miR-223-3p promotes cell proliferation and invasion by targeting Arid1a in gastric cancer
Abstract Accumulating evidence has indicated that microRNAs can regulate downstream signaling pathways and play an important role in various tumors. In this study, we found that miR-223-3p was differentially expressed in 40 paired gastric cancer tissues and adjacent tissues and that miR-223-3p was p...
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Veröffentlicht in: | Acta biochimica et biophysica Sinica 2020-02, Vol.52 (2), p.150-159 |
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creator | Zhu, Yiping Li, Kai Yan, Liang He, Yang Wang, Lu Sheng, Lili |
description | Abstract
Accumulating evidence has indicated that microRNAs can regulate downstream signaling pathways and play an important role in various tumors. In this study, we found that miR-223-3p was differentially expressed in 40 paired gastric cancer tissues and adjacent tissues and that miR-223-3p was positively correlated with tumor invasion depth and lymph node metastasis. Luciferase reporter assay confirmed that Arid1a was the target gene of miR-223-3p. Functional assays showed that miR-223-3p promoted the proliferation and invasion of gastric cancer cells by regulating the expression of Arid1a. We also confirmed that miR-223-3p regulated the growth of gastric cancer cells in vivo, while an antagomir against miR-223-3p significantly inhibited tumor growth. In conclusion, our results demonstrated that miR-223-3p inhibits gastric cancer cell progression by decreasing the expression of Arid1a. Therefore, miR-223-3p may act as a potential therapeutic target for patients with gastric cancer. |
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Accumulating evidence has indicated that microRNAs can regulate downstream signaling pathways and play an important role in various tumors. In this study, we found that miR-223-3p was differentially expressed in 40 paired gastric cancer tissues and adjacent tissues and that miR-223-3p was positively correlated with tumor invasion depth and lymph node metastasis. Luciferase reporter assay confirmed that Arid1a was the target gene of miR-223-3p. Functional assays showed that miR-223-3p promoted the proliferation and invasion of gastric cancer cells by regulating the expression of Arid1a. We also confirmed that miR-223-3p regulated the growth of gastric cancer cells in vivo, while an antagomir against miR-223-3p significantly inhibited tumor growth. In conclusion, our results demonstrated that miR-223-3p inhibits gastric cancer cell progression by decreasing the expression of Arid1a. Therefore, miR-223-3p may act as a potential therapeutic target for patients with gastric cancer.</description><identifier>ISSN: 1672-9145</identifier><identifier>EISSN: 1745-7270</identifier><identifier>DOI: 10.1093/abbs/gmz151</identifier><identifier>PMID: 31912865</identifier><language>eng</language><publisher>China: Oxford University Press</publisher><ispartof>Acta biochimica et biophysica Sinica, 2020-02, Vol.52 (2), p.150-159</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-3fbbcc0b427e1efa36657bd2cd2fdf3b904935cf2f4595107bf9d4087bd0dfe63</citedby><cites>FETCH-LOGICAL-c386t-3fbbcc0b427e1efa36657bd2cd2fdf3b904935cf2f4595107bf9d4087bd0dfe63</cites><orcidid>0000-0002-2560-4252</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31912865$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yiping</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Yan, Liang</creatorcontrib><creatorcontrib>He, Yang</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Sheng, Lili</creatorcontrib><title>miR-223-3p promotes cell proliferation and invasion by targeting Arid1a in gastric cancer</title><title>Acta biochimica et biophysica Sinica</title><addtitle>Acta Biochim Biophys Sin (Shanghai)</addtitle><description>Abstract
Accumulating evidence has indicated that microRNAs can regulate downstream signaling pathways and play an important role in various tumors. In this study, we found that miR-223-3p was differentially expressed in 40 paired gastric cancer tissues and adjacent tissues and that miR-223-3p was positively correlated with tumor invasion depth and lymph node metastasis. Luciferase reporter assay confirmed that Arid1a was the target gene of miR-223-3p. Functional assays showed that miR-223-3p promoted the proliferation and invasion of gastric cancer cells by regulating the expression of Arid1a. We also confirmed that miR-223-3p regulated the growth of gastric cancer cells in vivo, while an antagomir against miR-223-3p significantly inhibited tumor growth. In conclusion, our results demonstrated that miR-223-3p inhibits gastric cancer cell progression by decreasing the expression of Arid1a. Therefore, miR-223-3p may act as a potential therapeutic target for patients with gastric cancer.</description><issn>1672-9145</issn><issn>1745-7270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLxDAUhYMozji6ci9ZiSB18miaZjkMvmBAEF24KnmWSF8mrTD-eluqLl3de7gfh3MPAOcY3WAk6FoqFddl_YUZPgBLzFOWcMLR4bhnnCQCp2wBTmJ8R4hmGUbHYEGxwCTP2BK81f45IYQmtINdaOu2txFqW1WTqryzQfa-baBsDPTNp4yTUHvYy1Da3jcl3ARvsByPsJSxD15DLRttwyk4crKK9uxnrsDr3e3L9iHZPd0_bje7RNM86xPqlNIaqZRwi62TY0TGlSHaEGccVQKlgjLtiEuZYBhx5YRJUT4yyDib0RW4mn3HwB-DjX1R-zh9IBvbDrEglKaZyBmf0OsZ1aGNMVhXdMHXMuwLjIqpy2Lqspi7HOmLH-NB1db8sb_ljcDlDLRD96_TN_2_fhI</recordid><startdate>20200203</startdate><enddate>20200203</enddate><creator>Zhu, Yiping</creator><creator>Li, Kai</creator><creator>Yan, Liang</creator><creator>He, Yang</creator><creator>Wang, Lu</creator><creator>Sheng, Lili</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2560-4252</orcidid></search><sort><creationdate>20200203</creationdate><title>miR-223-3p promotes cell proliferation and invasion by targeting Arid1a in gastric cancer</title><author>Zhu, Yiping ; Li, Kai ; Yan, Liang ; He, Yang ; Wang, Lu ; Sheng, Lili</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-3fbbcc0b427e1efa36657bd2cd2fdf3b904935cf2f4595107bf9d4087bd0dfe63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yiping</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Yan, Liang</creatorcontrib><creatorcontrib>He, Yang</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Sheng, Lili</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Acta biochimica et biophysica Sinica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Yiping</au><au>Li, Kai</au><au>Yan, Liang</au><au>He, Yang</au><au>Wang, Lu</au><au>Sheng, Lili</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miR-223-3p promotes cell proliferation and invasion by targeting Arid1a in gastric cancer</atitle><jtitle>Acta biochimica et biophysica Sinica</jtitle><addtitle>Acta Biochim Biophys Sin (Shanghai)</addtitle><date>2020-02-03</date><risdate>2020</risdate><volume>52</volume><issue>2</issue><spage>150</spage><epage>159</epage><pages>150-159</pages><issn>1672-9145</issn><eissn>1745-7270</eissn><abstract>Abstract
Accumulating evidence has indicated that microRNAs can regulate downstream signaling pathways and play an important role in various tumors. In this study, we found that miR-223-3p was differentially expressed in 40 paired gastric cancer tissues and adjacent tissues and that miR-223-3p was positively correlated with tumor invasion depth and lymph node metastasis. Luciferase reporter assay confirmed that Arid1a was the target gene of miR-223-3p. Functional assays showed that miR-223-3p promoted the proliferation and invasion of gastric cancer cells by regulating the expression of Arid1a. We also confirmed that miR-223-3p regulated the growth of gastric cancer cells in vivo, while an antagomir against miR-223-3p significantly inhibited tumor growth. In conclusion, our results demonstrated that miR-223-3p inhibits gastric cancer cell progression by decreasing the expression of Arid1a. Therefore, miR-223-3p may act as a potential therapeutic target for patients with gastric cancer.</abstract><cop>China</cop><pub>Oxford University Press</pub><pmid>31912865</pmid><doi>10.1093/abbs/gmz151</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2560-4252</orcidid></addata></record> |
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title | miR-223-3p promotes cell proliferation and invasion by targeting Arid1a in gastric cancer |
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