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GRASLND regulates melanoma cell progression by targeting the miR-218-5p/STAM2 axis
Increasing evidence suggests that long noncoding RNAs (lncRNAs) play important regulatory roles in biological processes and are dysregulated in numerous tumors. The lncRNA GRASLND functions as an oncogene in many cancers, but its role in skin cutaneous melanoma (SKCM) requires further investigation....
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Published in: | Journal of translational medicine 2024-07, Vol.22 (1), p.684-12, Article 684 |
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container_title | Journal of translational medicine |
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creator | Ma, Aiwei Shi, Wenqi Chen, Liyun Huang, Zijian Zhang, Yiwen Tang, Zixuan Jiang, Wenshi Xu, Mengjing Zhou, Jianda Zhang, Wancong Tang, Shijie |
description | Increasing evidence suggests that long noncoding RNAs (lncRNAs) play important regulatory roles in biological processes and are dysregulated in numerous tumors. The lncRNA GRASLND functions as an oncogene in many cancers, but its role in skin cutaneous melanoma (SKCM) requires further investigation.
SiRNA transfection, wound - healing and transwell assays were performed to evaluate the effect of GRASLND on cellular function.
The present study demonstrated that GRASLND expression is increased in SKCM tissues and cell lines. The high expression of GRASLND was correlated with poor prognosis and immunotherapy outcomes. Knockdown of GRASLND significantly inhibited cell migration and invasion. In addition, we found that miR-218-5p directly binds to its binding site on GRASLND, and GRASLND and miR-218-5p demonstrate mutual inhibition. Furthermore, the miR-218-5p inhibitor partially eliminated the knockdown of GRASLND and inhibited its expression. We also demonstrated that GRASLND acts as a miR-218-5p sponge that positively regulates STAM2 expression in SKCM cells.
In summary, these data suggest that GRASLND functions by regulating miR-218-5p/STAM2 expression, suggesting an important role for the lncRNA‒miRNA-mRNA functional network and a new potential therapeutic target for SKCM. |
doi_str_mv | 10.1186/s12967-024-05397-z |
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SiRNA transfection, wound - healing and transwell assays were performed to evaluate the effect of GRASLND on cellular function.
The present study demonstrated that GRASLND expression is increased in SKCM tissues and cell lines. The high expression of GRASLND was correlated with poor prognosis and immunotherapy outcomes. Knockdown of GRASLND significantly inhibited cell migration and invasion. In addition, we found that miR-218-5p directly binds to its binding site on GRASLND, and GRASLND and miR-218-5p demonstrate mutual inhibition. Furthermore, the miR-218-5p inhibitor partially eliminated the knockdown of GRASLND and inhibited its expression. We also demonstrated that GRASLND acts as a miR-218-5p sponge that positively regulates STAM2 expression in SKCM cells.
In summary, these data suggest that GRASLND functions by regulating miR-218-5p/STAM2 expression, suggesting an important role for the lncRNA‒miRNA-mRNA functional network and a new potential therapeutic target for SKCM.</description><identifier>ISSN: 1479-5876</identifier><identifier>EISSN: 1479-5876</identifier><identifier>DOI: 10.1186/s12967-024-05397-z</identifier><identifier>PMID: 39060946</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Base Sequence ; Biological markers ; Biomarker ; Care and treatment ; Cell Line, Tumor ; Cell Movement - genetics ; Cell Proliferation - genetics ; Development and progression ; Disease Progression ; Female ; Gene Expression Regulation, Neoplastic ; Gene Knockdown Techniques ; Genetic aspects ; Humans ; Immunotherapy ; lncRNA ; Male ; Melanoma ; Melanoma - genetics ; Melanoma - metabolism ; Melanoma - pathology ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Middle Aged ; Neoplasm Invasiveness ; Patient outcomes ; Prognosis ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; SKCM ; Skin Neoplasms - genetics ; Skin Neoplasms - metabolism ; Skin Neoplasms - pathology</subject><ispartof>Journal of translational medicine, 2024-07, Vol.22 (1), p.684-12, Article 684</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c361t-84647c6435574c1e1c3da1968c4c7916de3cddbd85f4db935ec785d5bc57ab603</cites><orcidid>0000-0002-5413-8828</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924,37012</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39060946$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Aiwei</creatorcontrib><creatorcontrib>Shi, Wenqi</creatorcontrib><creatorcontrib>Chen, Liyun</creatorcontrib><creatorcontrib>Huang, Zijian</creatorcontrib><creatorcontrib>Zhang, Yiwen</creatorcontrib><creatorcontrib>Tang, Zixuan</creatorcontrib><creatorcontrib>Jiang, Wenshi</creatorcontrib><creatorcontrib>Xu, Mengjing</creatorcontrib><creatorcontrib>Zhou, Jianda</creatorcontrib><creatorcontrib>Zhang, Wancong</creatorcontrib><creatorcontrib>Tang, Shijie</creatorcontrib><title>GRASLND regulates melanoma cell progression by targeting the miR-218-5p/STAM2 axis</title><title>Journal of translational medicine</title><addtitle>J Transl Med</addtitle><description>Increasing evidence suggests that long noncoding RNAs (lncRNAs) play important regulatory roles in biological processes and are dysregulated in numerous tumors. The lncRNA GRASLND functions as an oncogene in many cancers, but its role in skin cutaneous melanoma (SKCM) requires further investigation.
SiRNA transfection, wound - healing and transwell assays were performed to evaluate the effect of GRASLND on cellular function.
The present study demonstrated that GRASLND expression is increased in SKCM tissues and cell lines. The high expression of GRASLND was correlated with poor prognosis and immunotherapy outcomes. Knockdown of GRASLND significantly inhibited cell migration and invasion. In addition, we found that miR-218-5p directly binds to its binding site on GRASLND, and GRASLND and miR-218-5p demonstrate mutual inhibition. Furthermore, the miR-218-5p inhibitor partially eliminated the knockdown of GRASLND and inhibited its expression. We also demonstrated that GRASLND acts as a miR-218-5p sponge that positively regulates STAM2 expression in SKCM cells.
In summary, these data suggest that GRASLND functions by regulating miR-218-5p/STAM2 expression, suggesting an important role for the lncRNA‒miRNA-mRNA functional network and a new potential therapeutic target for SKCM.</description><subject>Analysis</subject><subject>Base Sequence</subject><subject>Biological markers</subject><subject>Biomarker</subject><subject>Care and treatment</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - genetics</subject><subject>Cell Proliferation - genetics</subject><subject>Development and progression</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gene Knockdown Techniques</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>lncRNA</subject><subject>Male</subject><subject>Melanoma</subject><subject>Melanoma - genetics</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - pathology</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Patient outcomes</subject><subject>Prognosis</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>SKCM</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - metabolism</subject><subject>Skin Neoplasms - pathology</subject><issn>1479-5876</issn><issn>1479-5876</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptkU9rFTEUxQex2Fr9Ai5kwI2btMnk__LRai28tvBa1yGT3BlTZibPZB7YfnrzOrUoyF3kcjnnRw6nqj4QfEKIEqeZNFpIhBuGMKdaosdX1RFhUiOupHj9135Yvc35HhclZ_pNdUg1FlgzcVRtLjar2_X1eZ2g3w12hlyPMNgpjrZ2MAz1NsU-Qc4hTnX7UM829TCHqa_nH1CPYYMaohDfnt7era6a2v4K-V110Nkhw_vn97j6_vXL3dk3tL65uDxbrZGjgsxIMcGkE4xyLpkjQBz1lmihHHNSE-GBOu9br3jHfKspBycV97x1XNpWYHpcXS5cH-292aYw2vRgog3m6RBTb2yagxvA6A48uMLRSjHfMSUlxZZ6aDSXHLPC-rywStyfO8izGUPe57cTxF02FCtOCNdSFemnRdrbQg5TF-dk3V5uVgo3UrCG74En_1GV8TAGFyfoQrn_Y2gWg0sx5wTdSyKCzb5us9RtSonmqW7zWEwfn7-9a0fwL5Y__dLfG-WiZg</recordid><startdate>20240726</startdate><enddate>20240726</enddate><creator>Ma, Aiwei</creator><creator>Shi, Wenqi</creator><creator>Chen, Liyun</creator><creator>Huang, Zijian</creator><creator>Zhang, Yiwen</creator><creator>Tang, Zixuan</creator><creator>Jiang, Wenshi</creator><creator>Xu, Mengjing</creator><creator>Zhou, Jianda</creator><creator>Zhang, Wancong</creator><creator>Tang, Shijie</creator><general>BioMed Central Ltd</general><general>BMC</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>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5413-8828</orcidid></search><sort><creationdate>20240726</creationdate><title>GRASLND regulates melanoma cell progression by targeting the miR-218-5p/STAM2 axis</title><author>Ma, Aiwei ; Shi, Wenqi ; Chen, Liyun ; Huang, Zijian ; Zhang, Yiwen ; Tang, Zixuan ; Jiang, Wenshi ; Xu, Mengjing ; Zhou, Jianda ; Zhang, Wancong ; Tang, Shijie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c361t-84647c6435574c1e1c3da1968c4c7916de3cddbd85f4db935ec785d5bc57ab603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Analysis</topic><topic>Base Sequence</topic><topic>Biological markers</topic><topic>Biomarker</topic><topic>Care and treatment</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - genetics</topic><topic>Cell Proliferation - genetics</topic><topic>Development and progression</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gene Knockdown Techniques</topic><topic>Genetic aspects</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>lncRNA</topic><topic>Male</topic><topic>Melanoma</topic><topic>Melanoma - genetics</topic><topic>Melanoma - metabolism</topic><topic>Melanoma - pathology</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Patient outcomes</topic><topic>Prognosis</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>SKCM</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - metabolism</topic><topic>Skin Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Aiwei</creatorcontrib><creatorcontrib>Shi, Wenqi</creatorcontrib><creatorcontrib>Chen, Liyun</creatorcontrib><creatorcontrib>Huang, Zijian</creatorcontrib><creatorcontrib>Zhang, Yiwen</creatorcontrib><creatorcontrib>Tang, Zixuan</creatorcontrib><creatorcontrib>Jiang, Wenshi</creatorcontrib><creatorcontrib>Xu, Mengjing</creatorcontrib><creatorcontrib>Zhou, Jianda</creatorcontrib><creatorcontrib>Zhang, Wancong</creatorcontrib><creatorcontrib>Tang, Shijie</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of translational medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Aiwei</au><au>Shi, Wenqi</au><au>Chen, Liyun</au><au>Huang, Zijian</au><au>Zhang, Yiwen</au><au>Tang, Zixuan</au><au>Jiang, Wenshi</au><au>Xu, Mengjing</au><au>Zhou, Jianda</au><au>Zhang, Wancong</au><au>Tang, Shijie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GRASLND regulates melanoma cell progression by targeting the miR-218-5p/STAM2 axis</atitle><jtitle>Journal of translational medicine</jtitle><addtitle>J Transl Med</addtitle><date>2024-07-26</date><risdate>2024</risdate><volume>22</volume><issue>1</issue><spage>684</spage><epage>12</epage><pages>684-12</pages><artnum>684</artnum><issn>1479-5876</issn><eissn>1479-5876</eissn><abstract>Increasing evidence suggests that long noncoding RNAs (lncRNAs) play important regulatory roles in biological processes and are dysregulated in numerous tumors. The lncRNA GRASLND functions as an oncogene in many cancers, but its role in skin cutaneous melanoma (SKCM) requires further investigation.
SiRNA transfection, wound - healing and transwell assays were performed to evaluate the effect of GRASLND on cellular function.
The present study demonstrated that GRASLND expression is increased in SKCM tissues and cell lines. The high expression of GRASLND was correlated with poor prognosis and immunotherapy outcomes. Knockdown of GRASLND significantly inhibited cell migration and invasion. In addition, we found that miR-218-5p directly binds to its binding site on GRASLND, and GRASLND and miR-218-5p demonstrate mutual inhibition. Furthermore, the miR-218-5p inhibitor partially eliminated the knockdown of GRASLND and inhibited its expression. We also demonstrated that GRASLND acts as a miR-218-5p sponge that positively regulates STAM2 expression in SKCM cells.
In summary, these data suggest that GRASLND functions by regulating miR-218-5p/STAM2 expression, suggesting an important role for the lncRNA‒miRNA-mRNA functional network and a new potential therapeutic target for SKCM.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>39060946</pmid><doi>10.1186/s12967-024-05397-z</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-5413-8828</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Base Sequence Biological markers Biomarker Care and treatment Cell Line, Tumor Cell Movement - genetics Cell Proliferation - genetics Development and progression Disease Progression Female Gene Expression Regulation, Neoplastic Gene Knockdown Techniques Genetic aspects Humans Immunotherapy lncRNA Male Melanoma Melanoma - genetics Melanoma - metabolism Melanoma - pathology MicroRNAs - genetics MicroRNAs - metabolism Middle Aged Neoplasm Invasiveness Patient outcomes Prognosis RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism SKCM Skin Neoplasms - genetics Skin Neoplasms - metabolism Skin Neoplasms - pathology |
title | GRASLND regulates melanoma cell progression by targeting the miR-218-5p/STAM2 axis |
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