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Exosomal lncRNA LINC01711 facilitates metastasis of esophageal squamous cell carcinoma via the miR-326/FSCN1 axis
Esophageal cancer is a malignant tumor with a five-year survival rate of less than 20%. Early diagnosis and exploration of esophageal cancer pathogenesis are of great significance for the treatment and prognosis of esophageal cancer. Long non-coding RNA (lncRNA) plays a vital role in the occurrence...
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Published in: | Aging (Albany, NY.) NY.), 2021-08, Vol.13 (15), p.19776-19788 |
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description | Esophageal cancer is a malignant tumor with a five-year survival rate of less than 20%. Early diagnosis and exploration of esophageal cancer pathogenesis are of great significance for the treatment and prognosis of esophageal cancer. Long non-coding RNA (lncRNA) plays a vital role in the occurrence and development of different types of tumors. However, the role of exosome LncRNA in esophageal squamous cell carcinoma (ESCC) is rarely reported. In this study, we detected high expression of lncRNA LINC01711 in ESCC tissues and was associated with poor prognosis. Silencing LINC01711 can inhibit the proliferation, migration, invasion, and growth of ESCC cell lines, and induce apoptosis. Linc01711 was identified as a competitive endogenous RNA that suppressed miR-326, and up-regulated the expression of fascin actin-bundling protein 1 (FSCN1). Besides,
experiments showed that the administration of exosome-derived LINC01711 (LINC01711-Exo) promoted the growth of tumors in nude mice. In general, exosomal LINC01711 promoted the proliferation, migration, and invasion of esophageal cancer cells by up-regulating FSCN1 and down-regulating miR-326, thus improved the occurrence and development of ESCC. |
doi_str_mv | 10.18632/aging.203389 |
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experiments showed that the administration of exosome-derived LINC01711 (LINC01711-Exo) promoted the growth of tumors in nude mice. In general, exosomal LINC01711 promoted the proliferation, migration, and invasion of esophageal cancer cells by up-regulating FSCN1 and down-regulating miR-326, thus improved the occurrence and development of ESCC.</description><identifier>ISSN: 1945-4589</identifier><identifier>EISSN: 1945-4589</identifier><identifier>DOI: 10.18632/aging.203389</identifier><identifier>PMID: 34370713</identifier><language>eng</language><publisher>United States: Impact Journals</publisher><subject>Animals ; Apoptosis - physiology ; Carrier Proteins - metabolism ; Cell Line, Tumor ; Cell Movement - physiology ; Cell Proliferation - physiology ; Esophageal Neoplasms - genetics ; Esophageal Neoplasms - metabolism ; Esophageal Neoplasms - pathology ; Esophageal Squamous Cell Carcinoma - genetics ; Esophageal Squamous Cell Carcinoma - metabolism ; Esophageal Squamous Cell Carcinoma - pathology ; Gene Expression Regulation, Neoplastic ; Heterografts ; Humans ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Microfilament Proteins - metabolism ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Neoplasm Invasiveness ; Prognosis ; Research Paper ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; Transfection</subject><ispartof>Aging (Albany, NY.), 2021-08, Vol.13 (15), p.19776-19788</ispartof><rights>Copyright: © 2021 Xu et al.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-2749a4c7c60504e05bc6d2bfef15367400f5b57af14779a42fcb7716d887b0d73</citedby><cites>FETCH-LOGICAL-c387t-2749a4c7c60504e05bc6d2bfef15367400f5b57af14779a42fcb7716d887b0d73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386530/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386530/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34370713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Mei-Ling</creatorcontrib><creatorcontrib>Liu, Tian-Cheng</creatorcontrib><creatorcontrib>Dong, Feng-Xiang</creatorcontrib><creatorcontrib>Meng, Ling-Xin</creatorcontrib><creatorcontrib>Ling, Ai-Xia</creatorcontrib><creatorcontrib>Liu, Shan</creatorcontrib><title>Exosomal lncRNA LINC01711 facilitates metastasis of esophageal squamous cell carcinoma via the miR-326/FSCN1 axis</title><title>Aging (Albany, NY.)</title><addtitle>Aging (Albany NY)</addtitle><description>Esophageal cancer is a malignant tumor with a five-year survival rate of less than 20%. Early diagnosis and exploration of esophageal cancer pathogenesis are of great significance for the treatment and prognosis of esophageal cancer. Long non-coding RNA (lncRNA) plays a vital role in the occurrence and development of different types of tumors. However, the role of exosome LncRNA in esophageal squamous cell carcinoma (ESCC) is rarely reported. In this study, we detected high expression of lncRNA LINC01711 in ESCC tissues and was associated with poor prognosis. Silencing LINC01711 can inhibit the proliferation, migration, invasion, and growth of ESCC cell lines, and induce apoptosis. Linc01711 was identified as a competitive endogenous RNA that suppressed miR-326, and up-regulated the expression of fascin actin-bundling protein 1 (FSCN1). Besides,
experiments showed that the administration of exosome-derived LINC01711 (LINC01711-Exo) promoted the growth of tumors in nude mice. In general, exosomal LINC01711 promoted the proliferation, migration, and invasion of esophageal cancer cells by up-regulating FSCN1 and down-regulating miR-326, thus improved the occurrence and development of ESCC.</description><subject>Animals</subject><subject>Apoptosis - physiology</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - physiology</subject><subject>Cell Proliferation - physiology</subject><subject>Esophageal Neoplasms - genetics</subject><subject>Esophageal Neoplasms - metabolism</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Esophageal Squamous Cell Carcinoma - genetics</subject><subject>Esophageal Squamous Cell Carcinoma - metabolism</subject><subject>Esophageal Squamous Cell Carcinoma - pathology</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Heterografts</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Microfilament Proteins - metabolism</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Neoplasm Invasiveness</subject><subject>Prognosis</subject><subject>Research Paper</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>Transfection</subject><issn>1945-4589</issn><issn>1945-4589</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVkc1LAzEQxYMoflSPXiVHL2uTzdf2IkhpVSgVqp7DbJq0kd1Nu9lK_e-NrYrCQAbyy5s3eQhdUnJDC8nyPix8s7jJCWPF4ACd0gEXGRfF4PBPf4LOYnwjRArB5TE6YZwpoig7RevRNsRQQ4Wrxsymd3jyOB0SqijFDoyvfAedjbi2HcRUPuLgsI1htYSFTa_iegN12ERsbFVhA63xTZLD7x5wt7S49rOM5bI_fh5OKYatj-foyEEV7cX32UOv49HL8CGbPN0_Du8mmWGF6rJc8QFwo4wkgnBLRGnkPC-ddVQwqTghTpRCgaNcqUTmzpRKUTkvClWSuWI9dLvXXW3K2s6NbboWKr1qfQ3thw7g9f-bxi_1IrzrghVSMJIErr8F2rDe2Njp2sevNaGxaWOdC5l-NFmhCc32qGlDjK11v2Mo0buY9C4mvY8p8Vd_vf3SP7mwT8WPjnY</recordid><startdate>20210809</startdate><enddate>20210809</enddate><creator>Xu, Mei-Ling</creator><creator>Liu, Tian-Cheng</creator><creator>Dong, Feng-Xiang</creator><creator>Meng, Ling-Xin</creator><creator>Ling, Ai-Xia</creator><creator>Liu, Shan</creator><general>Impact Journals</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>5PM</scope></search><sort><creationdate>20210809</creationdate><title>Exosomal lncRNA LINC01711 facilitates metastasis of esophageal squamous cell carcinoma via the miR-326/FSCN1 axis</title><author>Xu, Mei-Ling ; Liu, Tian-Cheng ; Dong, Feng-Xiang ; Meng, Ling-Xin ; Ling, Ai-Xia ; Liu, Shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-2749a4c7c60504e05bc6d2bfef15367400f5b57af14779a42fcb7716d887b0d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Apoptosis - physiology</topic><topic>Carrier Proteins - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - physiology</topic><topic>Cell Proliferation - physiology</topic><topic>Esophageal Neoplasms - genetics</topic><topic>Esophageal Neoplasms - metabolism</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Esophageal Squamous Cell Carcinoma - genetics</topic><topic>Esophageal Squamous Cell Carcinoma - metabolism</topic><topic>Esophageal Squamous Cell Carcinoma - pathology</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Heterografts</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Microfilament Proteins - metabolism</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Neoplasm Invasiveness</topic><topic>Prognosis</topic><topic>Research Paper</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>Transfection</topic><toplevel>online_resources</toplevel><creatorcontrib>Xu, Mei-Ling</creatorcontrib><creatorcontrib>Liu, Tian-Cheng</creatorcontrib><creatorcontrib>Dong, Feng-Xiang</creatorcontrib><creatorcontrib>Meng, Ling-Xin</creatorcontrib><creatorcontrib>Ling, Ai-Xia</creatorcontrib><creatorcontrib>Liu, Shan</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>PubMed Central (Full Participant titles)</collection><jtitle>Aging (Albany, NY.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Mei-Ling</au><au>Liu, Tian-Cheng</au><au>Dong, Feng-Xiang</au><au>Meng, Ling-Xin</au><au>Ling, Ai-Xia</au><au>Liu, Shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exosomal lncRNA LINC01711 facilitates metastasis of esophageal squamous cell carcinoma via the miR-326/FSCN1 axis</atitle><jtitle>Aging (Albany, NY.)</jtitle><addtitle>Aging (Albany NY)</addtitle><date>2021-08-09</date><risdate>2021</risdate><volume>13</volume><issue>15</issue><spage>19776</spage><epage>19788</epage><pages>19776-19788</pages><issn>1945-4589</issn><eissn>1945-4589</eissn><abstract>Esophageal cancer is a malignant tumor with a five-year survival rate of less than 20%. Early diagnosis and exploration of esophageal cancer pathogenesis are of great significance for the treatment and prognosis of esophageal cancer. Long non-coding RNA (lncRNA) plays a vital role in the occurrence and development of different types of tumors. However, the role of exosome LncRNA in esophageal squamous cell carcinoma (ESCC) is rarely reported. In this study, we detected high expression of lncRNA LINC01711 in ESCC tissues and was associated with poor prognosis. Silencing LINC01711 can inhibit the proliferation, migration, invasion, and growth of ESCC cell lines, and induce apoptosis. Linc01711 was identified as a competitive endogenous RNA that suppressed miR-326, and up-regulated the expression of fascin actin-bundling protein 1 (FSCN1). Besides,
experiments showed that the administration of exosome-derived LINC01711 (LINC01711-Exo) promoted the growth of tumors in nude mice. In general, exosomal LINC01711 promoted the proliferation, migration, and invasion of esophageal cancer cells by up-regulating FSCN1 and down-regulating miR-326, thus improved the occurrence and development of ESCC.</abstract><cop>United States</cop><pub>Impact Journals</pub><pmid>34370713</pmid><doi>10.18632/aging.203389</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis - physiology Carrier Proteins - metabolism Cell Line, Tumor Cell Movement - physiology Cell Proliferation - physiology Esophageal Neoplasms - genetics Esophageal Neoplasms - metabolism Esophageal Neoplasms - pathology Esophageal Squamous Cell Carcinoma - genetics Esophageal Squamous Cell Carcinoma - metabolism Esophageal Squamous Cell Carcinoma - pathology Gene Expression Regulation, Neoplastic Heterografts Humans Mice Mice, Inbred BALB C Mice, Nude Microfilament Proteins - metabolism MicroRNAs - genetics MicroRNAs - metabolism Neoplasm Invasiveness Prognosis Research Paper RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism Transfection |
title | Exosomal lncRNA LINC01711 facilitates metastasis of esophageal squamous cell carcinoma via the miR-326/FSCN1 axis |
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