Co-occurring Genomic Alterations Define Major Subsets of KRAS -Mutant Lung Adenocarcinoma with Distinct Biology, Immune Profiles, and Therapeutic Vulnerabilities
The University of Texas MD Anderson Cancer Center · The University of Texas Southwestern Medical Center · +5 more institutions
Abstract
UNLABELLED: The molecular underpinnings that drive the heterogeneity of KRAS-mutant lung adenocarcinoma are poorly characterized. We performed an integrative analysis of genomic, transcriptomic, and proteomic data from early-stage and chemorefractory lung adenocarcinoma and identified three robust subsets of KRAS-mutant lung adenocarcinoma dominated, respectively, by co-occurring genetic events in STK11/LKB1 (the KL subgroup), TP53 (KP), and CDKN2A/B inactivation coupled with low expression of the NKX2-1 (TTF1) transcription factor (KC). We further revealed biologically and therapeutically relevant differences between the subgroups. KC tumors frequently exhibited mucinous histology and suppressed mTORC1…
Citation impact
- FWCI
- 44.80
- Percentile
- 100%
- References
- 60
Authors
37- FSFerdinandos SkoulidisCorresponding
The University of Texas MD Anderson Cancer Center
- LALauren A. Byers
The University of Texas MD Anderson Cancer Center
- LDLixia Diao
The University of Texas MD Anderson Cancer Center
- VAVassiliki A. Papadimitrakopoulou
The University of Texas MD Anderson Cancer Center
- PTPan Tong
The University of Texas MD Anderson Cancer Center
Topics & keywords
- KRAS
- Biology
- STK11
- Adenocarcinoma
- CDKN2A
- Cancer research
- Transcriptome
- Immune system
- Good health and well-being