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Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma
BACKGROUND: Patients with advanced thyroid carcinoma (TC), such as anaplastic thyroid carcinoma (ATC), poorly differentiated thyroid carcinoma (PDTC), and locally advanced papillary thyroid carcinoma (PTC), have poor prognoses and require novel treatments. Immune checkpoint (ICP) inhibitors have dem...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094437/ https://www.ncbi.nlm.nih.gov/pubmed/35574031 http://dx.doi.org/10.3389/fendo.2022.859013 |
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author | Luo, Yi Yang, Yi-Chen Shen, Cen-Kai Ma, Ben Xu, Wei-Bo Wang, Qi-Feng Zhang, Yan Liao, Tian Wei, Wen-Jun Wang, Yu |
author_facet | Luo, Yi Yang, Yi-Chen Shen, Cen-Kai Ma, Ben Xu, Wei-Bo Wang, Qi-Feng Zhang, Yan Liao, Tian Wei, Wen-Jun Wang, Yu |
author_sort | Luo, Yi |
collection | PubMed |
description | BACKGROUND: Patients with advanced thyroid carcinoma (TC), such as anaplastic thyroid carcinoma (ATC), poorly differentiated thyroid carcinoma (PDTC), and locally advanced papillary thyroid carcinoma (PTC), have poor prognoses and require novel treatments. Immune checkpoint (ICP) inhibitors have demonstrated encouraging and good results; nevertheless, their effect in advanced TCs remains largely unclear. Thus, we demonstrated ICP profiles and investigated their potential clinical significance. METHODS: A total of 234 TC patients were involved, with 22 ATCs, 44 PDTCs, and 168 PTCs, including 58 advanced PTCs. Immunohistochemistry was performed to evaluate nine ICPs [programmed cell death ligand 1 (PDL1), Programmed cell death 1 (PD1), cytotoxic T lymphocyte-associated protein 4 (CTLA4), B and T lymphocyte attenuator (BTLA), T-cell immunoglobulin and immunoreceptor tyrosine-based inhibitory motif (ITIM) domain (TIGIT), lymphocyte activation gene 3 (LAG3), V-domain immunoglobulin suppressor of T-cell activation (VISTA), B7 homolog 3 (B7-H3), and T-cell immunoglobulin and mucin domain- 3 protein (TIM3)] expression via tissue microarrays (TMAs), and clinical correlations were analyzed simultaneously. RESULTS: ATC had the highest positive rate of ICPs among the three pathological types, as well as relatively high ICP co-expression. ATC with high expression of PDL1 positivity had a poor prognosis. Shorter survival was associated with VISTA, B7H3, TIM3, and TIGIT expression in PDTC. The greater the co-expression of these four ICPs, the poorer the prognosis in PDTC patients. VISTA and B7H3 were the two most commonly expressed ICPs in advanced PTC, both of which were linked to a poor prognosis. CONCLUSIONS: PDL1 is linked to the overall survival (OS) of ATC. A subset of PDTC is likely immunogenic with poor prognosis and co-expression of VISTA, B7H3, TIM3, and TIGIT. Furthermore, VISTA and B7H3 are prognostic biomarkers in advanced PTC. Single or combined blockade targeting these ICPs might be effective for advanced TCs in the future. |
format | Online Article Text |
id | pubmed-9094437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90944372022-05-12 Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma Luo, Yi Yang, Yi-Chen Shen, Cen-Kai Ma, Ben Xu, Wei-Bo Wang, Qi-Feng Zhang, Yan Liao, Tian Wei, Wen-Jun Wang, Yu Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Patients with advanced thyroid carcinoma (TC), such as anaplastic thyroid carcinoma (ATC), poorly differentiated thyroid carcinoma (PDTC), and locally advanced papillary thyroid carcinoma (PTC), have poor prognoses and require novel treatments. Immune checkpoint (ICP) inhibitors have demonstrated encouraging and good results; nevertheless, their effect in advanced TCs remains largely unclear. Thus, we demonstrated ICP profiles and investigated their potential clinical significance. METHODS: A total of 234 TC patients were involved, with 22 ATCs, 44 PDTCs, and 168 PTCs, including 58 advanced PTCs. Immunohistochemistry was performed to evaluate nine ICPs [programmed cell death ligand 1 (PDL1), Programmed cell death 1 (PD1), cytotoxic T lymphocyte-associated protein 4 (CTLA4), B and T lymphocyte attenuator (BTLA), T-cell immunoglobulin and immunoreceptor tyrosine-based inhibitory motif (ITIM) domain (TIGIT), lymphocyte activation gene 3 (LAG3), V-domain immunoglobulin suppressor of T-cell activation (VISTA), B7 homolog 3 (B7-H3), and T-cell immunoglobulin and mucin domain- 3 protein (TIM3)] expression via tissue microarrays (TMAs), and clinical correlations were analyzed simultaneously. RESULTS: ATC had the highest positive rate of ICPs among the three pathological types, as well as relatively high ICP co-expression. ATC with high expression of PDL1 positivity had a poor prognosis. Shorter survival was associated with VISTA, B7H3, TIM3, and TIGIT expression in PDTC. The greater the co-expression of these four ICPs, the poorer the prognosis in PDTC patients. VISTA and B7H3 were the two most commonly expressed ICPs in advanced PTC, both of which were linked to a poor prognosis. CONCLUSIONS: PDL1 is linked to the overall survival (OS) of ATC. A subset of PDTC is likely immunogenic with poor prognosis and co-expression of VISTA, B7H3, TIM3, and TIGIT. Furthermore, VISTA and B7H3 are prognostic biomarkers in advanced PTC. Single or combined blockade targeting these ICPs might be effective for advanced TCs in the future. Frontiers Media S.A. 2022-04-27 /pmc/articles/PMC9094437/ /pubmed/35574031 http://dx.doi.org/10.3389/fendo.2022.859013 Text en Copyright © 2022 Luo, Yang, Shen, Ma, Xu, Wang, Zhang, Liao, Wei and Wang https://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 | Endocrinology Luo, Yi Yang, Yi-Chen Shen, Cen-Kai Ma, Ben Xu, Wei-Bo Wang, Qi-Feng Zhang, Yan Liao, Tian Wei, Wen-Jun Wang, Yu Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma |
title | Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma |
title_full | Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma |
title_fullStr | Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma |
title_full_unstemmed | Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma |
title_short | Immune Checkpoint Protein Expression Defines the Prognosis of Advanced Thyroid Carcinoma |
title_sort | immune checkpoint protein expression defines the prognosis of advanced thyroid carcinoma |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094437/ https://www.ncbi.nlm.nih.gov/pubmed/35574031 http://dx.doi.org/10.3389/fendo.2022.859013 |
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