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Genomic alterations of ground-glass nodular lung adenocarcinoma.
- Source :
-
Scientific reports [Sci Rep] 2018 May 16; Vol. 8 (1), pp. 7691. Date of Electronic Publication: 2018 May 16. - Publication Year :
- 2018
-
Abstract
- 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.
- Subjects :
- Adenocarcinoma of Lung pathology
Adenocarcinoma of Lung virology
Aged
Case-Control Studies
Female
Gene Expression Profiling
Genome, Viral
High-Throughput Nucleotide Sequencing
Humans
Lung Neoplasms pathology
Lung Neoplasms virology
Male
Middle Aged
Adenocarcinoma of Lung genetics
Biomarkers, Tumor genetics
Genomics methods
Lung Neoplasms genetics
Oncogene Proteins, Fusion
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 8
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 29769567
- Full Text :
- https://doi.org/10.1038/s41598-018-25800-2