Matches in SemOpenAlex for { <https://semopenalex.org/work/W2891333318> ?p ?o ?g. }
- W2891333318 endingPage "5752" @default.
- W2891333318 startingPage "5743" @default.
- W2891333318 abstract "Long noncoding RNA SNHG6 promotes the progression of colorectal cancer through sponging miR-760 and activation of FOXC1 Yuekun Zhu,1,* Yanwei Xing,1,* Fengxu Chi,1 Weidong Sun,1 Zhiyong Zhang,2 Daxun Piao1 1Department of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, China; 2Department of Surgery, Robert-Wood-Johnson Medical School University Hospital, Rutgers University, The State University of New Jersey, New Brunswick, NJ, USA *These authors contributed equally to this work Background: Colorectal cancer (CRC) is one of most common cancers worldwide. Long non-coding RNA SNHG6 has been reported to act as essential regulators in several cancers. However, the functional role and molecular mechanism of SNHG6 in colorectal cancer remain unclear. Methods: Quantitative real-time polymerase chain reaction (PCR) was performed to evaluate the SNHG6 expression in CRC tissues. Colony formation, transwell assays and in vivo mice models were carried out to assess the effect of SNHG6 on CRC biological functions. Results: In the present study, we showed that the expression of SNHG6 was significantly upregulated in CRC tissues and cell lines. High expression of SNHG6 was associated with shorter overall survival in CRC patients. Functionally, SNHG6 knockdown significantly inhibited cell proliferation, invasion and migration both in vitro and in vivo. Mechanically, miR-760 was a direct target of SNHG6, and repression of miR-760 could rescue the inhibitory effect of SNHG6 knockdown on CRC progression. In addition, SNHG6 positively regulated FOXC1 expression through sponging miR-760 in CRC cells, thus indicating that SNHG6 exerted an oncogenic role in CRC by acting as a ceRNA of miR-760. Conclusion: Our results indicate that long non-coding RNA SNHG6 promotes colorectal cancer progression by sequestering miR-760 and activating FOXC1, our findings suggest that SNHG6 may serve as a potential therapeutic target for CRC. Keywords: lncRNA SNHG6, miR-760, FOXC1, colorectal cancer" @default.
- W2891333318 created "2018-09-27" @default.
- W2891333318 creator A5002577443 @default.
- W2891333318 creator A5035687873 @default.
- W2891333318 creator A5050602839 @default.
- W2891333318 creator A5056378958 @default.
- W2891333318 creator A5077414771 @default.
- W2891333318 creator A5087390759 @default.
- W2891333318 date "2018-09-01" @default.
- W2891333318 modified "2023-10-14" @default.
- W2891333318 title "Long noncoding RNA SNHG6 promotes the progression of colorectal cancer through sponging miR-760 and activation of FOXC1" @default.
- W2891333318 cites W1969037652 @default.
- W2891333318 cites W1970741980 @default.
- W2891333318 cites W1973640772 @default.
- W2891333318 cites W1976550982 @default.
- W2891333318 cites W1987061720 @default.
- W2891333318 cites W1990895545 @default.
- W2891333318 cites W1993749140 @default.
- W2891333318 cites W2000865770 @default.
- W2891333318 cites W2001135054 @default.
- W2891333318 cites W2002995168 @default.
- W2891333318 cites W2046387002 @default.
- W2891333318 cites W2047717400 @default.
- W2891333318 cites W2048984063 @default.
- W2891333318 cites W2049621625 @default.
- W2891333318 cites W2070777085 @default.
- W2891333318 cites W2083557513 @default.
- W2891333318 cites W2101493293 @default.
- W2891333318 cites W2101920478 @default.
- W2891333318 cites W2324728011 @default.
- W2891333318 cites W2325443151 @default.
- W2891333318 cites W2332456247 @default.
- W2891333318 cites W2400832891 @default.
- W2891333318 cites W2484161709 @default.
- W2891333318 cites W2529101375 @default.
- W2891333318 cites W2531674656 @default.
- W2891333318 cites W2586820110 @default.
- W2891333318 cites W2597632520 @default.
- W2891333318 cites W2729932514 @default.
- W2891333318 cites W2755875138 @default.
- W2891333318 cites W2781777569 @default.
- W2891333318 doi "https://doi.org/10.2147/ott.s170246" @default.
- W2891333318 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6140718" @default.
- W2891333318 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30254467" @default.
- W2891333318 hasPublicationYear "2018" @default.
- W2891333318 type Work @default.
- W2891333318 sameAs 2891333318 @default.
- W2891333318 citedByCount "35" @default.
- W2891333318 countsByYear W28913333182018 @default.
- W2891333318 countsByYear W28913333182019 @default.
- W2891333318 countsByYear W28913333182020 @default.
- W2891333318 countsByYear W28913333182021 @default.
- W2891333318 countsByYear W28913333182022 @default.
- W2891333318 countsByYear W28913333182023 @default.
- W2891333318 crossrefType "journal-article" @default.
- W2891333318 hasAuthorship W2891333318A5002577443 @default.
- W2891333318 hasAuthorship W2891333318A5035687873 @default.
- W2891333318 hasAuthorship W2891333318A5050602839 @default.
- W2891333318 hasAuthorship W2891333318A5056378958 @default.
- W2891333318 hasAuthorship W2891333318A5077414771 @default.
- W2891333318 hasAuthorship W2891333318A5087390759 @default.
- W2891333318 hasBestOaLocation W28913333181 @default.
- W2891333318 hasConcept C104317684 @default.
- W2891333318 hasConcept C121608353 @default.
- W2891333318 hasConcept C126322002 @default.
- W2891333318 hasConcept C127561419 @default.
- W2891333318 hasConcept C173396325 @default.
- W2891333318 hasConcept C207001950 @default.
- W2891333318 hasConcept C502942594 @default.
- W2891333318 hasConcept C526805850 @default.
- W2891333318 hasConcept C54355233 @default.
- W2891333318 hasConcept C62203573 @default.
- W2891333318 hasConcept C71924100 @default.
- W2891333318 hasConcept C81885089 @default.
- W2891333318 hasConcept C86803240 @default.
- W2891333318 hasConceptScore W2891333318C104317684 @default.
- W2891333318 hasConceptScore W2891333318C121608353 @default.
- W2891333318 hasConceptScore W2891333318C126322002 @default.
- W2891333318 hasConceptScore W2891333318C127561419 @default.
- W2891333318 hasConceptScore W2891333318C173396325 @default.
- W2891333318 hasConceptScore W2891333318C207001950 @default.
- W2891333318 hasConceptScore W2891333318C502942594 @default.
- W2891333318 hasConceptScore W2891333318C526805850 @default.
- W2891333318 hasConceptScore W2891333318C54355233 @default.
- W2891333318 hasConceptScore W2891333318C62203573 @default.
- W2891333318 hasConceptScore W2891333318C71924100 @default.
- W2891333318 hasConceptScore W2891333318C81885089 @default.
- W2891333318 hasConceptScore W2891333318C86803240 @default.
- W2891333318 hasLocation W28913333181 @default.
- W2891333318 hasLocation W28913333182 @default.
- W2891333318 hasLocation W28913333183 @default.
- W2891333318 hasLocation W28913333184 @default.
- W2891333318 hasLocation W28913333185 @default.
- W2891333318 hasOpenAccess W2891333318 @default.
- W2891333318 hasPrimaryLocation W28913333181 @default.
- W2891333318 hasRelatedWork W2014813785 @default.
- W2891333318 hasRelatedWork W2024344351 @default.
- W2891333318 hasRelatedWork W2494327966 @default.