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LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma

LINC00675 has been suggested to be dysregulated in gastric cancer, colorectal cancer and pancreatic cancer. However, the expression status and biological function of LINC00675 in glioma were still unknown. Thus, we reported LINC00675 was overexpressed in glioma tissues and cell lines, and positively...

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Detalles Bibliográficos
Autores principales: Li, Zhibing, Li, Yijian, Wang, Qibai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146294/
https://www.ncbi.nlm.nih.gov/pubmed/30061182
http://dx.doi.org/10.1042/BSR20181039
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author Li, Zhibing
Li, Yijian
Wang, Qibai
author_facet Li, Zhibing
Li, Yijian
Wang, Qibai
author_sort Li, Zhibing
collection PubMed
description LINC00675 has been suggested to be dysregulated in gastric cancer, colorectal cancer and pancreatic cancer. However, the expression status and biological function of LINC00675 in glioma were still unknown. Thus, we reported LINC00675 was overexpressed in glioma tissues and cell lines, and positively associated with advanced WHO grade, large tumor size and poor prognosis. Moreover, univariate and multivariate analyses suggested that high-expression of LINC00675 was an independent unfavorable prognostic predictor for glioma. In addition, levels of LINC00675 expression were positively correlated with TRIP6 mRNA and protein expressions. The in vitro experiment showed that silencing of LINC00675 inhibits glioma cell proliferation, migration and invasion through regulating TRIP6. In conclusion, LINC00675 acts as a tumor promoter in glioma progression.
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spelling pubmed-61462942018-09-25 LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma Li, Zhibing Li, Yijian Wang, Qibai Biosci Rep Research Articles LINC00675 has been suggested to be dysregulated in gastric cancer, colorectal cancer and pancreatic cancer. However, the expression status and biological function of LINC00675 in glioma were still unknown. Thus, we reported LINC00675 was overexpressed in glioma tissues and cell lines, and positively associated with advanced WHO grade, large tumor size and poor prognosis. Moreover, univariate and multivariate analyses suggested that high-expression of LINC00675 was an independent unfavorable prognostic predictor for glioma. In addition, levels of LINC00675 expression were positively correlated with TRIP6 mRNA and protein expressions. The in vitro experiment showed that silencing of LINC00675 inhibits glioma cell proliferation, migration and invasion through regulating TRIP6. In conclusion, LINC00675 acts as a tumor promoter in glioma progression. Portland Press Ltd. 2018-09-19 /pmc/articles/PMC6146294/ /pubmed/30061182 http://dx.doi.org/10.1042/BSR20181039 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Li, Zhibing
Li, Yijian
Wang, Qibai
LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma
title LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma
title_full LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma
title_fullStr LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma
title_full_unstemmed LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma
title_short LINC00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma
title_sort linc00675 is a prognostic factor and regulates cell proliferation, migration and invasion in glioma
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146294/
https://www.ncbi.nlm.nih.gov/pubmed/30061182
http://dx.doi.org/10.1042/BSR20181039
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