Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer

Abstract Background Long non-coding RNAs (LncRNAs) are a class of newly identified transcripts recognized as critical governors of gene expression during human carcinogenesis, whereas their tumor-suppressive or tumor-promoting effects on gastric cancer (GC) are required for further investigation. In...

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Main Authors: Xiongdong Zhong, Xianchang Yu, Xiaoyan Wen, Lei Chen, Ni Gu
Format: Article
Language:English
Published: BMC 2020-06-01
Series:Cancer Cell International
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12935-020-01369-7
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author Xiongdong Zhong
Xianchang Yu
Xiaoyan Wen
Lei Chen
Ni Gu
author_facet Xiongdong Zhong
Xianchang Yu
Xiaoyan Wen
Lei Chen
Ni Gu
author_sort Xiongdong Zhong
collection DOAJ
description Abstract Background Long non-coding RNAs (LncRNAs) are a class of newly identified transcripts recognized as critical governors of gene expression during human carcinogenesis, whereas their tumor-suppressive or tumor-promoting effects on gastric cancer (GC) are required for further investigation. In the study, we identify the expression pattern of a novel lncRNA LINC00242 in GC and its possible permissive role in the development of GC. Methods The study included 68 pairs of GC and adjacent normal gastric tissue samples. The viability, migration, and invasion of cultured human GC cells HGC27 were evaluated by CCK-8 and Transwell chamber assays. In vitro tube formation of human brain microvascular endothelial cells (HBMVECs) in HGC27 cell coculture was detected. The regulatory network of LINC00242/miR-141/FOXC1 was verified using dual luciferase reporter gene assay and RNA immunoprecipitation (RIP) assay. Subcutaneous xenografts of HGC27 cells were performed in nude mice. Results LINC00242 was highly expressed in GC tissues and cells and contributed to poor prognosis. LINC00242 knockdown inhibited HGC27 cell viability, migration and invasion, and tube formation of HBMVECs. LINC00242 interacted with miR-141 and positively regulated FOXC1, a target gene of miR-141. LINC00242 knockdown was partially lost in HGC27 cells upon miR-141 inhibition or FOXC1 overexpression. The tumor-promoting effect of LINC00242 on GC was demonstrated in nude mice. Conclusion Taken together, the present study demonstrates the oncogenic role of the LINC00242/miR-141/FOXC1 axis in GC, highlighting a theoretical basis for GC treatment.
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spelling doaj.art-0c3489fd9af1462a9b6846ead847f10c2022-12-22T00:23:40ZengBMCCancer Cell International1475-28672020-06-0120111110.1186/s12935-020-01369-7Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancerXiongdong Zhong0Xianchang Yu1Xiaoyan Wen2Lei Chen3Ni Gu4Department of General Surgery, Zhuhai People’s Hospital (Zhuhai hospital affiliated with Jinan University)Department of General Surgery, Zhuhai People’s Hospital (Zhuhai hospital affiliated with Jinan University)Department of General Surgery, Zhuhai People’s Hospital (Zhuhai hospital affiliated with Jinan University)Department of General Surgery, Zhuhai People’s Hospital (Zhuhai hospital affiliated with Jinan University)Department of General Surgery, Zhuhai People’s Hospital (Zhuhai hospital affiliated with Jinan University)Abstract Background Long non-coding RNAs (LncRNAs) are a class of newly identified transcripts recognized as critical governors of gene expression during human carcinogenesis, whereas their tumor-suppressive or tumor-promoting effects on gastric cancer (GC) are required for further investigation. In the study, we identify the expression pattern of a novel lncRNA LINC00242 in GC and its possible permissive role in the development of GC. Methods The study included 68 pairs of GC and adjacent normal gastric tissue samples. The viability, migration, and invasion of cultured human GC cells HGC27 were evaluated by CCK-8 and Transwell chamber assays. In vitro tube formation of human brain microvascular endothelial cells (HBMVECs) in HGC27 cell coculture was detected. The regulatory network of LINC00242/miR-141/FOXC1 was verified using dual luciferase reporter gene assay and RNA immunoprecipitation (RIP) assay. Subcutaneous xenografts of HGC27 cells were performed in nude mice. Results LINC00242 was highly expressed in GC tissues and cells and contributed to poor prognosis. LINC00242 knockdown inhibited HGC27 cell viability, migration and invasion, and tube formation of HBMVECs. LINC00242 interacted with miR-141 and positively regulated FOXC1, a target gene of miR-141. LINC00242 knockdown was partially lost in HGC27 cells upon miR-141 inhibition or FOXC1 overexpression. The tumor-promoting effect of LINC00242 on GC was demonstrated in nude mice. Conclusion Taken together, the present study demonstrates the oncogenic role of the LINC00242/miR-141/FOXC1 axis in GC, highlighting a theoretical basis for GC treatment.http://link.springer.com/article/10.1186/s12935-020-01369-7Gastric cancerLINC00242MicroRNA-141FOXC1
spellingShingle Xiongdong Zhong
Xianchang Yu
Xiaoyan Wen
Lei Chen
Ni Gu
Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer
Cancer Cell International
Gastric cancer
LINC00242
MicroRNA-141
FOXC1
title Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer
title_full Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer
title_fullStr Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer
title_full_unstemmed Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer
title_short Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer
title_sort activation of the linc00242 mir 141 foxc1 axis underpins the development of gastric cancer
topic Gastric cancer
LINC00242
MicroRNA-141
FOXC1
url http://link.springer.com/article/10.1186/s12935-020-01369-7
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AT xiaoyanwen activationofthelinc00242mir141foxc1axisunderpinsthedevelopmentofgastriccancer
AT leichen activationofthelinc00242mir141foxc1axisunderpinsthedevelopmentofgastriccancer
AT nigu activationofthelinc00242mir141foxc1axisunderpinsthedevelopmentofgastriccancer