| Literature DB >> 29410488 |
Won-Chul Lee1,2, Lixia Diao3, Jing Wang3, Jianhua Zhang1, Emily B Roarty2, Susan Varghese2, Chi-Wan Chow4, Junya Fujimoto4, Carmen Behrens2, Tina Cascone2, Weiyi Peng5, Neda Kalhor6, Cesar A Moran6, Annikka Weissferdt6, Faye M Johnson2, William N William2, Stephen G Swisher7, J Jack Lee8, Waun Ki Hong2, John V Heymach2, Ignacio I Wistuba9,10, P Andrew Futreal11, Jianjun Zhang12,13.
Abstract
Intra-tumor heterogeneity may be present at all molecular levels. Genomic intra-tumor heterogeneity at the exome level has been reported in many cancer types, but comprehensive gene expression intra-tumor heterogeneity has not been well studied. Here, we delineated the gene expression intra-tumor heterogeneity by exploring gene expression profiles of 35 tumor regions from 10 non-small cell lung cancer tumors (three or four regions/tumor), including adenocarcinoma, squamous cell carcinoma, large-cell carcinoma, and pleomorphic carcinoma of the lung. Using Affymetrix Gene 1.0 ST arrays, we generated the gene expression data for every sample. Inter-tumor heterogeneity was generally higher than intra-tumor heterogeneity, but some tumors showed a substantial level of intra-tumor heterogeneity. The analysis of various clinically relevant gene expression signatures including molecular subtype, epithelial-to-mesenchymal transition, and anti-PD-1 resistance signatures also revealed heterogeneity between different regions of the same tumor. The gene expression intra-tumor heterogeneity we observed was associated with heterogeneous tumor microenvironments represented by stromal and immune cells infiltrated. Our data suggest that RNA-based prognostic or predictive molecular tests should be carefully conducted in consideration of the gene expression intra-tumor heterogeneity.Entities:
Mesh:
Year: 2018 PMID: 29410488 DOI: 10.1038/s41379-018-0029-3
Source DB: PubMed Journal: Mod Pathol ISSN: 0893-3952 Impact factor: 7.842