LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung Cancer

Non-small-cell lung carcinoma (NSCLC) is considered to be a fatal disease and characterized by a poor prognosis. Long non-coding RNAs (lncRNAs) have been reported to act as biomarkers and therapeutic targets in solid tumors. However, the expression of lncRNAs and their clinical relevance in NSCLC re...

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Main Authors: Dexin Jia, Ying Xing, Yuning Zhan, Mengru Cao, Fanglin Tian, Weina Fan, Jian Huang, Yimeng Cui, Ruixue Gu, Yaowen Cui, Yuechao Liu, Shuai Zhang, Li Cai, Xiaomei Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2021.686975/full
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spelling doaj-ffb50526da4f421b899b300def9128f22021-05-28T09:54:48ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-05-01910.3389/fcell.2021.686975686975LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung CancerDexin Jia0Ying Xing1Yuning Zhan2Mengru Cao3Fanglin Tian4Weina Fan5Jian Huang6Yimeng Cui7Ruixue Gu8Yaowen Cui9Yuechao Liu10Shuai Zhang11Li Cai12Xiaomei Li13The Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, ChinaDepartment of Pathology, Harbin Medical University Cancer Hospital, Harbin, ChinaNon-small-cell lung carcinoma (NSCLC) is considered to be a fatal disease and characterized by a poor prognosis. Long non-coding RNAs (lncRNAs) have been reported to act as biomarkers and therapeutic targets in solid tumors. However, the expression of lncRNAs and their clinical relevance in NSCLC remain undetermined. The gene expression data profiled in The Cancer Genome Atlas and Gene Expression Omnibus (GSE81089) were employed to screen differentially expressed lncRNAs in NSCLC. LINC02678 was found to be upregulated in NSCLC and exhibited hypomethylation of the promoter region in NSCLC tissues. LINC02678 (also called RP11-336A10.5) was associated with poorer overall survival and relapse-free survival in NSCLC patients. In vitro models of gain- and loss-of-function demonstrated that LINC02678 promotes NSCLC progression by promoting NSCLC cell proliferation and cell cycle progression, as well as inducing NSCLC cell migration, invasion and epithelial-mesenchymal transition. LINC02678 was primarily located in the nucleus and could bind with the enhancer of zeste homolog 2 (EZH2). Moreover, we found that LINC02678 knockdown impaired the occupancy capacity of EZH2 and trimethylation of lysine 27 on histone 3 (H3K27me3) at the promoter region of cyclin dependent kinase inhibitor 1B (CDKN1B) and E-cadherin, as confirmed by ChIP-qPCR. A mouse transplantation model further demonstrated that LINC02678 could promote the tumorigenic and metastatic capacities of NSCLC cells. We identified LINC02678 as a tumor promoter in NSCLC, which enhanced the growth and metastasis of NSCLC cells by binding with EZH2, indicating that LINC02678 may serve as a potential biomarker for cancer diagnosis and treatment.https://www.frontiersin.org/articles/10.3389/fcell.2021.686975/fullLINC02678enhancer of zeste homolog 2non-small-cell lung cancerproliferationepithelial-mesenchymal transition
collection DOAJ
language English
format Article
sources DOAJ
author Dexin Jia
Ying Xing
Yuning Zhan
Mengru Cao
Fanglin Tian
Weina Fan
Jian Huang
Yimeng Cui
Ruixue Gu
Yaowen Cui
Yuechao Liu
Shuai Zhang
Li Cai
Xiaomei Li
spellingShingle Dexin Jia
Ying Xing
Yuning Zhan
Mengru Cao
Fanglin Tian
Weina Fan
Jian Huang
Yimeng Cui
Ruixue Gu
Yaowen Cui
Yuechao Liu
Shuai Zhang
Li Cai
Xiaomei Li
LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung Cancer
Frontiers in Cell and Developmental Biology
LINC02678
enhancer of zeste homolog 2
non-small-cell lung cancer
proliferation
epithelial-mesenchymal transition
author_facet Dexin Jia
Ying Xing
Yuning Zhan
Mengru Cao
Fanglin Tian
Weina Fan
Jian Huang
Yimeng Cui
Ruixue Gu
Yaowen Cui
Yuechao Liu
Shuai Zhang
Li Cai
Xiaomei Li
author_sort Dexin Jia
title LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung Cancer
title_short LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung Cancer
title_full LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung Cancer
title_fullStr LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung Cancer
title_full_unstemmed LINC02678 as a Novel Prognostic Marker Promotes Aggressive Non-small-cell Lung Cancer
title_sort linc02678 as a novel prognostic marker promotes aggressive non-small-cell lung cancer
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-05-01
description Non-small-cell lung carcinoma (NSCLC) is considered to be a fatal disease and characterized by a poor prognosis. Long non-coding RNAs (lncRNAs) have been reported to act as biomarkers and therapeutic targets in solid tumors. However, the expression of lncRNAs and their clinical relevance in NSCLC remain undetermined. The gene expression data profiled in The Cancer Genome Atlas and Gene Expression Omnibus (GSE81089) were employed to screen differentially expressed lncRNAs in NSCLC. LINC02678 was found to be upregulated in NSCLC and exhibited hypomethylation of the promoter region in NSCLC tissues. LINC02678 (also called RP11-336A10.5) was associated with poorer overall survival and relapse-free survival in NSCLC patients. In vitro models of gain- and loss-of-function demonstrated that LINC02678 promotes NSCLC progression by promoting NSCLC cell proliferation and cell cycle progression, as well as inducing NSCLC cell migration, invasion and epithelial-mesenchymal transition. LINC02678 was primarily located in the nucleus and could bind with the enhancer of zeste homolog 2 (EZH2). Moreover, we found that LINC02678 knockdown impaired the occupancy capacity of EZH2 and trimethylation of lysine 27 on histone 3 (H3K27me3) at the promoter region of cyclin dependent kinase inhibitor 1B (CDKN1B) and E-cadherin, as confirmed by ChIP-qPCR. A mouse transplantation model further demonstrated that LINC02678 could promote the tumorigenic and metastatic capacities of NSCLC cells. We identified LINC02678 as a tumor promoter in NSCLC, which enhanced the growth and metastasis of NSCLC cells by binding with EZH2, indicating that LINC02678 may serve as a potential biomarker for cancer diagnosis and treatment.
topic LINC02678
enhancer of zeste homolog 2
non-small-cell lung cancer
proliferation
epithelial-mesenchymal transition
url https://www.frontiersin.org/articles/10.3389/fcell.2021.686975/full
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