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Genomic landscape of ground glass opacities (GGOs) in East Asians

BACKGROUND: Understanding the genomic landscape of early-stage lung adenocarcinoma (LUAD) may provide new insights into the molecular evolution in the early stages of LUAD. METHODS: Through sequencing of 79 spatially distinct regions from 37 patients with ground glass opacities (GGOs), we provided a...

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Autores principales: Cao, Peng, Hu, Shan, Kong, Kangle, Han, Peng, Yue, Jiaqi, Deng, Yu, Zhao, Bo, Li, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107556/
https://www.ncbi.nlm.nih.gov/pubmed/34012587
http://dx.doi.org/10.21037/jtd-21-82
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author Cao, Peng
Hu, Shan
Kong, Kangle
Han, Peng
Yue, Jiaqi
Deng, Yu
Zhao, Bo
Li, Fan
author_facet Cao, Peng
Hu, Shan
Kong, Kangle
Han, Peng
Yue, Jiaqi
Deng, Yu
Zhao, Bo
Li, Fan
author_sort Cao, Peng
collection PubMed
description BACKGROUND: Understanding the genomic landscape of early-stage lung adenocarcinoma (LUAD) may provide new insights into the molecular evolution in the early stages of LUAD. METHODS: Through sequencing of 79 spatially distinct regions from 37 patients with ground glass opacities (GGOs), we provided a comprehensive mutational landscape of GGOs, highlighting the importance of ancestry differences. RESULTS: Our study had several interesting features. First, epidermal growth factor receptor (EGFR), BRAF (v-RAF murine sarcoma viral oncogene homologue B1), and ERBB2 (Erb-B2 Receptor Tyrosine Kinase 2, also known as HER2) were more frequently mutated in our study, which supports the notion that EGFR is considered to be a major driver and tends to drive the occurrence of LUAD. Second, Signature 1, Signature 3, and Signature 6 were identified in patients with GGOs. Our results further suggested that Signature 1 was more prominent among early mutations. Third, compared with LUADs, GGOs exhibited significantly lower levers of arm-level copy number variation (CNV)—which alter the diploid status of DNA, and lower focal CNVs. CONCLUSIONS: In our study, 79 samples of patients were included to analyze the GGO gene profile, revealing the genetic heterogeneity of GGO in East Asian population, and providing guidance for prognosis analysis of GGO patients by comparison with LUAD. Our study revealed that GGOs had fewer genomic alterations and simpler genomic profiles than LUADs. The most commonly altered processes were related to the receptor tyrosine kinase (RTK)/Ras/phosphatidylinositol-3-kinase (PI3K) signaling pathways in GGOs, and EGFR alterations were the dominant genetic changes across all targetable somatic changes.
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spelling pubmed-81075562021-05-18 Genomic landscape of ground glass opacities (GGOs) in East Asians Cao, Peng Hu, Shan Kong, Kangle Han, Peng Yue, Jiaqi Deng, Yu Zhao, Bo Li, Fan J Thorac Dis Original Article BACKGROUND: Understanding the genomic landscape of early-stage lung adenocarcinoma (LUAD) may provide new insights into the molecular evolution in the early stages of LUAD. METHODS: Through sequencing of 79 spatially distinct regions from 37 patients with ground glass opacities (GGOs), we provided a comprehensive mutational landscape of GGOs, highlighting the importance of ancestry differences. RESULTS: Our study had several interesting features. First, epidermal growth factor receptor (EGFR), BRAF (v-RAF murine sarcoma viral oncogene homologue B1), and ERBB2 (Erb-B2 Receptor Tyrosine Kinase 2, also known as HER2) were more frequently mutated in our study, which supports the notion that EGFR is considered to be a major driver and tends to drive the occurrence of LUAD. Second, Signature 1, Signature 3, and Signature 6 were identified in patients with GGOs. Our results further suggested that Signature 1 was more prominent among early mutations. Third, compared with LUADs, GGOs exhibited significantly lower levers of arm-level copy number variation (CNV)—which alter the diploid status of DNA, and lower focal CNVs. CONCLUSIONS: In our study, 79 samples of patients were included to analyze the GGO gene profile, revealing the genetic heterogeneity of GGO in East Asian population, and providing guidance for prognosis analysis of GGO patients by comparison with LUAD. Our study revealed that GGOs had fewer genomic alterations and simpler genomic profiles than LUADs. The most commonly altered processes were related to the receptor tyrosine kinase (RTK)/Ras/phosphatidylinositol-3-kinase (PI3K) signaling pathways in GGOs, and EGFR alterations were the dominant genetic changes across all targetable somatic changes. AME Publishing Company 2021-04 /pmc/articles/PMC8107556/ /pubmed/34012587 http://dx.doi.org/10.21037/jtd-21-82 Text en 2021 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Cao, Peng
Hu, Shan
Kong, Kangle
Han, Peng
Yue, Jiaqi
Deng, Yu
Zhao, Bo
Li, Fan
Genomic landscape of ground glass opacities (GGOs) in East Asians
title Genomic landscape of ground glass opacities (GGOs) in East Asians
title_full Genomic landscape of ground glass opacities (GGOs) in East Asians
title_fullStr Genomic landscape of ground glass opacities (GGOs) in East Asians
title_full_unstemmed Genomic landscape of ground glass opacities (GGOs) in East Asians
title_short Genomic landscape of ground glass opacities (GGOs) in East Asians
title_sort genomic landscape of ground glass opacities (ggos) in east asians
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107556/
https://www.ncbi.nlm.nih.gov/pubmed/34012587
http://dx.doi.org/10.21037/jtd-21-82
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