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Exosomal miR-155-5p promotes proliferation and migration of gastric cancer cells by inhibiting TP53INP1 expression
Exosomal microRNA (miRNA) secreted by tumor cells plays an important biological role in tumorigenesis and development. We aimed to explore the effects of exosomal miR-155-5p in gastric cancer (GC) and understand its mechanism of action in GC progression. We isolated exosomes from the human gastric m...
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Published in: | Pathology, research and practice research and practice, 2020-06, Vol.216 (6), p.152986-152986, Article 152986 |
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description | Exosomal microRNA (miRNA) secreted by tumor cells plays an important biological role in tumorigenesis and development. We aimed to explore the effects of exosomal miR-155-5p in gastric cancer (GC) and understand its mechanism of action in GC progression. We isolated exosomes from the human gastric mucosal epithelial cell line GES-1 and gastric cancer cell line AGS, and then identified them according to their surface markers by flow cytometry. Later, we detected the miR-155-5p expression levels in tissues and isolated exosomes using RT-qPCR. Bioinformatics analysis showed that miR-155-5p directly binds to the 3' untranslated region (3'-UTR) of tumor protein p53-induced nuclear protein 1 (TP53INP1) mRNA. We also investigated whether the miR-155-5p-rich exosomes caused changes in cell cycle, proliferation, and migration in AGS cells. In this study, we found that the levels of miR-155-5p were significantly increased in GC tissues and AGS cells, and that the TP53INP1 protein level was downregulated in GC tissues using IHC and IFC. TP53INP1 was found to be directly regulated by miR-155-5p following a dual luciferase-based reporter assay. After co-culturing with the isolated miR-155-5p-rich exosomes, the proliferation and migration capabilities of AGS cells were enhanced. Thus, our results reveal that exosomal miR-155-5p acts as an oncogene by targeting TP53INP1 mRNA in human gastric cancer. |
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We aimed to explore the effects of exosomal miR-155-5p in gastric cancer (GC) and understand its mechanism of action in GC progression. We isolated exosomes from the human gastric mucosal epithelial cell line GES-1 and gastric cancer cell line AGS, and then identified them according to their surface markers by flow cytometry. Later, we detected the miR-155-5p expression levels in tissues and isolated exosomes using RT-qPCR. Bioinformatics analysis showed that miR-155-5p directly binds to the 3' untranslated region (3'-UTR) of tumor protein p53-induced nuclear protein 1 (TP53INP1) mRNA. We also investigated whether the miR-155-5p-rich exosomes caused changes in cell cycle, proliferation, and migration in AGS cells. In this study, we found that the levels of miR-155-5p were significantly increased in GC tissues and AGS cells, and that the TP53INP1 protein level was downregulated in GC tissues using IHC and IFC. TP53INP1 was found to be directly regulated by miR-155-5p following a dual luciferase-based reporter assay. After co-culturing with the isolated miR-155-5p-rich exosomes, the proliferation and migration capabilities of AGS cells were enhanced. Thus, our results reveal that exosomal miR-155-5p acts as an oncogene by targeting TP53INP1 mRNA in human gastric cancer.</description><identifier>ISSN: 0344-0338</identifier><identifier>EISSN: 1618-0631</identifier><identifier>DOI: 10.1016/j.prp.2020.152986</identifier><identifier>PMID: 32527448</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>55-5p ; Carrier Proteins - biosynthesis ; Cell Line, Tumor ; Cell Movement - genetics ; Cell Proliferation - genetics ; Down-Regulation ; exosome ; Exosomes - genetics ; gastric cancer ; Gene Expression Regulation, Neoplastic - genetics ; Heat-Shock Proteins - biosynthesis ; Humans ; MicroRNAs - genetics ; miR-1 ; Oncogenes - genetics ; Stomach Neoplasms - genetics ; Stomach Neoplasms - metabolism ; Stomach Neoplasms - pathology ; tumor protein p53-induced nuclear protein 1</subject><ispartof>Pathology, research and practice, 2020-06, Vol.216 (6), p.152986-152986, Article 152986</ispartof><rights>2020 Elsevier GmbH</rights><rights>Copyright © 2020 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-80f79c22c9122a1d333747aa9e6f5ea4a80352ac68e265cd76c3a16f3c7538313</citedby><cites>FETCH-LOGICAL-c353t-80f79c22c9122a1d333747aa9e6f5ea4a80352ac68e265cd76c3a16f3c7538313</cites></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/32527448$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Shuai-Shuai</creatorcontrib><creatorcontrib>Zhang, Hui-Peng</creatorcontrib><creatorcontrib>Yang, Chang-Qing</creatorcontrib><creatorcontrib>Li, Li-Na</creatorcontrib><creatorcontrib>Shen, Yu</creatorcontrib><creatorcontrib>Zhang, Yi-Qiang</creatorcontrib><title>Exosomal miR-155-5p promotes proliferation and migration of gastric cancer cells by inhibiting TP53INP1 expression</title><title>Pathology, research and practice</title><addtitle>Pathol Res Pract</addtitle><description>Exosomal microRNA (miRNA) secreted by tumor cells plays an important biological role in tumorigenesis and development. We aimed to explore the effects of exosomal miR-155-5p in gastric cancer (GC) and understand its mechanism of action in GC progression. We isolated exosomes from the human gastric mucosal epithelial cell line GES-1 and gastric cancer cell line AGS, and then identified them according to their surface markers by flow cytometry. Later, we detected the miR-155-5p expression levels in tissues and isolated exosomes using RT-qPCR. Bioinformatics analysis showed that miR-155-5p directly binds to the 3' untranslated region (3'-UTR) of tumor protein p53-induced nuclear protein 1 (TP53INP1) mRNA. We also investigated whether the miR-155-5p-rich exosomes caused changes in cell cycle, proliferation, and migration in AGS cells. In this study, we found that the levels of miR-155-5p were significantly increased in GC tissues and AGS cells, and that the TP53INP1 protein level was downregulated in GC tissues using IHC and IFC. TP53INP1 was found to be directly regulated by miR-155-5p following a dual luciferase-based reporter assay. After co-culturing with the isolated miR-155-5p-rich exosomes, the proliferation and migration capabilities of AGS cells were enhanced. Thus, our results reveal that exosomal miR-155-5p acts as an oncogene by targeting TP53INP1 mRNA in human gastric cancer.</description><subject>55-5p</subject><subject>Carrier Proteins - biosynthesis</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - genetics</subject><subject>Cell Proliferation - genetics</subject><subject>Down-Regulation</subject><subject>exosome</subject><subject>Exosomes - genetics</subject><subject>gastric cancer</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Heat-Shock Proteins - biosynthesis</subject><subject>Humans</subject><subject>MicroRNAs - genetics</subject><subject>miR-1</subject><subject>Oncogenes - genetics</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - metabolism</subject><subject>Stomach Neoplasms - pathology</subject><subject>tumor protein p53-induced nuclear protein 1</subject><issn>0344-0338</issn><issn>1618-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kMFO3DAQhq2qqGyhD9BL5WMvWTye2EnEqUJAkRCgCs6W15lsvUriYGcRvH292qVHTvZY3__L8zH2HcQSBOizzXKK01IKmWclm1p_YgvQUBdCI3xmC4FlWQjE-ph9TWkjhKhECV_YMUolq7KsFyxevoYUBtvzwf8pQKlCTXyKYQgzpd2l9x1FO_swcju2mVofptDxtU1z9I47OzqK3FHfJ756437861d-9uOaPz4ovLl7AE6vU6SUcvKUHXW2T_TtcJ6wp6vLx4vfxe399c3Fr9vCocK5qEVXNU5K14CUFlpErMrK2oZ0p8iWthaopHW6JqmVayvt0ILu0FUKawQ8YT_3vXmL5y2l2Qw-7f5oRwrbZGQJsmkUgMgo7FEXQ0qROjNFP9j4ZkCYnWqzyS-T2ak2e9U58-NQv10N1P5PvLvNwPkeoLzki6dokvOUTbU-kptNG_wH9f8A9xOOQw</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>Shi, Shuai-Shuai</creator><creator>Zhang, Hui-Peng</creator><creator>Yang, Chang-Qing</creator><creator>Li, Li-Na</creator><creator>Shen, Yu</creator><creator>Zhang, Yi-Qiang</creator><general>Elsevier GmbH</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></search><sort><creationdate>202006</creationdate><title>Exosomal miR-155-5p promotes proliferation and migration of gastric cancer cells by inhibiting TP53INP1 expression</title><author>Shi, Shuai-Shuai ; Zhang, Hui-Peng ; Yang, Chang-Qing ; Li, Li-Na ; Shen, Yu ; Zhang, Yi-Qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-80f79c22c9122a1d333747aa9e6f5ea4a80352ac68e265cd76c3a16f3c7538313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>55-5p</topic><topic>Carrier Proteins - biosynthesis</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - genetics</topic><topic>Cell Proliferation - genetics</topic><topic>Down-Regulation</topic><topic>exosome</topic><topic>Exosomes - genetics</topic><topic>gastric cancer</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Heat-Shock Proteins - biosynthesis</topic><topic>Humans</topic><topic>MicroRNAs - genetics</topic><topic>miR-1</topic><topic>Oncogenes - genetics</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - metabolism</topic><topic>Stomach Neoplasms - pathology</topic><topic>tumor protein p53-induced nuclear protein 1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Shuai-Shuai</creatorcontrib><creatorcontrib>Zhang, Hui-Peng</creatorcontrib><creatorcontrib>Yang, Chang-Qing</creatorcontrib><creatorcontrib>Li, Li-Na</creatorcontrib><creatorcontrib>Shen, Yu</creatorcontrib><creatorcontrib>Zhang, Yi-Qiang</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><jtitle>Pathology, research and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Shuai-Shuai</au><au>Zhang, Hui-Peng</au><au>Yang, Chang-Qing</au><au>Li, Li-Na</au><au>Shen, Yu</au><au>Zhang, Yi-Qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exosomal miR-155-5p promotes proliferation and migration of gastric cancer cells by inhibiting TP53INP1 expression</atitle><jtitle>Pathology, research and practice</jtitle><addtitle>Pathol Res Pract</addtitle><date>2020-06</date><risdate>2020</risdate><volume>216</volume><issue>6</issue><spage>152986</spage><epage>152986</epage><pages>152986-152986</pages><artnum>152986</artnum><issn>0344-0338</issn><eissn>1618-0631</eissn><abstract>Exosomal microRNA (miRNA) secreted by tumor cells plays an important biological role in tumorigenesis and development. We aimed to explore the effects of exosomal miR-155-5p in gastric cancer (GC) and understand its mechanism of action in GC progression. We isolated exosomes from the human gastric mucosal epithelial cell line GES-1 and gastric cancer cell line AGS, and then identified them according to their surface markers by flow cytometry. Later, we detected the miR-155-5p expression levels in tissues and isolated exosomes using RT-qPCR. Bioinformatics analysis showed that miR-155-5p directly binds to the 3' untranslated region (3'-UTR) of tumor protein p53-induced nuclear protein 1 (TP53INP1) mRNA. We also investigated whether the miR-155-5p-rich exosomes caused changes in cell cycle, proliferation, and migration in AGS cells. In this study, we found that the levels of miR-155-5p were significantly increased in GC tissues and AGS cells, and that the TP53INP1 protein level was downregulated in GC tissues using IHC and IFC. TP53INP1 was found to be directly regulated by miR-155-5p following a dual luciferase-based reporter assay. After co-culturing with the isolated miR-155-5p-rich exosomes, the proliferation and migration capabilities of AGS cells were enhanced. Thus, our results reveal that exosomal miR-155-5p acts as an oncogene by targeting TP53INP1 mRNA in human gastric cancer.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>32527448</pmid><doi>10.1016/j.prp.2020.152986</doi><tpages>1</tpages></addata></record> |
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subjects | 55-5p Carrier Proteins - biosynthesis Cell Line, Tumor Cell Movement - genetics Cell Proliferation - genetics Down-Regulation exosome Exosomes - genetics gastric cancer Gene Expression Regulation, Neoplastic - genetics Heat-Shock Proteins - biosynthesis Humans MicroRNAs - genetics miR-1 Oncogenes - genetics Stomach Neoplasms - genetics Stomach Neoplasms - metabolism Stomach Neoplasms - pathology tumor protein p53-induced nuclear protein 1 |
title | Exosomal miR-155-5p promotes proliferation and migration of gastric cancer cells by inhibiting TP53INP1 expression |
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