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Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer

SIMPLE SUMMARY: Long noncoding RNAs (lncRNAs) are important regulators of cell progression or regression in gastric cancer (GC). The lncRNA LOC441461 was downregulated in TNM stage IV GC. The downregulation of LOC441461 promoted the proliferation, cell cycle progression, and metastasis of GC cells i...

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Autores principales: Lee, Sang-soo, Park, JeongMan, Oh, Sooyeon, Kwack, KyuBum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8909665/
https://www.ncbi.nlm.nih.gov/pubmed/35267457
http://dx.doi.org/10.3390/cancers14051149
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author Lee, Sang-soo
Park, JeongMan
Oh, Sooyeon
Kwack, KyuBum
author_facet Lee, Sang-soo
Park, JeongMan
Oh, Sooyeon
Kwack, KyuBum
author_sort Lee, Sang-soo
collection PubMed
description SIMPLE SUMMARY: Long noncoding RNAs (lncRNAs) are important regulators of cell progression or regression in gastric cancer (GC). The lncRNA LOC441461 was downregulated in TNM stage IV GC. The downregulation of LOC441461 promoted the proliferation, cell cycle progression, and metastasis of GC cells in vitro. We confirmed, with predictable targets, that LOC441461 interacts with transcription factors and promotes tumor progression. Our study suggests LOC441461 as a potential biomarker, which could also lead to a therapeutic target in patients with advanced TNM stage gastric cancer. ABSTRACT: Gastric cancer is a common tumor, with a high mortality rate. The severity of gastric cancer is assessed by TNM staging. Long noncoding RNAs (lncRNAs) play a role in cancer treatment; investigating the clinical significance of novel biomarkers associated with TNM staging, such as lncRNAs, is important. In this study, we investigated the association between the expression of the lncRNA LOC441461 and gastric cancer stage. LOC441461 expression was lower in stage IV than in stages I, II, and III. The depletion of LOC441461 promoted cell proliferation, cell cycle progression, apoptosis, cell motility, and invasiveness. LOC441461 downregulation increased the epithelial-to-mesenchymal transition, as indicated by increased TRAIL signaling and decreased RUNX1 interactions. The interaction of the transcription factors RELA, IRF1, ESR1, AR, POU5F1, TRIM28, and GATA1 with LOC441461 affected the degree of the malignancy of gastric cancer by modulating gene transcription. The present study identified LOC441461 and seven transcription factors as potential biomarkers and therapeutic targets for the treatment of gastric cancer.
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spelling pubmed-89096652022-03-11 Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer Lee, Sang-soo Park, JeongMan Oh, Sooyeon Kwack, KyuBum Cancers (Basel) Article SIMPLE SUMMARY: Long noncoding RNAs (lncRNAs) are important regulators of cell progression or regression in gastric cancer (GC). The lncRNA LOC441461 was downregulated in TNM stage IV GC. The downregulation of LOC441461 promoted the proliferation, cell cycle progression, and metastasis of GC cells in vitro. We confirmed, with predictable targets, that LOC441461 interacts with transcription factors and promotes tumor progression. Our study suggests LOC441461 as a potential biomarker, which could also lead to a therapeutic target in patients with advanced TNM stage gastric cancer. ABSTRACT: Gastric cancer is a common tumor, with a high mortality rate. The severity of gastric cancer is assessed by TNM staging. Long noncoding RNAs (lncRNAs) play a role in cancer treatment; investigating the clinical significance of novel biomarkers associated with TNM staging, such as lncRNAs, is important. In this study, we investigated the association between the expression of the lncRNA LOC441461 and gastric cancer stage. LOC441461 expression was lower in stage IV than in stages I, II, and III. The depletion of LOC441461 promoted cell proliferation, cell cycle progression, apoptosis, cell motility, and invasiveness. LOC441461 downregulation increased the epithelial-to-mesenchymal transition, as indicated by increased TRAIL signaling and decreased RUNX1 interactions. The interaction of the transcription factors RELA, IRF1, ESR1, AR, POU5F1, TRIM28, and GATA1 with LOC441461 affected the degree of the malignancy of gastric cancer by modulating gene transcription. The present study identified LOC441461 and seven transcription factors as potential biomarkers and therapeutic targets for the treatment of gastric cancer. MDPI 2022-02-23 /pmc/articles/PMC8909665/ /pubmed/35267457 http://dx.doi.org/10.3390/cancers14051149 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Sang-soo
Park, JeongMan
Oh, Sooyeon
Kwack, KyuBum
Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer
title Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer
title_full Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer
title_fullStr Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer
title_full_unstemmed Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer
title_short Downregulation of LOC441461 Promotes Cell Growth and Motility in Human Gastric Cancer
title_sort downregulation of loc441461 promotes cell growth and motility in human gastric cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8909665/
https://www.ncbi.nlm.nih.gov/pubmed/35267457
http://dx.doi.org/10.3390/cancers14051149
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