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HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC

Currently, non-small cell lung carcinoma (NSCLC) is a major worldwide health problem. Meanwhile accumulating evidence indicates that histone deacetylase (HDAC) activation could induce PD-L1 expression in various types of cancer, especially in myeloma and B-cell lymphomas. Therefore, we hypothesized...

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Autores principales: Liu, Xiaomei, Wang, Yuxi, Zhang, Rong, Jin, Ting, Qu, Liangliang, Jin, Qianwen, Zheng, Jiasu, Sun, Jiaqi, Wu, Ziqing, Wang, Linxi, Liu, Tianxu, Zhang, Yinxu, Meng, Xiao, Wang, Ying, Wei, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186423/
https://www.ncbi.nlm.nih.gov/pubmed/32373519
http://dx.doi.org/10.3389/fonc.2020.00485
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author Liu, Xiaomei
Wang, Yuxi
Zhang, Rong
Jin, Ting
Qu, Liangliang
Jin, Qianwen
Zheng, Jiasu
Sun, Jiaqi
Wu, Ziqing
Wang, Linxi
Liu, Tianxu
Zhang, Yinxu
Meng, Xiao
Wang, Ying
Wei, Ning
author_facet Liu, Xiaomei
Wang, Yuxi
Zhang, Rong
Jin, Ting
Qu, Liangliang
Jin, Qianwen
Zheng, Jiasu
Sun, Jiaqi
Wu, Ziqing
Wang, Linxi
Liu, Tianxu
Zhang, Yinxu
Meng, Xiao
Wang, Ying
Wei, Ning
author_sort Liu, Xiaomei
collection PubMed
description Currently, non-small cell lung carcinoma (NSCLC) is a major worldwide health problem. Meanwhile accumulating evidence indicates that histone deacetylase (HDAC) activation could induce PD-L1 expression in various types of cancer, especially in myeloma and B-cell lymphomas. Therefore, we hypothesized that high-level expression of HDAC10 is associated with PD-L1 induction and poor prognosis in patients with NSCLC. In total 180 NSCLC patients receiving complete pulmonary resection and systematic lymph node dissection were enrolled from April 2004 to August 2009. The patients with integrated clinicopathological records were followed up. The expression level of HDAC10 and PD-L1 in tissue samples was determined by immunohistochemistry. We observed that HDAC10 expression in lung cancer tissue is significantly higher than that in corresponding para-cancer tissue. Moreover, HDAC10 expression positively correlated with the expression level of PD-L1 (r = 0.213, P < 0.05) in NSCLC patients. Subgroup, multivariate analysis showed that the expression level of HDAC10 can be an independent prognostic factor and high-level expression of HDAC10 indicated poor overall survival for pulmonary carcinoma (r = 0.540, P < 0.001). Our findings suggest that the expression level of HDAC10 is positively associated with PD-L1 expression and may predict the outcome of patients with NSCLC.
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spelling pubmed-71864232020-05-05 HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC Liu, Xiaomei Wang, Yuxi Zhang, Rong Jin, Ting Qu, Liangliang Jin, Qianwen Zheng, Jiasu Sun, Jiaqi Wu, Ziqing Wang, Linxi Liu, Tianxu Zhang, Yinxu Meng, Xiao Wang, Ying Wei, Ning Front Oncol Oncology Currently, non-small cell lung carcinoma (NSCLC) is a major worldwide health problem. Meanwhile accumulating evidence indicates that histone deacetylase (HDAC) activation could induce PD-L1 expression in various types of cancer, especially in myeloma and B-cell lymphomas. Therefore, we hypothesized that high-level expression of HDAC10 is associated with PD-L1 induction and poor prognosis in patients with NSCLC. In total 180 NSCLC patients receiving complete pulmonary resection and systematic lymph node dissection were enrolled from April 2004 to August 2009. The patients with integrated clinicopathological records were followed up. The expression level of HDAC10 and PD-L1 in tissue samples was determined by immunohistochemistry. We observed that HDAC10 expression in lung cancer tissue is significantly higher than that in corresponding para-cancer tissue. Moreover, HDAC10 expression positively correlated with the expression level of PD-L1 (r = 0.213, P < 0.05) in NSCLC patients. Subgroup, multivariate analysis showed that the expression level of HDAC10 can be an independent prognostic factor and high-level expression of HDAC10 indicated poor overall survival for pulmonary carcinoma (r = 0.540, P < 0.001). Our findings suggest that the expression level of HDAC10 is positively associated with PD-L1 expression and may predict the outcome of patients with NSCLC. Frontiers Media S.A. 2020-04-21 /pmc/articles/PMC7186423/ /pubmed/32373519 http://dx.doi.org/10.3389/fonc.2020.00485 Text en Copyright © 2020 Liu, Wang, Zhang, Jin, Qu, Jin, Zheng, Sun, Wu, Wang, Liu, Zhang, Meng, Wang and Wei. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Liu, Xiaomei
Wang, Yuxi
Zhang, Rong
Jin, Ting
Qu, Liangliang
Jin, Qianwen
Zheng, Jiasu
Sun, Jiaqi
Wu, Ziqing
Wang, Linxi
Liu, Tianxu
Zhang, Yinxu
Meng, Xiao
Wang, Ying
Wei, Ning
HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC
title HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC
title_full HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC
title_fullStr HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC
title_full_unstemmed HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC
title_short HDAC10 Is Positively Associated With PD-L1 Expression and Poor Prognosis in Patients With NSCLC
title_sort hdac10 is positively associated with pd-l1 expression and poor prognosis in patients with nsclc
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186423/
https://www.ncbi.nlm.nih.gov/pubmed/32373519
http://dx.doi.org/10.3389/fonc.2020.00485
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