Somatic substitution signature as an innovative tool in lung cancer diagnosis

Abstract Diagnosis of lung cancer can sometimes be challenging and is of major interest since effective molecular-guided therapies are available. Compounds of tobacco smoke may generate a specific substitutional signature in lung, which is the most exposed organ. To predict whether a tumor is of lun...

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Main Authors: Stéphane Busca, Julia Salleron, Romain Boidot, Jean-Louis Merlin, Alexandre Harlé
Format: Article
Language:English
Published: Nature Publishing Group 2019-10-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-019-51155-3
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spelling doaj-b87948ed20474dea8a6fabbf8e342a862020-12-08T09:08:46ZengNature Publishing GroupScientific Reports2045-23222019-10-01911910.1038/s41598-019-51155-3Somatic substitution signature as an innovative tool in lung cancer diagnosisStéphane Busca0Julia Salleron1Romain Boidot2Jean-Louis Merlin3Alexandre Harlé4Service de Biopathologie, Institut de Cancérologie de LorraineData Biostatistics Unit, Institut de Cancérologie de LorraineDepartment of Tumor Biology and Pathology, Georges-Francois Leclerc Cancer Center – UNICANCERService de Biopathologie, Institut de Cancérologie de LorraineService de Biopathologie, Institut de Cancérologie de LorraineAbstract Diagnosis of lung cancer can sometimes be challenging and is of major interest since effective molecular-guided therapies are available. Compounds of tobacco smoke may generate a specific substitutional signature in lung, which is the most exposed organ. To predict whether a tumor is of lung origin or not, we developed and validated the EASILUNG (Exome And SIgnature LUNG) test based on the relative frequencies of somatic substitutions on coding non-transcribed DNA strands from whole-exome sequenced tumors. Data from 7,796 frozen tumor samples (prior to any treatment) from 32 TCGA solid cancer groups were used for its development. External validation was carried out on a local dataset of 196 consecutive routine exome results. Eight out of the 12 classes of substitutions were required to compute the EASILUNG signature that demonstrated good calibration and good discriminative power with a sensitivity of 83% and a specificity of 72% after recalibration on the external validation dataset. This innovative test may be helpful in medical decision-making in patients with unknown primary tumors potentially of lung origin and in the diagnosis of lung cancer in smokers.https://doi.org/10.1038/s41598-019-51155-3
collection DOAJ
language English
format Article
sources DOAJ
author Stéphane Busca
Julia Salleron
Romain Boidot
Jean-Louis Merlin
Alexandre Harlé
spellingShingle Stéphane Busca
Julia Salleron
Romain Boidot
Jean-Louis Merlin
Alexandre Harlé
Somatic substitution signature as an innovative tool in lung cancer diagnosis
Scientific Reports
author_facet Stéphane Busca
Julia Salleron
Romain Boidot
Jean-Louis Merlin
Alexandre Harlé
author_sort Stéphane Busca
title Somatic substitution signature as an innovative tool in lung cancer diagnosis
title_short Somatic substitution signature as an innovative tool in lung cancer diagnosis
title_full Somatic substitution signature as an innovative tool in lung cancer diagnosis
title_fullStr Somatic substitution signature as an innovative tool in lung cancer diagnosis
title_full_unstemmed Somatic substitution signature as an innovative tool in lung cancer diagnosis
title_sort somatic substitution signature as an innovative tool in lung cancer diagnosis
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2019-10-01
description Abstract Diagnosis of lung cancer can sometimes be challenging and is of major interest since effective molecular-guided therapies are available. Compounds of tobacco smoke may generate a specific substitutional signature in lung, which is the most exposed organ. To predict whether a tumor is of lung origin or not, we developed and validated the EASILUNG (Exome And SIgnature LUNG) test based on the relative frequencies of somatic substitutions on coding non-transcribed DNA strands from whole-exome sequenced tumors. Data from 7,796 frozen tumor samples (prior to any treatment) from 32 TCGA solid cancer groups were used for its development. External validation was carried out on a local dataset of 196 consecutive routine exome results. Eight out of the 12 classes of substitutions were required to compute the EASILUNG signature that demonstrated good calibration and good discriminative power with a sensitivity of 83% and a specificity of 72% after recalibration on the external validation dataset. This innovative test may be helpful in medical decision-making in patients with unknown primary tumors potentially of lung origin and in the diagnosis of lung cancer in smokers.
url https://doi.org/10.1038/s41598-019-51155-3
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