Long Non-Coding RNA NEAT1 Serves as Sponge for miR-365a-3p to Promote Gastric Cancer Progression via Regulating ABCC4

Long non-coding RNA (lncRNA) was reported to be a crucial regulator in cancer. In this work, our purpose is to explore the biological roles of nuclear paraspeckle assembly transcript 1 (NEAT1) in gastric cancer (GC). Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to detect...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:OncoTargets and therapy 2020-01, Vol.13, p.3977-3985
Hauptverfasser: Gao, Ming, Liu, Liying, Zhang, Dianbao, Yang, Yudan, Chang, Zhiwei
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3985
container_issue
container_start_page 3977
container_title OncoTargets and therapy
container_volume 13
creator Gao, Ming
Liu, Liying
Zhang, Dianbao
Yang, Yudan
Chang, Zhiwei
description Long non-coding RNA (lncRNA) was reported to be a crucial regulator in cancer. In this work, our purpose is to explore the biological roles of nuclear paraspeckle assembly transcript 1 (NEAT1) in gastric cancer (GC). Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to detect NEAT1 expression in GC cells and normal cells. GC cell behaviors after NEAT1 overexpression or downregulation were analyzed by Cell Counting Kit-8 assay, colony formation assay, wound-healing assay, and flow cytometry assay. Bioinformatic tools were used to analyze the significance of NEAT1 in GC. The involvement of microRNA-365a-3p (miR-365a-3p) and ATP-binding cassette subfamily C member 4 (ABCC4) in the biological roles of NEAT1 in GC progression was validated by luciferase activity reporter assay and rescue experiments. We found NEAT1 increased expression in both GC tissues and cells and correlated with poorer overall survival of cancer patients. We found NEAT1 overexpression promotes, while its knockdown inhibits GC cell proliferation, colony formation, invasion, and cell cycle progression in vitro. Mechanism analyses showed that NEAT1 serves as a ceRNA to upregulate ABCC4 expression via sponging miR-365a-3p. In this study, we revealed a NEAT1/miR-365a-3p/ABCC4 triplet in GC progression, which may provide novel targeted therapy markers for GC.
doi_str_mv 10.2147/OTT.S245557
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7227816</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2409638765</sourcerecordid><originalsourceid>FETCH-LOGICAL-c381t-679980d59f7e3482bdede4f54ede9150e85b12fc4d75739a04bd76e8f466b2313</originalsourceid><addsrcrecordid>eNpVkUtr3DAUhUVpaB7tqvugZaE40VvyJjA1ecEwKTPTtZDt66mCbU0keyD_Ph4yCcnqHO79OPfCQegnJReMCn35sF5frJiQUuov6IRSbTKVc_L1gz9Gpyk9EqKUYeIbOuZM5IJKfoLGeeg3eBH6rAi1n-xyMcOL69ma4hXEHSTsEl5tJwhwEyLu_DLjSrqMb_EQ8N8YujAAvnVpiL7ChesriPvxJkJKPvR45x1ewmZs3bDPn_0pCvEdHTWuTfDjoGfo3831urjL5g-398VsnlXc0CFTOs8NqWXeaODCsLKGGkQjxSQ5lQSMLClrKlFrqXnuiChrrcA0QqmSccrP0NVr7nYsO6gr6IfoWruNvnPx2Qbn7edN7__bTdhZzZg2VE0Bvw4BMTyNkAbb-VRB27oewpgsEyRX3GglJ_T3K1rFkFKE5v0MJXZflJ2KsoeiJvr842fv7Fsz_AW_Ro0w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2409638765</pqid></control><display><type>article</type><title>Long Non-Coding RNA NEAT1 Serves as Sponge for miR-365a-3p to Promote Gastric Cancer Progression via Regulating ABCC4</title><source>Dove Press Free</source><source>PubMed Central Open Access</source><source>Access via Taylor &amp; Francis (Open Access Collection)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Gao, Ming ; Liu, Liying ; Zhang, Dianbao ; Yang, Yudan ; Chang, Zhiwei</creator><creatorcontrib>Gao, Ming ; Liu, Liying ; Zhang, Dianbao ; Yang, Yudan ; Chang, Zhiwei</creatorcontrib><description>Long non-coding RNA (lncRNA) was reported to be a crucial regulator in cancer. In this work, our purpose is to explore the biological roles of nuclear paraspeckle assembly transcript 1 (NEAT1) in gastric cancer (GC). Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to detect NEAT1 expression in GC cells and normal cells. GC cell behaviors after NEAT1 overexpression or downregulation were analyzed by Cell Counting Kit-8 assay, colony formation assay, wound-healing assay, and flow cytometry assay. Bioinformatic tools were used to analyze the significance of NEAT1 in GC. The involvement of microRNA-365a-3p (miR-365a-3p) and ATP-binding cassette subfamily C member 4 (ABCC4) in the biological roles of NEAT1 in GC progression was validated by luciferase activity reporter assay and rescue experiments. We found NEAT1 increased expression in both GC tissues and cells and correlated with poorer overall survival of cancer patients. We found NEAT1 overexpression promotes, while its knockdown inhibits GC cell proliferation, colony formation, invasion, and cell cycle progression in vitro. Mechanism analyses showed that NEAT1 serves as a ceRNA to upregulate ABCC4 expression via sponging miR-365a-3p. In this study, we revealed a NEAT1/miR-365a-3p/ABCC4 triplet in GC progression, which may provide novel targeted therapy markers for GC.</description><identifier>ISSN: 1178-6930</identifier><identifier>EISSN: 1178-6930</identifier><identifier>DOI: 10.2147/OTT.S245557</identifier><identifier>PMID: 32494153</identifier><language>eng</language><publisher>New Zealand: Dove</publisher><subject>Original Research</subject><ispartof>OncoTargets and therapy, 2020-01, Vol.13, p.3977-3985</ispartof><rights>2020 Gao et al.</rights><rights>2020 Gao et al. 2020 Gao et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-679980d59f7e3482bdede4f54ede9150e85b12fc4d75739a04bd76e8f466b2313</citedby><cites>FETCH-LOGICAL-c381t-679980d59f7e3482bdede4f54ede9150e85b12fc4d75739a04bd76e8f466b2313</cites><orcidid>0000-0001-5050-2939</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227816/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227816/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3862,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32494153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Ming</creatorcontrib><creatorcontrib>Liu, Liying</creatorcontrib><creatorcontrib>Zhang, Dianbao</creatorcontrib><creatorcontrib>Yang, Yudan</creatorcontrib><creatorcontrib>Chang, Zhiwei</creatorcontrib><title>Long Non-Coding RNA NEAT1 Serves as Sponge for miR-365a-3p to Promote Gastric Cancer Progression via Regulating ABCC4</title><title>OncoTargets and therapy</title><addtitle>Onco Targets Ther</addtitle><description>Long non-coding RNA (lncRNA) was reported to be a crucial regulator in cancer. In this work, our purpose is to explore the biological roles of nuclear paraspeckle assembly transcript 1 (NEAT1) in gastric cancer (GC). Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to detect NEAT1 expression in GC cells and normal cells. GC cell behaviors after NEAT1 overexpression or downregulation were analyzed by Cell Counting Kit-8 assay, colony formation assay, wound-healing assay, and flow cytometry assay. Bioinformatic tools were used to analyze the significance of NEAT1 in GC. The involvement of microRNA-365a-3p (miR-365a-3p) and ATP-binding cassette subfamily C member 4 (ABCC4) in the biological roles of NEAT1 in GC progression was validated by luciferase activity reporter assay and rescue experiments. We found NEAT1 increased expression in both GC tissues and cells and correlated with poorer overall survival of cancer patients. We found NEAT1 overexpression promotes, while its knockdown inhibits GC cell proliferation, colony formation, invasion, and cell cycle progression in vitro. Mechanism analyses showed that NEAT1 serves as a ceRNA to upregulate ABCC4 expression via sponging miR-365a-3p. In this study, we revealed a NEAT1/miR-365a-3p/ABCC4 triplet in GC progression, which may provide novel targeted therapy markers for GC.</description><subject>Original Research</subject><issn>1178-6930</issn><issn>1178-6930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVkUtr3DAUhUVpaB7tqvugZaE40VvyJjA1ecEwKTPTtZDt66mCbU0keyD_Ph4yCcnqHO79OPfCQegnJReMCn35sF5frJiQUuov6IRSbTKVc_L1gz9Gpyk9EqKUYeIbOuZM5IJKfoLGeeg3eBH6rAi1n-xyMcOL69ma4hXEHSTsEl5tJwhwEyLu_DLjSrqMb_EQ8N8YujAAvnVpiL7ChesriPvxJkJKPvR45x1ewmZs3bDPn_0pCvEdHTWuTfDjoGfo3831urjL5g-398VsnlXc0CFTOs8NqWXeaODCsLKGGkQjxSQ5lQSMLClrKlFrqXnuiChrrcA0QqmSccrP0NVr7nYsO6gr6IfoWruNvnPx2Qbn7edN7__bTdhZzZg2VE0Bvw4BMTyNkAbb-VRB27oewpgsEyRX3GglJ_T3K1rFkFKE5v0MJXZflJ2KsoeiJvr842fv7Fsz_AW_Ro0w</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Gao, Ming</creator><creator>Liu, Liying</creator><creator>Zhang, Dianbao</creator><creator>Yang, Yudan</creator><creator>Chang, Zhiwei</creator><general>Dove</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5050-2939</orcidid></search><sort><creationdate>20200101</creationdate><title>Long Non-Coding RNA NEAT1 Serves as Sponge for miR-365a-3p to Promote Gastric Cancer Progression via Regulating ABCC4</title><author>Gao, Ming ; Liu, Liying ; Zhang, Dianbao ; Yang, Yudan ; Chang, Zhiwei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-679980d59f7e3482bdede4f54ede9150e85b12fc4d75739a04bd76e8f466b2313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Original Research</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Ming</creatorcontrib><creatorcontrib>Liu, Liying</creatorcontrib><creatorcontrib>Zhang, Dianbao</creatorcontrib><creatorcontrib>Yang, Yudan</creatorcontrib><creatorcontrib>Chang, Zhiwei</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>OncoTargets and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Ming</au><au>Liu, Liying</au><au>Zhang, Dianbao</au><au>Yang, Yudan</au><au>Chang, Zhiwei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long Non-Coding RNA NEAT1 Serves as Sponge for miR-365a-3p to Promote Gastric Cancer Progression via Regulating ABCC4</atitle><jtitle>OncoTargets and therapy</jtitle><addtitle>Onco Targets Ther</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>13</volume><spage>3977</spage><epage>3985</epage><pages>3977-3985</pages><issn>1178-6930</issn><eissn>1178-6930</eissn><abstract>Long non-coding RNA (lncRNA) was reported to be a crucial regulator in cancer. In this work, our purpose is to explore the biological roles of nuclear paraspeckle assembly transcript 1 (NEAT1) in gastric cancer (GC). Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to detect NEAT1 expression in GC cells and normal cells. GC cell behaviors after NEAT1 overexpression or downregulation were analyzed by Cell Counting Kit-8 assay, colony formation assay, wound-healing assay, and flow cytometry assay. Bioinformatic tools were used to analyze the significance of NEAT1 in GC. The involvement of microRNA-365a-3p (miR-365a-3p) and ATP-binding cassette subfamily C member 4 (ABCC4) in the biological roles of NEAT1 in GC progression was validated by luciferase activity reporter assay and rescue experiments. We found NEAT1 increased expression in both GC tissues and cells and correlated with poorer overall survival of cancer patients. We found NEAT1 overexpression promotes, while its knockdown inhibits GC cell proliferation, colony formation, invasion, and cell cycle progression in vitro. Mechanism analyses showed that NEAT1 serves as a ceRNA to upregulate ABCC4 expression via sponging miR-365a-3p. In this study, we revealed a NEAT1/miR-365a-3p/ABCC4 triplet in GC progression, which may provide novel targeted therapy markers for GC.</abstract><cop>New Zealand</cop><pub>Dove</pub><pmid>32494153</pmid><doi>10.2147/OTT.S245557</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5050-2939</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1178-6930
ispartof OncoTargets and therapy, 2020-01, Vol.13, p.3977-3985
issn 1178-6930
1178-6930
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7227816
source Dove Press Free; PubMed Central Open Access; Access via Taylor & Francis (Open Access Collection); EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Original Research
title Long Non-Coding RNA NEAT1 Serves as Sponge for miR-365a-3p to Promote Gastric Cancer Progression via Regulating ABCC4
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T22%3A17%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long%20Non-Coding%20RNA%20NEAT1%20Serves%20as%20Sponge%20for%20miR-365a-3p%20to%20Promote%20Gastric%20Cancer%20Progression%20via%20Regulating%20ABCC4&rft.jtitle=OncoTargets%20and%20therapy&rft.au=Gao,%20Ming&rft.date=2020-01-01&rft.volume=13&rft.spage=3977&rft.epage=3985&rft.pages=3977-3985&rft.issn=1178-6930&rft.eissn=1178-6930&rft_id=info:doi/10.2147/OTT.S245557&rft_dat=%3Cproquest_pubme%3E2409638765%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2409638765&rft_id=info:pmid/32494153&rfr_iscdi=true