non-coding RNAs that regulate gene expression post-transcriptionally. Let-7a miRNA is a founding member in the let-7 family and its down-regulation in association with over-expression of RAS and HMGA2 oncogenes has previously been reported. In the present...
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description | MicroRNAs (miRNA) are endogenously expressed non-coding RNAs that regulate gene expression post-transcriptionally. Let-7a miRNA is a founding member in the let-7 family and its down-regulation in association with over-expression of RAS and HMGA2 oncogenes has previously been reported. In the present study, caspase-3, the executioner caspase, was confirmed to be the target of let-7a as ectopic expression of let-7a decreased the luciferase activity of a reporter construct containing the 3' untranslated region of caspase-3 and at the same time repressed the enzyme expression in human squamous carcinoma A431 cells and hepatocellular carcinoma HepG2 cells. Moreover, let-7a was over-expressed while caspase-3 was down-regulated in A10A cells, a doxorubicin-resistant A431 subline. Enforced let-7a expression increased the resistance in A431 cells and HepG2 cells to apoptosis induced by therapeutic drugs such as interferon-gamma, doxorubicin and paclitaxel. On the other hand, down-regulation of let-7a by the anti-let-7a inhibitor increased the doxorubicin-induced apoptosis in A431 parent cells, A10A cells and HepG2 cells while the increase was suppressed by caspase-3 inhibitor. Both anti-let-7a inhibitor and caspase-3 inhibitor however failed to affect the drug-induced apoptosis in human breast cancer MCF7 cells, the cells that do not express caspase-3. Therefore, let-7a by targeting caspase-3 may play a functional role in modulating drug-induced cell death in human cancer cells. |
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Let-7a miRNA is a founding member in the let-7 family and its down-regulation in association with over-expression of RAS and HMGA2 oncogenes has previously been reported. In the present study, caspase-3, the executioner caspase, was confirmed to be the target of let-7a as ectopic expression of let-7a decreased the luciferase activity of a reporter construct containing the 3' untranslated region of caspase-3 and at the same time repressed the enzyme expression in human squamous carcinoma A431 cells and hepatocellular carcinoma HepG2 cells. Moreover, let-7a was over-expressed while caspase-3 was down-regulated in A10A cells, a doxorubicin-resistant A431 subline. Enforced let-7a expression increased the resistance in A431 cells and HepG2 cells to apoptosis induced by therapeutic drugs such as interferon-gamma, doxorubicin and paclitaxel. On the other hand, down-regulation of let-7a by the anti-let-7a inhibitor increased the doxorubicin-induced apoptosis in A431 parent cells, A10A cells and HepG2 cells while the increase was suppressed by caspase-3 inhibitor. Both anti-let-7a inhibitor and caspase-3 inhibitor however failed to affect the drug-induced apoptosis in human breast cancer MCF7 cells, the cells that do not express caspase-3. Therefore, let-7a by targeting caspase-3 may play a functional role in modulating drug-induced cell death in human cancer cells.</description><identifier>ISSN: 1360-8185</identifier><identifier>EISSN: 1573-675X</identifier><identifier>DOI: 10.1007/s10495-008-0256-z</identifier><identifier>PMID: 18758960</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Antineoplastic Agents - pharmacology ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Caspase 3 - genetics ; Caspase 3 - metabolism ; Cell Biology ; Cell death ; Cell Death - drug effects ; Cell Line, Tumor ; Doxorubicin - pharmacology ; Drug Screening Assays, Antitumor ; Gene Expression Regulation, Neoplastic - drug effects ; Humans ; Interferon-gamma - pharmacology ; MicroRNAs - chemistry ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Neoplasms - drug therapy ; Neoplasms - enzymology ; Neoplasms - genetics ; Neoplasms - pathology ; Nucleic Acid Conformation ; Oncology ; Original Paper ; Paclitaxel - pharmacology ; Reproducibility of Results ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Virology</subject><ispartof>Apoptosis (London), 2008-10, Vol.13 (10), p.1215-1222</ispartof><rights>Springer Science+Business Media, LLC 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-198f12c54334950cf6e0921265a75f979e72984def94d10689d0581c3d267fd83</citedby><cites>FETCH-LOGICAL-c393t-198f12c54334950cf6e0921265a75f979e72984def94d10689d0581c3d267fd83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10495-008-0256-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10495-008-0256-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18758960$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsang, Wing Pui</creatorcontrib><creatorcontrib>Kwok, Tim Tak</creatorcontrib><title>Let-7a microRNA suppresses therapeutics-induced cancer cell death by targeting caspase-3</title><title>Apoptosis (London)</title><addtitle>Apoptosis</addtitle><addtitle>Apoptosis</addtitle><description>MicroRNAs (miRNA) are endogenously expressed non-coding RNAs that regulate gene expression post-transcriptionally. Let-7a miRNA is a founding member in the let-7 family and its down-regulation in association with over-expression of RAS and HMGA2 oncogenes has previously been reported. In the present study, caspase-3, the executioner caspase, was confirmed to be the target of let-7a as ectopic expression of let-7a decreased the luciferase activity of a reporter construct containing the 3' untranslated region of caspase-3 and at the same time repressed the enzyme expression in human squamous carcinoma A431 cells and hepatocellular carcinoma HepG2 cells. Moreover, let-7a was over-expressed while caspase-3 was down-regulated in A10A cells, a doxorubicin-resistant A431 subline. Enforced let-7a expression increased the resistance in A431 cells and HepG2 cells to apoptosis induced by therapeutic drugs such as interferon-gamma, doxorubicin and paclitaxel. On the other hand, down-regulation of let-7a by the anti-let-7a inhibitor increased the doxorubicin-induced apoptosis in A431 parent cells, A10A cells and HepG2 cells while the increase was suppressed by caspase-3 inhibitor. Both anti-let-7a inhibitor and caspase-3 inhibitor however failed to affect the drug-induced apoptosis in human breast cancer MCF7 cells, the cells that do not express caspase-3. Therefore, let-7a by targeting caspase-3 may play a functional role in modulating drug-induced cell death in human cancer cells.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Caspase 3 - genetics</subject><subject>Caspase 3 - metabolism</subject><subject>Cell Biology</subject><subject>Cell death</subject><subject>Cell Death - drug effects</subject><subject>Cell Line, Tumor</subject><subject>Doxorubicin - pharmacology</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Humans</subject><subject>Interferon-gamma - pharmacology</subject><subject>MicroRNAs - chemistry</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - enzymology</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - pathology</subject><subject>Nucleic Acid Conformation</subject><subject>Oncology</subject><subject>Original Paper</subject><subject>Paclitaxel - pharmacology</subject><subject>Reproducibility of Results</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Virology</subject><issn>1360-8185</issn><issn>1573-675X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kE1rFTEUhoMo9kN_gBsdXHQXPUkmX8tS_IKLglroLqTJmdsp986MOTOL9teby1wouHCVwHneNycPY28EfBAA9iMJaL3mAI6D1IY_PmOnQlvFjdU3z-tdGeBOOH3CzojuAUA51b5kJ8JZ7byBU3azwZnb2Oz7VMaf3y8bWqapIBFSM99hiRMuc5-I90NeEuYmxSFhaRLudk3GON81tw_NHMsW537Y1jFNkZCrV-xFF3eEr4_nObv-_On31Ve--fHl29Xlhifl1cyFd52QSbdK1a9A6gyCl0IaHa3uvPVopXdtxs63WYBxPoN2Iqksje2yU-fsYu2dyvhnQZrDvqfDdnHAcaFgvG6FbXUF3_8D3o9LGepuQSojtDFgKyRWqNogKtiFqfT7WB6CgHBwHlbnoToPB-fhsWbeHouX2z3mp8RRcgXkClAdDVssTy__r_XdGuriGOK29BSuf0kQCoRuwUql_gKM05Rl</recordid><startdate>20081001</startdate><enddate>20081001</enddate><creator>Tsang, Wing Pui</creator><creator>Kwok, Tim Tak</creator><general>Boston : Springer US</general><general>Springer US</general><general>Springer Nature B.V</general><scope>FBQ</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>7QP</scope><scope>7RQ</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</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>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>20081001</creationdate><title>Let-7a microRNA suppresses therapeutics-induced cancer cell death by targeting caspase-3</title><author>Tsang, Wing Pui ; Kwok, Tim Tak</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-198f12c54334950cf6e0921265a75f979e72984def94d10689d0581c3d267fd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Antineoplastic Agents - 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Academic</collection><jtitle>Apoptosis (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsang, Wing Pui</au><au>Kwok, Tim Tak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Let-7a microRNA suppresses therapeutics-induced cancer cell death by targeting caspase-3</atitle><jtitle>Apoptosis (London)</jtitle><stitle>Apoptosis</stitle><addtitle>Apoptosis</addtitle><date>2008-10-01</date><risdate>2008</risdate><volume>13</volume><issue>10</issue><spage>1215</spage><epage>1222</epage><pages>1215-1222</pages><issn>1360-8185</issn><eissn>1573-675X</eissn><abstract>MicroRNAs (miRNA) are endogenously expressed non-coding RNAs that regulate gene expression post-transcriptionally. Let-7a miRNA is a founding member in the let-7 family and its down-regulation in association with over-expression of RAS and HMGA2 oncogenes has previously been reported. In the present study, caspase-3, the executioner caspase, was confirmed to be the target of let-7a as ectopic expression of let-7a decreased the luciferase activity of a reporter construct containing the 3' untranslated region of caspase-3 and at the same time repressed the enzyme expression in human squamous carcinoma A431 cells and hepatocellular carcinoma HepG2 cells. Moreover, let-7a was over-expressed while caspase-3 was down-regulated in A10A cells, a doxorubicin-resistant A431 subline. Enforced let-7a expression increased the resistance in A431 cells and HepG2 cells to apoptosis induced by therapeutic drugs such as interferon-gamma, doxorubicin and paclitaxel. On the other hand, down-regulation of let-7a by the anti-let-7a inhibitor increased the doxorubicin-induced apoptosis in A431 parent cells, A10A cells and HepG2 cells while the increase was suppressed by caspase-3 inhibitor. Both anti-let-7a inhibitor and caspase-3 inhibitor however failed to affect the drug-induced apoptosis in human breast cancer MCF7 cells, the cells that do not express caspase-3. Therefore, let-7a by targeting caspase-3 may play a functional role in modulating drug-induced cell death in human cancer cells.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>18758960</pmid><doi>10.1007/s10495-008-0256-z</doi><tpages>8</tpages></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Biochemistry Biomedical and Life Sciences Biomedicine Cancer Research Caspase 3 - genetics Caspase 3 - metabolism Cell Biology Cell death Cell Death - drug effects Cell Line, Tumor Doxorubicin - pharmacology Drug Screening Assays, Antitumor Gene Expression Regulation, Neoplastic - drug effects Humans Interferon-gamma - pharmacology MicroRNAs - chemistry MicroRNAs - genetics MicroRNAs - metabolism Neoplasms - drug therapy Neoplasms - enzymology Neoplasms - genetics Neoplasms - pathology Nucleic Acid Conformation Oncology Original Paper Paclitaxel - pharmacology Reproducibility of Results RNA, Messenger - genetics RNA, Messenger - metabolism Virology |
title | Let-7a microRNA suppresses therapeutics-induced cancer cell death by targeting caspase-3 |
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