TP53 mutation prevalence in normal airway epithelium as a biomarker for lung cancer risk

被引:2
作者
Craig, Daniel J. [1 ]
Crawford, Erin L. [1 ]
Chen, Heidi [2 ]
Grogan, Eric L. [2 ,3 ]
Deppen, Steven A. [2 ]
Morrison, Thomas [4 ]
Antic, Sanja L. [2 ]
Massion, Pierre P. [2 ]
Willey, James C. [1 ]
机构
[1] Univ Toledo, Coll Med, 3000 Arlington Ave, Toledo, OH 43614 USA
[2] Vanderbilt Univ, Med Ctr, 1301 Med Ctr Dr, Nashville, TN 37232 USA
[3] Tennessee Valley VA Healthcare Syst, 1310 24th Ave South, Nashville, TN 37212 USA
[4] Accugenomics Inc, 1410 Commonwealth Dr 105, Wilmington, NC 28403 USA
关键词
Lung cancer prevention; Lung cancer early detection; Biomarker; Next generation sequencing; TP53; Lung nodule risk classification; GENES; CELLS; STATISTICS; SIGNATURES;
D O I
10.1186/s12885-023-11266-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background There is a need for biomarkers that improve accuracy compared with current demographic risk indices to detect individuals at the highest lung cancer risk. Improved risk determination will enable more effective lung cancer screening and better stratification of lung nodules into high or low-risk category. We previously reported discovery of a biomarker for lung cancer risk characterized by increased prevalence of TP53 somatic mutations in airway epithelial cells (AEC). Here we present results from a validation study in an independent retrospective case-control cohort. Methods Targeted next generation sequencing was used to identify mutations within three TP53 exons spanning 193 base pairs in AEC genomic DNA. Results TP53 mutation prevalence was associated with cancer status (P < 0.001). The lung cancer detection receiver operator characteristic (ROC) area under the curve (AUC) for the TP53 biomarker was 0.845 (95% confidence limits 0.749-0.942). In contrast, TP53 mutation prevalence was not significantly associated with age or smoking pack-years. The combination of TP53 mutation prevalence with PLCOM2012 risk score had an ROC AUC of 0.916 (0.846-0.986) and this was significantly higher than that for either factor alone (P < 0.03). Conclusions These results support the validity of the TP53 mutation prevalence biomarker and justify taking additional steps to assess this biomarker in AEC specimens from a prospective cohort and in matched nasal brushing specimens as a potential non-invasive surrogate specimen.
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