Prognostic Significance of the Loss of Heterozygosity of KRAS in Early-Stage Lung Adenocarcinoma

被引:3
|
作者
Khadse, Anand [1 ,2 ]
Haakensen, Vilde D. [1 ,3 ]
Silwal-Pandit, Laxmi [1 ]
Hamfjord, Julian [1 ,3 ]
Micke, Patrick [4 ]
Botling, Johan [4 ]
Brustugun, Odd Terje [1 ,5 ]
Lingjaerde, Ole Christian [1 ,6 ]
Helland, Aslaug [1 ,3 ,7 ]
Kure, Elin H. [1 ,2 ]
机构
[1] Oslo Univ Hosp, Inst Canc Res, Dept Canc Genet, Oslo, Norway
[2] Univ South Eastern Norway, Fac ofTechnol, Dept Nat Sci & Environm Hlth, Nat Sci & Maritime Sci, Bo, Telemark, Norway
[3] Oslo Univ Hosp, Dept Oncol, Oslo, Norway
[4] Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab, Uppsala, Sweden
[5] Vestre Viken Hosp Trust, Drammen Hosp, Sect Oncol, Drammen, Norway
[6] Univ Oslo, Ctr Bioinformat, Dept Informat, Oslo, Norway
[7] Univ Oslo, Dept Clin Med, Oslo, Norway
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
关键词
KRAS; LOH; prognostic marker; copy number aberration; NSCLC; COPY NUMBER ALTERATIONS; MUTATION STATUS; NEVER SMOKERS; CANCER; TP53; GENOME; EXPRESSION; LANDSCAPE; SURVIVAL; EGFR;
D O I
10.3389/fonc.2022.873532
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is a common disease with a poor prognosis. Genomic alterations involving the KRAS gene are common in lung carcinomas, although much is unknown about how different mutations, deletions, and expressions influence the disease course. The first approval of a KRAS-directed inhibitor was recently approved by the FDA. Mutations in the KRAS gene have been associated with poor prognosis for lung adenocarcinomas, but implications of the loss of heterozygosity (LOH) of KRAS have not been investigated. In this study, we have assessed the LOH of KRAS in early-stage lung adenocarcinoma by analyzing DNA copy number profiles and have investigated the effect on patient outcome in association with mRNA expression and somatic hotspot mutations. KRAS mutation was present in 36% of cases and was associated with elevated mRNA expression. LOH in KRAS was associated with a favorable prognosis, more prominently in KRAS mutated than in wild-type patients. The presence of both LOH and mutation in KRAS conferred a better prognosis than KRAS mutation alone. For wild-type tumors, no difference in prognosis was observed between patients with and without LOH in KRAS. Our study indicates that LOH in KRAS is an independent prognostic factor that may refine the existing prognostic groups of lung adenocarcinomas.
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页数:11
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