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Long non‐coding RNA ADAMTS9‐AS1 inhibits the progression of prostate cancer by modulating the miR‐142‐5p/CCND1 axis
Background Emerging evidence has implied the importance of long non‐coding RNAs in cancer development, including prostate cancer (PCa). Bioinformatic analyses have identified that ADAMTS9‐AS1 may play a role in cancer progression. Methods A quantitative real‐time polymerase chain reaction was conduc...
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Published in: | The journal of gene medicine 2021-05, Vol.23 (5), p.e3331-n/a |
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container_title | The journal of gene medicine |
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creator | Zhou, Zhien Wu, Xingcheng Zhou, Yi Yan, Weigang |
description | Background
Emerging evidence has implied the importance of long non‐coding RNAs in cancer development, including prostate cancer (PCa). Bioinformatic analyses have identified that ADAMTS9‐AS1 may play a role in cancer progression.
Methods
A quantitative real‐time polymerase chain reaction was conducted to measure ADAMTS9‐AS1 expression level at messenger RNA level. In vitro functional analyses were performed to investigate cell behaviors status under different conditions. Moreover, rescue assays were conducted to explore the potential mechanisms of ADAMTS9‐AS1 in PCa progression.
Results
ADAMTS9‐AS1 expression is down‐regulated in PCa. Forcing ADAMTS9‐AS1 expression impedes PCa cell proliferation via initiating cell apoptosis. Importantly, microRNA‐142‐5p (miR‐142‐5p) mimic and small‐interfering RNA targeting cyclin D1 (CCND1, si‐CCND1) could attenuate the inhibitory effects of ADAMTS9‐AS1 overexpression on PCa cell growth.
Conclusions
Collectively, our results indicate that ADAMTS9‐AS1 suppresses PCa progression by regulating the miR‐142‐5p/CCND1 axis, which provides a new mechanism for the progression of PCa.
ADAMTS9‐AS1 serves as a tumor suppressor in prostate cancer by regulating the miR‐142‐5p/CCND1 axis. |
doi_str_mv | 10.1002/jgm.3331 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2500375415</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2520681329</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3491-1c135fb4a634a8a1c688f71ed5693703c36bc86be540c8961f9694ef99e3ab483</originalsourceid><addsrcrecordid>eNp1kdFO2zAUhi20iQKbxBNMlnazm1Cf2E7sy6gdBdQyCZi0u8hxndZVEpc4EVTc8Ag8I0-CM9iQJu3G9jn6_Okc_QgdAzkBQuLxZlWfUEphDx0AjyGKY84-hDeRMmJS_BqhQ-83hEAqhNxHI0pTwkQqD9DD3DUr3Ljm-fFJu6UNxdVlhrNptri5lqGZXQO2zdoWtvO4Wxu8bd2qNd5b12BXDqXvVGewVo02LS52uHbLvlLd4Bo-1PYqeIDF4eTb8WRyOQWs7q3_hD6WqvLm89t9hH6efr-ZnEXzH7PzSTaPNGUSItBAeVkwlVCmhAKdCFGmYJY8kWEPqmlSaJEUhjOihUyglIlkppTSUFUwQY_Qt1dvmPW2N77La-u1qSrVGNf7POaE0JQz4AH9-g-6cX3bhOkCFZNEAI3lu1CH5X1rynzb2lq1uxxIPgSSh0DyIZCAfnkT9kVtln_BPwkEIHoF7mxldv8V5RezxW_hC1TKlR8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2520681329</pqid></control><display><type>article</type><title>Long non‐coding RNA ADAMTS9‐AS1 inhibits the progression of prostate cancer by modulating the miR‐142‐5p/CCND1 axis</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Zhou, Zhien ; Wu, Xingcheng ; Zhou, Yi ; Yan, Weigang</creator><creatorcontrib>Zhou, Zhien ; Wu, Xingcheng ; Zhou, Yi ; Yan, Weigang</creatorcontrib><description>Background
Emerging evidence has implied the importance of long non‐coding RNAs in cancer development, including prostate cancer (PCa). Bioinformatic analyses have identified that ADAMTS9‐AS1 may play a role in cancer progression.
Methods
A quantitative real‐time polymerase chain reaction was conducted to measure ADAMTS9‐AS1 expression level at messenger RNA level. In vitro functional analyses were performed to investigate cell behaviors status under different conditions. Moreover, rescue assays were conducted to explore the potential mechanisms of ADAMTS9‐AS1 in PCa progression.
Results
ADAMTS9‐AS1 expression is down‐regulated in PCa. Forcing ADAMTS9‐AS1 expression impedes PCa cell proliferation via initiating cell apoptosis. Importantly, microRNA‐142‐5p (miR‐142‐5p) mimic and small‐interfering RNA targeting cyclin D1 (CCND1, si‐CCND1) could attenuate the inhibitory effects of ADAMTS9‐AS1 overexpression on PCa cell growth.
Conclusions
Collectively, our results indicate that ADAMTS9‐AS1 suppresses PCa progression by regulating the miR‐142‐5p/CCND1 axis, which provides a new mechanism for the progression of PCa.
ADAMTS9‐AS1 serves as a tumor suppressor in prostate cancer by regulating the miR‐142‐5p/CCND1 axis.</description><identifier>ISSN: 1099-498X</identifier><identifier>EISSN: 1521-2254</identifier><identifier>DOI: 10.1002/jgm.3331</identifier><identifier>PMID: 33704879</identifier><language>eng</language><publisher>England: Wiley Periodicals Inc</publisher><subject>ADAMTS9‐AS1 ; Apoptosis ; Apoptosis - genetics ; CCND1 ; Cell growth ; Cell Line, Tumor ; Cell Movement - genetics ; Cell proliferation ; Cell Proliferation - genetics ; Cyclin D1 ; Cyclin D1 - genetics ; Disease Progression ; Gene expression ; Gene Expression Regulation, Neoplastic ; Gene therapy ; Humans ; long non‐coding RNA ; Male ; MicroRNAs - genetics ; miRNA ; miR‐142‐5p ; Non-coding RNA ; Polymerase chain reaction ; Prostate cancer ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - pathology ; RNA, Long Noncoding - genetics ; Signal Transduction - genetics</subject><ispartof>The journal of gene medicine, 2021-05, Vol.23 (5), p.e3331-n/a</ispartof><rights>2021 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3491-1c135fb4a634a8a1c688f71ed5693703c36bc86be540c8961f9694ef99e3ab483</citedby><cites>FETCH-LOGICAL-c3491-1c135fb4a634a8a1c688f71ed5693703c36bc86be540c8961f9694ef99e3ab483</cites><orcidid>0000-0002-5704-4157</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33704879$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Zhien</creatorcontrib><creatorcontrib>Wu, Xingcheng</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Yan, Weigang</creatorcontrib><title>Long non‐coding RNA ADAMTS9‐AS1 inhibits the progression of prostate cancer by modulating the miR‐142‐5p/CCND1 axis</title><title>The journal of gene medicine</title><addtitle>J Gene Med</addtitle><description>Background
Emerging evidence has implied the importance of long non‐coding RNAs in cancer development, including prostate cancer (PCa). Bioinformatic analyses have identified that ADAMTS9‐AS1 may play a role in cancer progression.
Methods
A quantitative real‐time polymerase chain reaction was conducted to measure ADAMTS9‐AS1 expression level at messenger RNA level. In vitro functional analyses were performed to investigate cell behaviors status under different conditions. Moreover, rescue assays were conducted to explore the potential mechanisms of ADAMTS9‐AS1 in PCa progression.
Results
ADAMTS9‐AS1 expression is down‐regulated in PCa. Forcing ADAMTS9‐AS1 expression impedes PCa cell proliferation via initiating cell apoptosis. Importantly, microRNA‐142‐5p (miR‐142‐5p) mimic and small‐interfering RNA targeting cyclin D1 (CCND1, si‐CCND1) could attenuate the inhibitory effects of ADAMTS9‐AS1 overexpression on PCa cell growth.
Conclusions
Collectively, our results indicate that ADAMTS9‐AS1 suppresses PCa progression by regulating the miR‐142‐5p/CCND1 axis, which provides a new mechanism for the progression of PCa.
ADAMTS9‐AS1 serves as a tumor suppressor in prostate cancer by regulating the miR‐142‐5p/CCND1 axis.</description><subject>ADAMTS9‐AS1</subject><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>CCND1</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - genetics</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - genetics</subject><subject>Cyclin D1</subject><subject>Cyclin D1 - genetics</subject><subject>Disease Progression</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gene therapy</subject><subject>Humans</subject><subject>long non‐coding RNA</subject><subject>Male</subject><subject>MicroRNAs - genetics</subject><subject>miRNA</subject><subject>miR‐142‐5p</subject><subject>Non-coding RNA</subject><subject>Polymerase chain reaction</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - pathology</subject><subject>RNA, Long Noncoding - genetics</subject><subject>Signal Transduction - genetics</subject><issn>1099-498X</issn><issn>1521-2254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kdFO2zAUhi20iQKbxBNMlnazm1Cf2E7sy6gdBdQyCZi0u8hxndZVEpc4EVTc8Ag8I0-CM9iQJu3G9jn6_Okc_QgdAzkBQuLxZlWfUEphDx0AjyGKY84-hDeRMmJS_BqhQ-83hEAqhNxHI0pTwkQqD9DD3DUr3Ljm-fFJu6UNxdVlhrNptri5lqGZXQO2zdoWtvO4Wxu8bd2qNd5b12BXDqXvVGewVo02LS52uHbLvlLd4Bo-1PYqeIDF4eTb8WRyOQWs7q3_hD6WqvLm89t9hH6efr-ZnEXzH7PzSTaPNGUSItBAeVkwlVCmhAKdCFGmYJY8kWEPqmlSaJEUhjOihUyglIlkppTSUFUwQY_Qt1dvmPW2N77La-u1qSrVGNf7POaE0JQz4AH9-g-6cX3bhOkCFZNEAI3lu1CH5X1rynzb2lq1uxxIPgSSh0DyIZCAfnkT9kVtln_BPwkEIHoF7mxldv8V5RezxW_hC1TKlR8</recordid><startdate>202105</startdate><enddate>202105</enddate><creator>Zhou, Zhien</creator><creator>Wu, Xingcheng</creator><creator>Zhou, Yi</creator><creator>Yan, Weigang</creator><general>Wiley Periodicals Inc</general><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>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5704-4157</orcidid></search><sort><creationdate>202105</creationdate><title>Long non‐coding RNA ADAMTS9‐AS1 inhibits the progression of prostate cancer by modulating the miR‐142‐5p/CCND1 axis</title><author>Zhou, Zhien ; Wu, Xingcheng ; Zhou, Yi ; Yan, Weigang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3491-1c135fb4a634a8a1c688f71ed5693703c36bc86be540c8961f9694ef99e3ab483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>ADAMTS9‐AS1</topic><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>CCND1</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - genetics</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - genetics</topic><topic>Cyclin D1</topic><topic>Cyclin D1 - genetics</topic><topic>Disease Progression</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gene therapy</topic><topic>Humans</topic><topic>long non‐coding RNA</topic><topic>Male</topic><topic>MicroRNAs - genetics</topic><topic>miRNA</topic><topic>miR‐142‐5p</topic><topic>Non-coding RNA</topic><topic>Polymerase chain reaction</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - pathology</topic><topic>RNA, Long Noncoding - genetics</topic><topic>Signal Transduction - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Zhien</creatorcontrib><creatorcontrib>Wu, Xingcheng</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Yan, Weigang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of gene medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Zhien</au><au>Wu, Xingcheng</au><au>Zhou, Yi</au><au>Yan, Weigang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long non‐coding RNA ADAMTS9‐AS1 inhibits the progression of prostate cancer by modulating the miR‐142‐5p/CCND1 axis</atitle><jtitle>The journal of gene medicine</jtitle><addtitle>J Gene Med</addtitle><date>2021-05</date><risdate>2021</risdate><volume>23</volume><issue>5</issue><spage>e3331</spage><epage>n/a</epage><pages>e3331-n/a</pages><issn>1099-498X</issn><eissn>1521-2254</eissn><abstract>Background
Emerging evidence has implied the importance of long non‐coding RNAs in cancer development, including prostate cancer (PCa). Bioinformatic analyses have identified that ADAMTS9‐AS1 may play a role in cancer progression.
Methods
A quantitative real‐time polymerase chain reaction was conducted to measure ADAMTS9‐AS1 expression level at messenger RNA level. In vitro functional analyses were performed to investigate cell behaviors status under different conditions. Moreover, rescue assays were conducted to explore the potential mechanisms of ADAMTS9‐AS1 in PCa progression.
Results
ADAMTS9‐AS1 expression is down‐regulated in PCa. Forcing ADAMTS9‐AS1 expression impedes PCa cell proliferation via initiating cell apoptosis. Importantly, microRNA‐142‐5p (miR‐142‐5p) mimic and small‐interfering RNA targeting cyclin D1 (CCND1, si‐CCND1) could attenuate the inhibitory effects of ADAMTS9‐AS1 overexpression on PCa cell growth.
Conclusions
Collectively, our results indicate that ADAMTS9‐AS1 suppresses PCa progression by regulating the miR‐142‐5p/CCND1 axis, which provides a new mechanism for the progression of PCa.
ADAMTS9‐AS1 serves as a tumor suppressor in prostate cancer by regulating the miR‐142‐5p/CCND1 axis.</abstract><cop>England</cop><pub>Wiley Periodicals Inc</pub><pmid>33704879</pmid><doi>10.1002/jgm.3331</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5704-4157</orcidid></addata></record> |
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subjects | ADAMTS9‐AS1 Apoptosis Apoptosis - genetics CCND1 Cell growth Cell Line, Tumor Cell Movement - genetics Cell proliferation Cell Proliferation - genetics Cyclin D1 Cyclin D1 - genetics Disease Progression Gene expression Gene Expression Regulation, Neoplastic Gene therapy Humans long non‐coding RNA Male MicroRNAs - genetics miRNA miR‐142‐5p Non-coding RNA Polymerase chain reaction Prostate cancer Prostatic Neoplasms - genetics Prostatic Neoplasms - pathology RNA, Long Noncoding - genetics Signal Transduction - genetics |
title | Long non‐coding RNA ADAMTS9‐AS1 inhibits the progression of prostate cancer by modulating the miR‐142‐5p/CCND1 axis |
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