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Published on: September 20, 2016
Common Oncogene Mutations and Novel SND1-BRAF Transcript Fusion in Lung Adenocarcinoma from Never Smokers
Jin Sung Jang1, Adam Lee2, Jun Li1,3
1Departments of Medicine, Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN.
Abstract:
Lung adenocarcinomas from never smokers account for approximately 15 to 20% of all lung cancers and these tumors often carry genetic alterations that are responsive to targeted therapy. Here we examined mutation status in 10 oncogenes among 89 lung adenocarcinomas from never smokers. We also screened for oncogene fusion transcripts in 20 of the 89 tumors by RNA-Seq. In total, 62 tumors had mutations in at least one of the 10 oncogenes, including EGFR (49 cases, 55%), K-ras (5 cases, 6%), BRAF (4 cases, 5%), PIK3CA (3 cases, 3%), and ERBB2 (4 cases, 5%). In addition to ALK fusions identified by IHC/FISH in four cases, two previously known fusions involving EZR- ROS1 and KIF5B-RET were identified by RNA-Seq as well as a third novel fusion transcript that was formed between exons 1-9 of SND1 and exons 2 to 3' end of BRAF. This in-frame fusion was observed in 3/89 tested tumors and 2/64 additional never smoker lung adenocarcinoma samples. Ectopic expression of SND1-BRAF in H1299 cells increased phosphorylation levels of MEK/ERK, cell proliferation, and spheroid formation compared to parental mock-transfected control. Jointly, our results suggest a potential role of the novel BRAF fusion in lung cancer development and therapy.
Insights
Researchers identified a novel SND1-BRAF fusion in lung adenocarcinomas from never-smokers. This genetic alteration may play a role in cancer development and offers a potential target for future therapies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Lung adenocarcinomas in never-smokers represent a distinct subset of lung cancer, often driven by targetable genetic alterations.
- Understanding the molecular landscape of these tumors is crucial for developing effective targeted therapies.
Purpose of the Study:
- To investigate oncogene mutation status and identify fusion transcripts in lung adenocarcinomas from never-smokers.
- To characterize a novel BRAF fusion and assess its functional impact on cancer cells.
Main Methods:
- Genomic DNA sequencing of 10 oncogenes in 89 tumors.
- RNA sequencing (RNA-Seq) to screen for oncogene fusions in 20 tumors.
- Functional assays involving ectopic expression of the identified fusion transcript.
Main Results:
- Mutations were found in EGFR, K-ras, BRAF, PIK3CA, and ERBB2.
- ALK, EZR-ROS1, and KIF5B-RET fusions were identified.
- A novel in-frame SND1-BRAF fusion was discovered in multiple samples and shown to enhance cell proliferation and signaling pathways (MEK/ERK) upon ectopic expression.
Conclusions:
- The novel SND1-BRAF fusion is a potential driver in a subset of lung adenocarcinomas in never-smokers.
- This fusion represents a promising new therapeutic target for lung cancer treatment.
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