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The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma

BACKGROUND: Lung adenocarcinoma (LUAD) is a fatal malignancy in the world. Growing evidence demonstrated that autophagy-related genes regulated the immune cell infiltration and correlated with the prognosis of LUAD. However, the autophagy-based signature that can predict the prognosis and the effici...

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Autores principales: Li, Xizhe, Dai, Ziyu, Wu, Xianning, Zhang, Nan, Zhang, Hao, Wang, Zeyu, Zhang, Xun, Liang, Xisong, Luo, Peng, Zhang, Jian, Liu, Zaoqu, Zhou, Yanwu, Cheng, Quan, Chang, Ruimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072793/
https://www.ncbi.nlm.nih.gov/pubmed/35529878
http://dx.doi.org/10.3389/fimmu.2022.749241
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author Li, Xizhe
Dai, Ziyu
Wu, Xianning
Zhang, Nan
Zhang, Hao
Wang, Zeyu
Zhang, Xun
Liang, Xisong
Luo, Peng
Zhang, Jian
Liu, Zaoqu
Zhou, Yanwu
Cheng, Quan
Chang, Ruimin
author_facet Li, Xizhe
Dai, Ziyu
Wu, Xianning
Zhang, Nan
Zhang, Hao
Wang, Zeyu
Zhang, Xun
Liang, Xisong
Luo, Peng
Zhang, Jian
Liu, Zaoqu
Zhou, Yanwu
Cheng, Quan
Chang, Ruimin
author_sort Li, Xizhe
collection PubMed
description BACKGROUND: Lung adenocarcinoma (LUAD) is a fatal malignancy in the world. Growing evidence demonstrated that autophagy-related genes regulated the immune cell infiltration and correlated with the prognosis of LUAD. However, the autophagy-based signature that can predict the prognosis and the efficiency of checkpoint immunotherapy in LUAD patients is yet to be discovered. METHODS: We used conventional autophagy-related genes to screen candidates for signature construction in TCGA cohort and 9 GEO datasets (tumor samples, n=2181; normal samples, n=419). An autophagy-based signature was constructed, its correlation with the prognosis and the immune infiltration of LUAD patients was explored. The prognostic value of the autophagy-based signature was validated in an independent cohort with 70 LUAD patients. Single-cell sequencing data was used to further characterize the various immunological patterns in tumors with different signature levels. Moreover, the predictive value of autophagy-based signature in PD-1 immunotherapy was explored in the IMvigor210 dataset. At last, the protective role of DRAM1 in LUAD was validated by in vitro experiments. RESULTS: After screening autophagy-related gene candidates, a signature composed by CCR2, ITGB1, and DRAM1 was established with the ATscore in each sample. Further analyses showed that the ATscore was significantly associated with immune cell infiltration and low ATscore indicated poor prognosis. Meanwhile, the prognostic value of ATscore was validated in our independent LUAD cohort. GSEA analyses and single-cell sequencing analyses revealed that ATscore was associated with the immunological status of LUAD tumors, and ATscore could predict the efficacy of PD-1 immunotherapy. Moreover, in vitro experiments demonstrated that the inhibition of DRAM1 suppressed the proliferation and migration capacity of LUAD cells. CONCLUSION: Our study identified a new autophagy-based signature that can predict the prognosis of LUAD patients, and this ATscore has potential applicative value in the checkpoint therapy efficiency prediction.
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spelling pubmed-90727932022-05-07 The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma Li, Xizhe Dai, Ziyu Wu, Xianning Zhang, Nan Zhang, Hao Wang, Zeyu Zhang, Xun Liang, Xisong Luo, Peng Zhang, Jian Liu, Zaoqu Zhou, Yanwu Cheng, Quan Chang, Ruimin Front Immunol Immunology BACKGROUND: Lung adenocarcinoma (LUAD) is a fatal malignancy in the world. Growing evidence demonstrated that autophagy-related genes regulated the immune cell infiltration and correlated with the prognosis of LUAD. However, the autophagy-based signature that can predict the prognosis and the efficiency of checkpoint immunotherapy in LUAD patients is yet to be discovered. METHODS: We used conventional autophagy-related genes to screen candidates for signature construction in TCGA cohort and 9 GEO datasets (tumor samples, n=2181; normal samples, n=419). An autophagy-based signature was constructed, its correlation with the prognosis and the immune infiltration of LUAD patients was explored. The prognostic value of the autophagy-based signature was validated in an independent cohort with 70 LUAD patients. Single-cell sequencing data was used to further characterize the various immunological patterns in tumors with different signature levels. Moreover, the predictive value of autophagy-based signature in PD-1 immunotherapy was explored in the IMvigor210 dataset. At last, the protective role of DRAM1 in LUAD was validated by in vitro experiments. RESULTS: After screening autophagy-related gene candidates, a signature composed by CCR2, ITGB1, and DRAM1 was established with the ATscore in each sample. Further analyses showed that the ATscore was significantly associated with immune cell infiltration and low ATscore indicated poor prognosis. Meanwhile, the prognostic value of ATscore was validated in our independent LUAD cohort. GSEA analyses and single-cell sequencing analyses revealed that ATscore was associated with the immunological status of LUAD tumors, and ATscore could predict the efficacy of PD-1 immunotherapy. Moreover, in vitro experiments demonstrated that the inhibition of DRAM1 suppressed the proliferation and migration capacity of LUAD cells. CONCLUSION: Our study identified a new autophagy-based signature that can predict the prognosis of LUAD patients, and this ATscore has potential applicative value in the checkpoint therapy efficiency prediction. Frontiers Media S.A. 2022-04-22 /pmc/articles/PMC9072793/ /pubmed/35529878 http://dx.doi.org/10.3389/fimmu.2022.749241 Text en Copyright © 2022 Li, Dai, Wu, Zhang, Zhang, Wang, Zhang, Liang, Luo, Zhang, Liu, Zhou, Cheng and Chang 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 Immunology
Li, Xizhe
Dai, Ziyu
Wu, Xianning
Zhang, Nan
Zhang, Hao
Wang, Zeyu
Zhang, Xun
Liang, Xisong
Luo, Peng
Zhang, Jian
Liu, Zaoqu
Zhou, Yanwu
Cheng, Quan
Chang, Ruimin
The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma
title The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma
title_full The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma
title_fullStr The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma
title_full_unstemmed The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma
title_short The Comprehensive Analysis Identified an Autophagy Signature for the Prognosis and the Immunotherapy Efficiency Prediction in Lung Adenocarcinoma
title_sort comprehensive analysis identified an autophagy signature for the prognosis and the immunotherapy efficiency prediction in lung adenocarcinoma
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072793/
https://www.ncbi.nlm.nih.gov/pubmed/35529878
http://dx.doi.org/10.3389/fimmu.2022.749241
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