Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axis

Hongyang Qi, Zhanyu Xiao, Yunxi WangDepartment of Gastroenterology, The Central Hospital of Xinxiang, Xinxiang, Henan 453000, People’s Republic of ChinaCorrespondence: Hongyang QiDepartment of Gastroenterology, The Central Hospital of Xinxiang, No. 56 Jinsui Road, Xinxiang, Henan 453000, P...

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Main Authors: Qi H, Xiao Z, Wang Y
Format: Article
Language:English
Published: Dove Medical Press 2019-08-01
Series:OncoTargets and Therapy
Subjects:
Online Access:https://www.dovepress.com/long-non-coding-rna-linc00665-gastric-cancer-tumorigenesis-by-regulati-peer-reviewed-article-OTT
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spelling doaj-db4cff8bfd55447aa8cb6ae2591752182020-11-24T21:40:25ZengDove Medical PressOncoTargets and Therapy1178-69302019-08-01Volume 126981699048197Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axisQi HXiao ZWang YHongyang Qi, Zhanyu Xiao, Yunxi WangDepartment of Gastroenterology, The Central Hospital of Xinxiang, Xinxiang, Henan 453000, People’s Republic of ChinaCorrespondence: Hongyang QiDepartment of Gastroenterology, The Central Hospital of Xinxiang, No. 56 Jinsui Road, Xinxiang, Henan 453000, People’s Republic of ChinaEmail qihongyangsun@163.comBackground: Recently, LINC00665 has been reported to be a pivotal regulator in kinds of malignancy, such as lung cancer and liver cancer. However, the functions and underlying mechanisms of LINC00665 in gastric cancer (GC) remain unclear.Materials and methods: We recruited 49 paired GC tissue to explore LINC00665 expression by qRT-PCR. In vitro function assays were used to explore the roles of LINC00665 in GC progression. Moreover, the interaction among LINC00665, miR-149-3p and RNF2 was explored by bioinformatics analysis and luciferase reporter assay.Results: In the present study, we found that LINC00665 expression was significantly elevated in GC tissues and cell lines. High LINC00665 expression was associated with TNM stage, histological grade, and poor prognosis of GC patients. Function assays showed that LINC00665 suppression significantly reduced GC cells viability and invasion ability in vitro. Mechanistic analysis showed that LINC00665 might serve as a ceRNA for miR-149-3p to regulate the expression of RNF2.Conclusion: Our current study revealed the LINC00665/miR-149-3p/RNF2 axis was involved in GC progression, providing novel insights into the treatment for GC.Keywords: gastric cancer, LINC00665, miR-149-3p, RNF2https://www.dovepress.com/long-non-coding-rna-linc00665-gastric-cancer-tumorigenesis-by-regulati-peer-reviewed-article-OTTgastric cancerLINC00665miR-149-3pRNF2
collection DOAJ
language English
format Article
sources DOAJ
author Qi H
Xiao Z
Wang Y
spellingShingle Qi H
Xiao Z
Wang Y
Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axis
OncoTargets and Therapy
gastric cancer
LINC00665
miR-149-3p
RNF2
author_facet Qi H
Xiao Z
Wang Y
author_sort Qi H
title Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axis
title_short Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axis
title_full Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axis
title_fullStr Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axis
title_full_unstemmed Long non-coding RNA LINC00665 gastric cancer tumorigenesis by regulation miR-149-3p/RNF2 axis
title_sort long non-coding rna linc00665 gastric cancer tumorigenesis by regulation mir-149-3p/rnf2 axis
publisher Dove Medical Press
series OncoTargets and Therapy
issn 1178-6930
publishDate 2019-08-01
description Hongyang Qi, Zhanyu Xiao, Yunxi WangDepartment of Gastroenterology, The Central Hospital of Xinxiang, Xinxiang, Henan 453000, People’s Republic of ChinaCorrespondence: Hongyang QiDepartment of Gastroenterology, The Central Hospital of Xinxiang, No. 56 Jinsui Road, Xinxiang, Henan 453000, People’s Republic of ChinaEmail qihongyangsun@163.comBackground: Recently, LINC00665 has been reported to be a pivotal regulator in kinds of malignancy, such as lung cancer and liver cancer. However, the functions and underlying mechanisms of LINC00665 in gastric cancer (GC) remain unclear.Materials and methods: We recruited 49 paired GC tissue to explore LINC00665 expression by qRT-PCR. In vitro function assays were used to explore the roles of LINC00665 in GC progression. Moreover, the interaction among LINC00665, miR-149-3p and RNF2 was explored by bioinformatics analysis and luciferase reporter assay.Results: In the present study, we found that LINC00665 expression was significantly elevated in GC tissues and cell lines. High LINC00665 expression was associated with TNM stage, histological grade, and poor prognosis of GC patients. Function assays showed that LINC00665 suppression significantly reduced GC cells viability and invasion ability in vitro. Mechanistic analysis showed that LINC00665 might serve as a ceRNA for miR-149-3p to regulate the expression of RNF2.Conclusion: Our current study revealed the LINC00665/miR-149-3p/RNF2 axis was involved in GC progression, providing novel insights into the treatment for GC.Keywords: gastric cancer, LINC00665, miR-149-3p, RNF2
topic gastric cancer
LINC00665
miR-149-3p
RNF2
url https://www.dovepress.com/long-non-coding-rna-linc00665-gastric-cancer-tumorigenesis-by-regulati-peer-reviewed-article-OTT
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