Cargando…

sLAG-3 in non-small-cell lung cancer patients’ serum

BACKGROUND: Anti-programmed cell death-1/programmed cell death ligand-1 monoclonal antibodies have been widely used in non-small-cell lung cancer (NSCLC), but not every patient can get benefits from them. Whether other molecular markers can predict the results of programmed cell death-1/programmed c...

Descripción completa

Detalles Bibliográficos
Autores principales: He, Yayi, Wang, Yan, Zhao, Sha, Zhao, Chao, Zhou, Caicun, Hirsch, Fred R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097502/
https://www.ncbi.nlm.nih.gov/pubmed/30147330
http://dx.doi.org/10.2147/OTT.S164178
_version_ 1783348318178377728
author He, Yayi
Wang, Yan
Zhao, Sha
Zhao, Chao
Zhou, Caicun
Hirsch, Fred R
author_facet He, Yayi
Wang, Yan
Zhao, Sha
Zhao, Chao
Zhou, Caicun
Hirsch, Fred R
author_sort He, Yayi
collection PubMed
description BACKGROUND: Anti-programmed cell death-1/programmed cell death ligand-1 monoclonal antibodies have been widely used in non-small-cell lung cancer (NSCLC), but not every patient can get benefits from them. Whether other molecular markers can predict the results of programmed cell death-1/programmed cell death ligand-1 inhibitors need to be explored. Lymphocyte-activation gene-3 (LAG-3) is another important immune checkpoint, which can inhibit tumor immunity. Soluble LAG-3 (sLAG-3) plays different functions from LAG-3. In this study, we detected the serum sLAG-3 level in NSCLC patients. METHODS: sLAG-3 was detected in 247 hospitalized patients by enzyme-linked immunosorbent assay. Every sample was repeated three times. RESULTS: Two-hundred forty-seven hospitalized patients were enrolled in this study. Of them, 71 had benign diseases and 176 were NSCLC patients. sLAG-3 in NSCLC serum was correlated with NSCLC stage. The sLAG-3 levels were significantly higher in stage I–II NSCLC than in stage III–IV (p<0.001). CONCLUSION: The advanced NSCLC had the lower sLAG-3 expression. This might be related to the poor cancer immune response. Increasing sLAG-3 level might be a promising treatment in advanced NSCLC patients.
format Online
Article
Text
id pubmed-6097502
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-60975022018-08-24 sLAG-3 in non-small-cell lung cancer patients’ serum He, Yayi Wang, Yan Zhao, Sha Zhao, Chao Zhou, Caicun Hirsch, Fred R Onco Targets Ther Original Research BACKGROUND: Anti-programmed cell death-1/programmed cell death ligand-1 monoclonal antibodies have been widely used in non-small-cell lung cancer (NSCLC), but not every patient can get benefits from them. Whether other molecular markers can predict the results of programmed cell death-1/programmed cell death ligand-1 inhibitors need to be explored. Lymphocyte-activation gene-3 (LAG-3) is another important immune checkpoint, which can inhibit tumor immunity. Soluble LAG-3 (sLAG-3) plays different functions from LAG-3. In this study, we detected the serum sLAG-3 level in NSCLC patients. METHODS: sLAG-3 was detected in 247 hospitalized patients by enzyme-linked immunosorbent assay. Every sample was repeated three times. RESULTS: Two-hundred forty-seven hospitalized patients were enrolled in this study. Of them, 71 had benign diseases and 176 were NSCLC patients. sLAG-3 in NSCLC serum was correlated with NSCLC stage. The sLAG-3 levels were significantly higher in stage I–II NSCLC than in stage III–IV (p<0.001). CONCLUSION: The advanced NSCLC had the lower sLAG-3 expression. This might be related to the poor cancer immune response. Increasing sLAG-3 level might be a promising treatment in advanced NSCLC patients. Dove Medical Press 2018-08-13 /pmc/articles/PMC6097502/ /pubmed/30147330 http://dx.doi.org/10.2147/OTT.S164178 Text en © 2018 He et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
He, Yayi
Wang, Yan
Zhao, Sha
Zhao, Chao
Zhou, Caicun
Hirsch, Fred R
sLAG-3 in non-small-cell lung cancer patients’ serum
title sLAG-3 in non-small-cell lung cancer patients’ serum
title_full sLAG-3 in non-small-cell lung cancer patients’ serum
title_fullStr sLAG-3 in non-small-cell lung cancer patients’ serum
title_full_unstemmed sLAG-3 in non-small-cell lung cancer patients’ serum
title_short sLAG-3 in non-small-cell lung cancer patients’ serum
title_sort slag-3 in non-small-cell lung cancer patients’ serum
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097502/
https://www.ncbi.nlm.nih.gov/pubmed/30147330
http://dx.doi.org/10.2147/OTT.S164178
work_keys_str_mv AT heyayi slag3innonsmallcelllungcancerpatientsserum
AT wangyan slag3innonsmallcelllungcancerpatientsserum
AT zhaosha slag3innonsmallcelllungcancerpatientsserum
AT zhaochao slag3innonsmallcelllungcancerpatientsserum
AT zhoucaicun slag3innonsmallcelllungcancerpatientsserum
AT hirschfredr slag3innonsmallcelllungcancerpatientsserum