Cargando…

Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation

Non–small cell lung cancer (NSCLC) is the most commonly diagnosed cancer and the leading cause of cancer death worldwide. More than half of patients with NSCLC die after developing distant metastases, so rapid, minimally invasive prognostic biomarkers are needed to reduce mortality. We used proteomi...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Yang, Fan, Jia, Xu, Ting, Ahmadinejad, Navid, Hess, Kenneth, Lin, Steven H., Zhang, Jianjun, Liu, Xi, Liu, Li, Ning, Bo, Liao, Zhongxing, Hu, Tony Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065889/
https://www.ncbi.nlm.nih.gov/pubmed/32195353
http://dx.doi.org/10.1126/sciadv.aaz6162
_version_ 1783505141921480704
author Liu, Yang
Fan, Jia
Xu, Ting
Ahmadinejad, Navid
Hess, Kenneth
Lin, Steven H.
Zhang, Jianjun
Liu, Xi
Liu, Li
Ning, Bo
Liao, Zhongxing
Hu, Tony Y.
author_facet Liu, Yang
Fan, Jia
Xu, Ting
Ahmadinejad, Navid
Hess, Kenneth
Lin, Steven H.
Zhang, Jianjun
Liu, Xi
Liu, Li
Ning, Bo
Liao, Zhongxing
Hu, Tony Y.
author_sort Liu, Yang
collection PubMed
description Non–small cell lung cancer (NSCLC) is the most commonly diagnosed cancer and the leading cause of cancer death worldwide. More than half of patients with NSCLC die after developing distant metastases, so rapid, minimally invasive prognostic biomarkers are needed to reduce mortality. We used proteomics to identify proteins differentially expressed on extracellular vesicles (EVs) of nonmetastatic 393P and metastatic 344SQ NSCLC cell lines and found that tetraspanin-8 (Tspan8) was selectively enriched on 344SQ EVs. NSCLC cell lines treated with EVs overexpressing Tspan8 also exhibited increased Matrigel invasion. Elevated Tspan8 expression on serum EVs of individuals with stage III premetastatic NSCLC tumors was also associated with reduced distant metastasis–free survival, suggesting that Tspan8 levels on serum EVs may predict future metastasis. This result suggests that a minimally invasive blood test to analyze EV expression of Tspan8 may be of potential value to guide therapeutic decisions for patients with NSCLC and merits further study.
format Online
Article
Text
id pubmed-7065889
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-70658892020-03-19 Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation Liu, Yang Fan, Jia Xu, Ting Ahmadinejad, Navid Hess, Kenneth Lin, Steven H. Zhang, Jianjun Liu, Xi Liu, Li Ning, Bo Liao, Zhongxing Hu, Tony Y. Sci Adv Research Articles Non–small cell lung cancer (NSCLC) is the most commonly diagnosed cancer and the leading cause of cancer death worldwide. More than half of patients with NSCLC die after developing distant metastases, so rapid, minimally invasive prognostic biomarkers are needed to reduce mortality. We used proteomics to identify proteins differentially expressed on extracellular vesicles (EVs) of nonmetastatic 393P and metastatic 344SQ NSCLC cell lines and found that tetraspanin-8 (Tspan8) was selectively enriched on 344SQ EVs. NSCLC cell lines treated with EVs overexpressing Tspan8 also exhibited increased Matrigel invasion. Elevated Tspan8 expression on serum EVs of individuals with stage III premetastatic NSCLC tumors was also associated with reduced distant metastasis–free survival, suggesting that Tspan8 levels on serum EVs may predict future metastasis. This result suggests that a minimally invasive blood test to analyze EV expression of Tspan8 may be of potential value to guide therapeutic decisions for patients with NSCLC and merits further study. American Association for the Advancement of Science 2020-03-11 /pmc/articles/PMC7065889/ /pubmed/32195353 http://dx.doi.org/10.1126/sciadv.aaz6162 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Liu, Yang
Fan, Jia
Xu, Ting
Ahmadinejad, Navid
Hess, Kenneth
Lin, Steven H.
Zhang, Jianjun
Liu, Xi
Liu, Li
Ning, Bo
Liao, Zhongxing
Hu, Tony Y.
Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation
title Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation
title_full Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation
title_fullStr Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation
title_full_unstemmed Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation
title_short Extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation
title_sort extracellular vesicle tetraspanin-8 level predicts distant metastasis in non–small cell lung cancer after concurrent chemoradiation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065889/
https://www.ncbi.nlm.nih.gov/pubmed/32195353
http://dx.doi.org/10.1126/sciadv.aaz6162
work_keys_str_mv AT liuyang extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT fanjia extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT xuting extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT ahmadinejadnavid extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT hesskenneth extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT linstevenh extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT zhangjianjun extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT liuxi extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT liuli extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT ningbo extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT liaozhongxing extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation
AT hutonyy extracellularvesicletetraspanin8levelpredictsdistantmetastasisinnonsmallcelllungcancerafterconcurrentchemoradiation