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Genomic alterations of ground-glass nodular lung adenocarcinoma

In-depth molecular pathogenesis of ground-glass nodular lung adenocarcinoma has not been well understood. The objectives of this study were to identify genomic alterations in ground-glass nodular lung adenocarcinomas and to investigate whether viral transcripts were detected in these tumors. Nine pa...

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Autores principales: Lee, Hyun, Joung, Je-Gun, Shin, Hyun-Tae, Kim, Duk-Hwan, Kim, Yujin, Kim, Hojoong, Kwon, O. Jung, Shim, Young Mog, Lee, Ho Yun, Lee, Kyung Soo, Choi, Yoon-La, Park, Woong-Yang, Hayes, D. Neil, Um, Sang-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955945/
https://www.ncbi.nlm.nih.gov/pubmed/29769567
http://dx.doi.org/10.1038/s41598-018-25800-2
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author Lee, Hyun
Joung, Je-Gun
Shin, Hyun-Tae
Kim, Duk-Hwan
Kim, Yujin
Kim, Hojoong
Kwon, O. Jung
Shim, Young Mog
Lee, Ho Yun
Lee, Kyung Soo
Choi, Yoon-La
Park, Woong-Yang
Hayes, D. Neil
Um, Sang-Won
author_facet Lee, Hyun
Joung, Je-Gun
Shin, Hyun-Tae
Kim, Duk-Hwan
Kim, Yujin
Kim, Hojoong
Kwon, O. Jung
Shim, Young Mog
Lee, Ho Yun
Lee, Kyung Soo
Choi, Yoon-La
Park, Woong-Yang
Hayes, D. Neil
Um, Sang-Won
author_sort Lee, Hyun
collection PubMed
description In-depth molecular pathogenesis of ground-glass nodular lung adenocarcinoma has not been well understood. The objectives of this study were to identify genomic alterations in ground-glass nodular lung adenocarcinomas and to investigate whether viral transcripts were detected in these tumors. Nine patients with pure (n = 4) and part-solid (n = 5) ground-glass nodular adenocarcinomas were included. Six were females with a median age of 58 years. We performed targeted exon sequencing and RNA sequencing. EGFR (n = 10), IDH2 (n = 2), TP53 (n = 1), PTEN (n = 1), EPHB4 (n = 1), and BRAF (n = 1) were identified as driver mutations by targeted exon sequencing. Vasculogenesis-associated genes including NOTCH4 and TGFBR3 expression were significantly downregulated in adenocarcinoma tissue versus normal tissue (adjusted P values < 0.001 for both NOTCH4 and TGFBR3). In addition, five novel fusion gene loci were identified in four lung adenocarcinomas. However, no significant virus-associated transcripts were detected in tumors. In conclusions, EGFR, IDH2, TP53, PTEN, EPHB4, and BRAF were identified as putative driver mutations of ground-glass nodular adenocarcinomas. Five novel fusion genes were also identified in four tumors. Viruses do not appear to be involved in the tumorigenesis of ground-glass nodular lung adenocarcinoma.
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spelling pubmed-59559452018-05-21 Genomic alterations of ground-glass nodular lung adenocarcinoma Lee, Hyun Joung, Je-Gun Shin, Hyun-Tae Kim, Duk-Hwan Kim, Yujin Kim, Hojoong Kwon, O. Jung Shim, Young Mog Lee, Ho Yun Lee, Kyung Soo Choi, Yoon-La Park, Woong-Yang Hayes, D. Neil Um, Sang-Won Sci Rep Article In-depth molecular pathogenesis of ground-glass nodular lung adenocarcinoma has not been well understood. The objectives of this study were to identify genomic alterations in ground-glass nodular lung adenocarcinomas and to investigate whether viral transcripts were detected in these tumors. Nine patients with pure (n = 4) and part-solid (n = 5) ground-glass nodular adenocarcinomas were included. Six were females with a median age of 58 years. We performed targeted exon sequencing and RNA sequencing. EGFR (n = 10), IDH2 (n = 2), TP53 (n = 1), PTEN (n = 1), EPHB4 (n = 1), and BRAF (n = 1) were identified as driver mutations by targeted exon sequencing. Vasculogenesis-associated genes including NOTCH4 and TGFBR3 expression were significantly downregulated in adenocarcinoma tissue versus normal tissue (adjusted P values < 0.001 for both NOTCH4 and TGFBR3). In addition, five novel fusion gene loci were identified in four lung adenocarcinomas. However, no significant virus-associated transcripts were detected in tumors. In conclusions, EGFR, IDH2, TP53, PTEN, EPHB4, and BRAF were identified as putative driver mutations of ground-glass nodular adenocarcinomas. Five novel fusion genes were also identified in four tumors. Viruses do not appear to be involved in the tumorigenesis of ground-glass nodular lung adenocarcinoma. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955945/ /pubmed/29769567 http://dx.doi.org/10.1038/s41598-018-25800-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Hyun
Joung, Je-Gun
Shin, Hyun-Tae
Kim, Duk-Hwan
Kim, Yujin
Kim, Hojoong
Kwon, O. Jung
Shim, Young Mog
Lee, Ho Yun
Lee, Kyung Soo
Choi, Yoon-La
Park, Woong-Yang
Hayes, D. Neil
Um, Sang-Won
Genomic alterations of ground-glass nodular lung adenocarcinoma
title Genomic alterations of ground-glass nodular lung adenocarcinoma
title_full Genomic alterations of ground-glass nodular lung adenocarcinoma
title_fullStr Genomic alterations of ground-glass nodular lung adenocarcinoma
title_full_unstemmed Genomic alterations of ground-glass nodular lung adenocarcinoma
title_short Genomic alterations of ground-glass nodular lung adenocarcinoma
title_sort genomic alterations of ground-glass nodular lung adenocarcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955945/
https://www.ncbi.nlm.nih.gov/pubmed/29769567
http://dx.doi.org/10.1038/s41598-018-25800-2
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