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Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients

BACKGROUND: Young lung cancer as a small subgroup of lung cancer has not been fully studied. Most of the previous studies focused on the clinicopathological features, but studies of molecular characteristics are still few and limited. Here, we explore the characteristics of prognosis and variation i...

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Autores principales: Hu, Mingming, Tan, Jinjing, Liu, Zhentian, Li, Lifeng, Zhang, Hongmei, Zhao, Dan, Li, Baolan, Gao, Xuan, Che, Nanying, Zhang, Tongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789686/
https://www.ncbi.nlm.nih.gov/pubmed/35096611
http://dx.doi.org/10.3389/fonc.2021.806845
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author Hu, Mingming
Tan, Jinjing
Liu, Zhentian
Li, Lifeng
Zhang, Hongmei
Zhao, Dan
Li, Baolan
Gao, Xuan
Che, Nanying
Zhang, Tongmei
author_facet Hu, Mingming
Tan, Jinjing
Liu, Zhentian
Li, Lifeng
Zhang, Hongmei
Zhao, Dan
Li, Baolan
Gao, Xuan
Che, Nanying
Zhang, Tongmei
author_sort Hu, Mingming
collection PubMed
description BACKGROUND: Young lung cancer as a small subgroup of lung cancer has not been fully studied. Most of the previous studies focused on the clinicopathological features, but studies of molecular characteristics are still few and limited. Here, we explore the characteristics of prognosis and variation in young lung cancer patients with NSCLC. METHODS: A total of 5639 young lung cancer samples (NSCLC, age ≤40) were screened from the SEER and the same number of the old (NSCLC, age ≥60) were screened by propensity score matching to evaluate the prognosis of two groups. 165 treatment-naïve patients diagnosed with NSCLC were enrolled to explore the molecular feature difference between two age-varying groups. CCLE cell line expression data was used to verify the finding from the cohort of 165 patients. RESULTS: The overall survival of the young lung cancer group was significantly better than the old. Germline analysis showed a trend that the young group contained a higher incidence of germline alterations. The TMB of the young group was lower. Meanwhile, the heterogeneity and evolutionary degrees of the young lung cancer group were also lower than the old. The mutation spectrums of two groups exhibited variance with LRP1B, SMARCA4, STK11, FAT2, RBM10, FANCM mutations, EGFR L858R more recurrent in the old group and EML4-ALK fusions, BCL2L11 deletion polymorphism, EGFR 19DEL, 20IN more recurrent in the young group. For the base substitution, the young showed a lower fraction of transversion. Further, we performed a pathway analysis and found the EGFR tyrosine kinase inhibitor resistance pathway enriched in the young lung cancer group, which was validated in gene expression data later. CONCLUSIONS: There were significantly different molecular features of the young lung cancer group. The young lung cancer group had a more simple alteration structure. Alteration spectrums and base substitution types varied between two groups, implying the different pathogenesis. The young lung cancer group had more potential treatment choices. Although young lung patients had better outcomes, there were still adverse factors of them, suggesting that the young group still needs more caution for treatment choice and monitoring after the treatment to further improve the prognosis.
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spelling pubmed-87896862022-01-27 Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients Hu, Mingming Tan, Jinjing Liu, Zhentian Li, Lifeng Zhang, Hongmei Zhao, Dan Li, Baolan Gao, Xuan Che, Nanying Zhang, Tongmei Front Oncol Oncology BACKGROUND: Young lung cancer as a small subgroup of lung cancer has not been fully studied. Most of the previous studies focused on the clinicopathological features, but studies of molecular characteristics are still few and limited. Here, we explore the characteristics of prognosis and variation in young lung cancer patients with NSCLC. METHODS: A total of 5639 young lung cancer samples (NSCLC, age ≤40) were screened from the SEER and the same number of the old (NSCLC, age ≥60) were screened by propensity score matching to evaluate the prognosis of two groups. 165 treatment-naïve patients diagnosed with NSCLC were enrolled to explore the molecular feature difference between two age-varying groups. CCLE cell line expression data was used to verify the finding from the cohort of 165 patients. RESULTS: The overall survival of the young lung cancer group was significantly better than the old. Germline analysis showed a trend that the young group contained a higher incidence of germline alterations. The TMB of the young group was lower. Meanwhile, the heterogeneity and evolutionary degrees of the young lung cancer group were also lower than the old. The mutation spectrums of two groups exhibited variance with LRP1B, SMARCA4, STK11, FAT2, RBM10, FANCM mutations, EGFR L858R more recurrent in the old group and EML4-ALK fusions, BCL2L11 deletion polymorphism, EGFR 19DEL, 20IN more recurrent in the young group. For the base substitution, the young showed a lower fraction of transversion. Further, we performed a pathway analysis and found the EGFR tyrosine kinase inhibitor resistance pathway enriched in the young lung cancer group, which was validated in gene expression data later. CONCLUSIONS: There were significantly different molecular features of the young lung cancer group. The young lung cancer group had a more simple alteration structure. Alteration spectrums and base substitution types varied between two groups, implying the different pathogenesis. The young lung cancer group had more potential treatment choices. Although young lung patients had better outcomes, there were still adverse factors of them, suggesting that the young group still needs more caution for treatment choice and monitoring after the treatment to further improve the prognosis. Frontiers Media S.A. 2022-01-12 /pmc/articles/PMC8789686/ /pubmed/35096611 http://dx.doi.org/10.3389/fonc.2021.806845 Text en Copyright © 2022 Hu, Tan, Liu, Li, Zhang, Zhao, Li, Gao, Che and Zhang 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 Oncology
Hu, Mingming
Tan, Jinjing
Liu, Zhentian
Li, Lifeng
Zhang, Hongmei
Zhao, Dan
Li, Baolan
Gao, Xuan
Che, Nanying
Zhang, Tongmei
Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients
title Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients
title_full Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients
title_fullStr Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients
title_full_unstemmed Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients
title_short Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients
title_sort comprehensive comparative molecular characterization of young and old lung cancer patients
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789686/
https://www.ncbi.nlm.nih.gov/pubmed/35096611
http://dx.doi.org/10.3389/fonc.2021.806845
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