Gene Expression Profiles of Multiple Synchronous Lesions in Lung Adenocarcinoma.
Jisun LimYeon Bi HanSoo Young ParkSoyeon AhnHyojin KimHyun Jung KwonChoon-Taek LeeSukki ChoJin-Haeng ChungPublished in: Cells (2021)
Many studies support a stepwise continuum of morphologic changes between atypical adenomatous hyperplasia (AAH) and lung adenocarcinoma (ADC). Here we characterized gene expression patterns and the association of differentially expressed genes and immune tumor microenvironment behaviors in AAH to ADC during ADC development. Tumor tissues from nine patients with ADC and synchronous multiple ground glass nodules/lesions (GGN/Ls) were analyzed using RNA sequencing. Using clustering, we identified genes differentially and sequentially expressed in AAH and ADC compared to normal tissues. Functional enrichment analysis using gene ontology terms was performed, and the fraction of immune cell types was estimated. We identified up-regulated genes ( ACSL5 and SERINC2 ) with a stepwise change of expression from AAH to ADC and validated those expressions by quantitative PCR and immunohistochemistry. The immune cell profiles revealed increased B cell activities and decreased natural killer cell activities in AAH and ADC. A stepwise change of differential expression during ADC development revealed potential effects on immune function in synchronous precursors and in tumor lesions in patients with lung cancer.
Keyphrases
- gene expression
- diffusion weighted imaging
- diffusion weighted
- single cell
- genome wide
- contrast enhanced
- dna methylation
- genome wide identification
- poor prognosis
- rna seq
- transcription factor
- computed tomography
- stem cells
- magnetic resonance
- copy number
- cell therapy
- genome wide analysis
- mass spectrometry
- mesenchymal stem cells