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Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer
INTRODUCTION: Immune-based and antibody-drug conjugate therapies have shown promise in the treatment of patients with small cell lung cancer (SCLC). However, better predictive biomarkers are needed for selection of the appropriate SCLC patients for these advanced therapies and also for evaluation of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877464/ https://www.ncbi.nlm.nih.gov/pubmed/31819500 http://dx.doi.org/10.2147/OTT.S216362 |
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author | Regzedmaa, Orgilmaa Li, Ying Li, Yongwen Zhang, Hongbing Wang, Jin Gong, Hao Yuan, Yin Li, Weiting Liu, Hongyu Chen, Jun |
author_facet | Regzedmaa, Orgilmaa Li, Ying Li, Yongwen Zhang, Hongbing Wang, Jin Gong, Hao Yuan, Yin Li, Weiting Liu, Hongyu Chen, Jun |
author_sort | Regzedmaa, Orgilmaa |
collection | PubMed |
description | INTRODUCTION: Immune-based and antibody-drug conjugate therapies have shown promise in the treatment of patients with small cell lung cancer (SCLC). However, better predictive biomarkers are needed for selection of the appropriate SCLC patients for these advanced therapies and also for evaluation of the efficacy of these treatments. OBJECTIVE: The aim of this study was to examine the expression of delta-like protein 3 (DLL3), cytotoxic T lymphocyte-associated protein 4 (CTLA-4), and mesothelin (MSTN) in patients with SCLC and compare them with those patients’ clinical characteristics. METHODS: Immunohistochemical analyses of DLL3, CTLA-4 and MSTN expression were performed in 38 samples from patients with SCLC. RESULTS: We found that positive expression in patients of the biomarkers was as follows: for DLL3, 100% (38/38), for CTLA-4, 89.5% (36/38) and for MSTN 81.5% (31/38). The median survival time was 17.9 months in the DLL3 high expression group and 23 months in the DLL3 low expression group. Patients with a high expression of DLL3 showed a poorer prognosis than those with a low expression of DLL3 (HR=3.4; 95% CI, 1.34–8.6; p=0.01). CONCLUSION: The expression of DLL3, CTLA-4 and MSTN was not correlated with patients’ age, sex, smoking status, stage, and tumor metastasis. The fact that there was a higher expression of DLL3, CTLA-4, and MSTN in SCLC suggested that these molecules could be used as predictive biomarkers for SCLC. |
format | Online Article Text |
id | pubmed-6877464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-68774642019-12-09 Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer Regzedmaa, Orgilmaa Li, Ying Li, Yongwen Zhang, Hongbing Wang, Jin Gong, Hao Yuan, Yin Li, Weiting Liu, Hongyu Chen, Jun Onco Targets Ther Original Research INTRODUCTION: Immune-based and antibody-drug conjugate therapies have shown promise in the treatment of patients with small cell lung cancer (SCLC). However, better predictive biomarkers are needed for selection of the appropriate SCLC patients for these advanced therapies and also for evaluation of the efficacy of these treatments. OBJECTIVE: The aim of this study was to examine the expression of delta-like protein 3 (DLL3), cytotoxic T lymphocyte-associated protein 4 (CTLA-4), and mesothelin (MSTN) in patients with SCLC and compare them with those patients’ clinical characteristics. METHODS: Immunohistochemical analyses of DLL3, CTLA-4 and MSTN expression were performed in 38 samples from patients with SCLC. RESULTS: We found that positive expression in patients of the biomarkers was as follows: for DLL3, 100% (38/38), for CTLA-4, 89.5% (36/38) and for MSTN 81.5% (31/38). The median survival time was 17.9 months in the DLL3 high expression group and 23 months in the DLL3 low expression group. Patients with a high expression of DLL3 showed a poorer prognosis than those with a low expression of DLL3 (HR=3.4; 95% CI, 1.34–8.6; p=0.01). CONCLUSION: The expression of DLL3, CTLA-4 and MSTN was not correlated with patients’ age, sex, smoking status, stage, and tumor metastasis. The fact that there was a higher expression of DLL3, CTLA-4, and MSTN in SCLC suggested that these molecules could be used as predictive biomarkers for SCLC. Dove 2019-11-21 /pmc/articles/PMC6877464/ /pubmed/31819500 http://dx.doi.org/10.2147/OTT.S216362 Text en © 2019 Regzedmaa et al. http://creativecommons.org/licenses/by-nc/3.0/ 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Regzedmaa, Orgilmaa Li, Ying Li, Yongwen Zhang, Hongbing Wang, Jin Gong, Hao Yuan, Yin Li, Weiting Liu, Hongyu Chen, Jun Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer |
title | Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer |
title_full | Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer |
title_fullStr | Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer |
title_full_unstemmed | Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer |
title_short | Prevalence of DLL3, CTLA-4 and MSTN Expression in Patients with Small Cell Lung Cancer |
title_sort | prevalence of dll3, ctla-4 and mstn expression in patients with small cell lung cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877464/ https://www.ncbi.nlm.nih.gov/pubmed/31819500 http://dx.doi.org/10.2147/OTT.S216362 |
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