Upregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms

To investigate the effect of Lentinan (LNT) on lung adenocarcinoma (LUAD) cell stemness and its mechanism. In this study, we founded that LNT significantly reduce the cell proliferation, activity, migration, invasion, and stemness of LUAD cells, and promote their apoptosis compared with the control...

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Autores principales: Quan Chen, Yiming Zheng, Xia Chen, Pengfei Ge, Pengcheng Wang, Bingbing Wu
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:06fd165c08974408b0d7b95bd4f8fec72021-12-01T01:42:36ZUpregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms2234-943X10.3389/fonc.2021.778096https://doaj.org/article/06fd165c08974408b0d7b95bd4f8fec72021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fonc.2021.778096/fullhttps://doaj.org/toc/2234-943XTo investigate the effect of Lentinan (LNT) on lung adenocarcinoma (LUAD) cell stemness and its mechanism. In this study, we founded that LNT significantly reduce the cell proliferation, activity, migration, invasion, and stemness of LUAD cells, and promote their apoptosis compared with the control group in vitro. Moreover, LNT significantly inhibited the volume and weight of tumors of nude mice in vivo. At the same time, LNT can significantly up-regulate miR-216a-5p levels and reduce the protein expression of phospho-JAK2 (Y1007/1008) and phospho-STAT3 (Tyr705), thereby inhibiting the JAK2/STAT3 signaling pathway. Interfering with miR-216a-5p expression and activating the JAK2/STAT3 signaling pathway can significantly reverse LNT inhibitory effects on LUAD. Collectively, LNT can inhibit the JAK2/STAT3 signaling pathway by up-regulating miR-216a-5p, reducing stemness, and promoting LUAD cells apoptosis, then slow down LUAD occurrence and development, providing concepts and experimental foundation treating patients with LUAD.Quan ChenYiming ZhengXia ChenPengfei GePengcheng WangBingbing WuFrontiers Media S.A.articlelung adenocarcinoma (LUAD)cell stemnesslentinanmiR-216a-5pJAK2/STAT3 signaling pathwayNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENFrontiers in Oncology, Vol 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic lung adenocarcinoma (LUAD)
cell stemness
lentinan
miR-216a-5p
JAK2/STAT3 signaling pathway
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle lung adenocarcinoma (LUAD)
cell stemness
lentinan
miR-216a-5p
JAK2/STAT3 signaling pathway
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Quan Chen
Yiming Zheng
Xia Chen
Pengfei Ge
Pengcheng Wang
Bingbing Wu
Upregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms
description To investigate the effect of Lentinan (LNT) on lung adenocarcinoma (LUAD) cell stemness and its mechanism. In this study, we founded that LNT significantly reduce the cell proliferation, activity, migration, invasion, and stemness of LUAD cells, and promote their apoptosis compared with the control group in vitro. Moreover, LNT significantly inhibited the volume and weight of tumors of nude mice in vivo. At the same time, LNT can significantly up-regulate miR-216a-5p levels and reduce the protein expression of phospho-JAK2 (Y1007/1008) and phospho-STAT3 (Tyr705), thereby inhibiting the JAK2/STAT3 signaling pathway. Interfering with miR-216a-5p expression and activating the JAK2/STAT3 signaling pathway can significantly reverse LNT inhibitory effects on LUAD. Collectively, LNT can inhibit the JAK2/STAT3 signaling pathway by up-regulating miR-216a-5p, reducing stemness, and promoting LUAD cells apoptosis, then slow down LUAD occurrence and development, providing concepts and experimental foundation treating patients with LUAD.
format article
author Quan Chen
Yiming Zheng
Xia Chen
Pengfei Ge
Pengcheng Wang
Bingbing Wu
author_facet Quan Chen
Yiming Zheng
Xia Chen
Pengfei Ge
Pengcheng Wang
Bingbing Wu
author_sort Quan Chen
title Upregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms
title_short Upregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms
title_full Upregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms
title_fullStr Upregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms
title_full_unstemmed Upregulation of miR-216a-5p by Lentinan Targeted Inhibition of JAK2/STAT3 Signaling Pathway to Reduce Lung Adenocarcinoma Cell Stemness, Promote Apoptosis, and Slow Down the Lung Adenocarcinoma Mechanisms
title_sort upregulation of mir-216a-5p by lentinan targeted inhibition of jak2/stat3 signaling pathway to reduce lung adenocarcinoma cell stemness, promote apoptosis, and slow down the lung adenocarcinoma mechanisms
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/06fd165c08974408b0d7b95bd4f8fec7
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AT xiachen upregulationofmir216a5pbylentinantargetedinhibitionofjak2stat3signalingpathwaytoreducelungadenocarcinomacellstemnesspromoteapoptosisandslowdownthelungadenocarcinomamechanisms
AT pengfeige upregulationofmir216a5pbylentinantargetedinhibitionofjak2stat3signalingpathwaytoreducelungadenocarcinomacellstemnesspromoteapoptosisandslowdownthelungadenocarcinomamechanisms
AT pengchengwang upregulationofmir216a5pbylentinantargetedinhibitionofjak2stat3signalingpathwaytoreducelungadenocarcinomacellstemnesspromoteapoptosisandslowdownthelungadenocarcinomamechanisms
AT bingbingwu upregulationofmir216a5pbylentinantargetedinhibitionofjak2stat3signalingpathwaytoreducelungadenocarcinomacellstemnesspromoteapoptosisandslowdownthelungadenocarcinomamechanisms
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