Cargando…

Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells

Gastric cancer is one of the most common cancers and the leading causes of cancer mortality. However, the molecular mechanisms of gastric cancer malignancy remain unclear. Long noncoding RNAs (lncRNAs) have been well documented in controlling cancer progression. Identification of critical lncRNAs in...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Boya, Deng, Yujie, Jin, Juan, Wu, Yan, Shen, Lirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247385/
https://www.ncbi.nlm.nih.gov/pubmed/34234860
http://dx.doi.org/10.7150/jca.58185
_version_ 1783716513670234112
author Wang, Boya
Deng, Yujie
Jin, Juan
Wu, Yan
Shen, Lirong
author_facet Wang, Boya
Deng, Yujie
Jin, Juan
Wu, Yan
Shen, Lirong
author_sort Wang, Boya
collection PubMed
description Gastric cancer is one of the most common cancers and the leading causes of cancer mortality. However, the molecular mechanisms of gastric cancer malignancy remain unclear. Long noncoding RNAs (lncRNAs) have been well documented in controlling cancer progression. Identification of critical lncRNAs in gastric cancer will provide new sights into the regulation mechanism of gastric cancer. Here, we screened differentially expressed lncRNAs in gastric cancer tissues and matched adjacent tissues and found that lncRNA LIT3527, a 486-nucleotide (nt) sense transcript, was frequently upregulated in gastric cancer tissues. Knockdown of LIT3527 dramatically suppressed proliferation and migration of gastric cancer cells through inducing severe cell death but not affecting cell cycle. Mechanistically, we uncovered that depletion of LIT35227 induced significant cell apoptosis and autophagy through inhibiting AKT/ERK/mTOR signaling pathway. Targeting LIT3527 showed a robust inhibition of lung metastasis of gastric cancer cells. Taken together, these results suggest that LIT3527 is essential for gastric cancer cell survival through maintaining mTOR activity, suggesting that it may be clinically valuable as a therapeutic target for gastric cancer.
format Online
Article
Text
id pubmed-8247385
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-82473852021-07-06 Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells Wang, Boya Deng, Yujie Jin, Juan Wu, Yan Shen, Lirong J Cancer Research Paper Gastric cancer is one of the most common cancers and the leading causes of cancer mortality. However, the molecular mechanisms of gastric cancer malignancy remain unclear. Long noncoding RNAs (lncRNAs) have been well documented in controlling cancer progression. Identification of critical lncRNAs in gastric cancer will provide new sights into the regulation mechanism of gastric cancer. Here, we screened differentially expressed lncRNAs in gastric cancer tissues and matched adjacent tissues and found that lncRNA LIT3527, a 486-nucleotide (nt) sense transcript, was frequently upregulated in gastric cancer tissues. Knockdown of LIT3527 dramatically suppressed proliferation and migration of gastric cancer cells through inducing severe cell death but not affecting cell cycle. Mechanistically, we uncovered that depletion of LIT35227 induced significant cell apoptosis and autophagy through inhibiting AKT/ERK/mTOR signaling pathway. Targeting LIT3527 showed a robust inhibition of lung metastasis of gastric cancer cells. Taken together, these results suggest that LIT3527 is essential for gastric cancer cell survival through maintaining mTOR activity, suggesting that it may be clinically valuable as a therapeutic target for gastric cancer. Ivyspring International Publisher 2021-06-11 /pmc/articles/PMC8247385/ /pubmed/34234860 http://dx.doi.org/10.7150/jca.58185 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Boya
Deng, Yujie
Jin, Juan
Wu, Yan
Shen, Lirong
Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells
title Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells
title_full Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells
title_fullStr Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells
title_full_unstemmed Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells
title_short Long Noncoding RNA LIT3527 Knockdown induces Apoptosis and Autophagy through inhibiting mTOR pathway in Gastric Cancer Cells
title_sort long noncoding rna lit3527 knockdown induces apoptosis and autophagy through inhibiting mtor pathway in gastric cancer cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247385/
https://www.ncbi.nlm.nih.gov/pubmed/34234860
http://dx.doi.org/10.7150/jca.58185
work_keys_str_mv AT wangboya longnoncodingrnalit3527knockdowninducesapoptosisandautophagythroughinhibitingmtorpathwayingastriccancercells
AT dengyujie longnoncodingrnalit3527knockdowninducesapoptosisandautophagythroughinhibitingmtorpathwayingastriccancercells
AT jinjuan longnoncodingrnalit3527knockdowninducesapoptosisandautophagythroughinhibitingmtorpathwayingastriccancercells
AT wuyan longnoncodingrnalit3527knockdowninducesapoptosisandautophagythroughinhibitingmtorpathwayingastriccancercells
AT shenlirong longnoncodingrnalit3527knockdowninducesapoptosisandautophagythroughinhibitingmtorpathwayingastriccancercells