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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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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 |
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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 |
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