Functional mechanism and clinical implications of miR-141 in human cancers
Cancer is caused by the abnormal proliferation of local tissue cells under the control of many oncogenic factors. MicroRNAs (miRNAs) are a class of evolutionarily conserved, approximately 22-nucleotide noncoding small RNAs that influence transcriptional regulationby binding to the 3′-untranslated re...
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Veröffentlicht in: | Cellular signalling 2022-07, Vol.95, p.110354-110354, Article 110354 |
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creator | Luo, Qi-qi Tian, Yu Qu, Guang-jin Kun-Huang Luo, Shan-shun |
description | Cancer is caused by the abnormal proliferation of local tissue cells under the control of many oncogenic factors. MicroRNAs (miRNAs) are a class of evolutionarily conserved, approximately 22-nucleotide noncoding small RNAs that influence transcriptional regulationby binding to the 3′-untranslated region of target messenger RNA. As a member of the miRNA family, miR-141 acts as a suppressor or an oncomiR in various cancers and regulates cancer cell proliferation, apoptosis, invasion, and metastasis through a variety of signaling pathways, such as phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT) and constitutive activation of nuclear factor-κB (NF-κB). Target gene validation and pathway analysis have provided mechanistic insight into the role of this miRNA in different tissues. This review also outlines novel findings that suggest miR-141 may be useful as a noninvasive biomarker and as a therapeutic target in several cancers.
•Regulatory mechanisms of miR-141 in cancer•Regulatory roles of miR-141 in various cancers•miR-141 as a tumor drug therapy•miR-141 as a drug resistance•miR-141 as a diagnostic marker of cancers |
doi_str_mv | 10.1016/j.cellsig.2022.110354 |
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•Regulatory mechanisms of miR-141 in cancer•Regulatory roles of miR-141 in various cancers•miR-141 as a tumor drug therapy•miR-141 as a drug resistance•miR-141 as a diagnostic marker of cancers</description><subject>cancer</subject><subject>Diagnosis</subject><subject>Mechanisms</subject><subject>miR-141</subject><subject>Signal pathways</subject><subject>Therapeutic</subject><issn>0898-6568</issn><issn>1873-3913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMo7rr6E5QevbTOJE22PYksrh8sCKLnkKapm6VN16QV_Pe2dPXqaYbheWeYh5BLhAQBxc0u0aaug_1IKFCaIALj6RGZY7ZkMcuRHZM5ZHkWCy6yGTkLYQeAHAQ9JTPGOQdc0jl5XvdOd7Z1qo4ao7fK2dBEypWRrq2zehjbZl8PzQiFqK2ixr7GmGJkXbTtG-UirZw2PpyTk0rVwVwc6oK8r-_fVo_x5uXhaXW3iTUTvItLpFQoKAudUgFgONCMVgVUhqNmaV6UXHNghWApV3muaAqojaGqEJUusGALcj3t3fv2szehk40NowzlTNsHSYVIlzlmyAeUT6j2bQjeVHLvbaP8t0SQo0a5kweNctQoJ41D7upwoi8aU_6lfr0NwO0EmOHRL2u8DNqaQUNpvdGdLFv7z4kffR-FNw</recordid><startdate>202207</startdate><enddate>202207</enddate><creator>Luo, Qi-qi</creator><creator>Tian, Yu</creator><creator>Qu, Guang-jin</creator><creator>Kun-Huang</creator><creator>Luo, Shan-shun</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202207</creationdate><title>Functional mechanism and clinical implications of miR-141 in human cancers</title><author>Luo, Qi-qi ; Tian, Yu ; Qu, Guang-jin ; Kun-Huang ; Luo, Shan-shun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-d1226a0dbc42600e50282fb0fe51c349bd5c503b6345a99a2401cee2ab6fcb1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>cancer</topic><topic>Diagnosis</topic><topic>Mechanisms</topic><topic>miR-141</topic><topic>Signal pathways</topic><topic>Therapeutic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Qi-qi</creatorcontrib><creatorcontrib>Tian, Yu</creatorcontrib><creatorcontrib>Qu, Guang-jin</creatorcontrib><creatorcontrib>Kun-Huang</creatorcontrib><creatorcontrib>Luo, Shan-shun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular signalling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Qi-qi</au><au>Tian, Yu</au><au>Qu, Guang-jin</au><au>Kun-Huang</au><au>Luo, Shan-shun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional mechanism and clinical implications of miR-141 in human cancers</atitle><jtitle>Cellular signalling</jtitle><addtitle>Cell Signal</addtitle><date>2022-07</date><risdate>2022</risdate><volume>95</volume><spage>110354</spage><epage>110354</epage><pages>110354-110354</pages><artnum>110354</artnum><issn>0898-6568</issn><eissn>1873-3913</eissn><abstract>Cancer is caused by the abnormal proliferation of local tissue cells under the control of many oncogenic factors. MicroRNAs (miRNAs) are a class of evolutionarily conserved, approximately 22-nucleotide noncoding small RNAs that influence transcriptional regulationby binding to the 3′-untranslated region of target messenger RNA. As a member of the miRNA family, miR-141 acts as a suppressor or an oncomiR in various cancers and regulates cancer cell proliferation, apoptosis, invasion, and metastasis through a variety of signaling pathways, such as phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT) and constitutive activation of nuclear factor-κB (NF-κB). Target gene validation and pathway analysis have provided mechanistic insight into the role of this miRNA in different tissues. This review also outlines novel findings that suggest miR-141 may be useful as a noninvasive biomarker and as a therapeutic target in several cancers.
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subjects | cancer Diagnosis Mechanisms miR-141 Signal pathways Therapeutic |
title | Functional mechanism and clinical implications of miR-141 in human cancers |
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