Mosaic chromosomal alterations are associated with increased lung cancer risk: insight from the INTEGRAL-ILCCO cohort analysis

Introduction - Mosaic chromosomal alterations (mCAs) detected in white blood cells represent a type of clonal hematopoiesis (CH) that is understudied compared with CH-related somatic mutations. A few recent studies indicated their potential link with nonhematological cancers, especially lung cancer....

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Hauptverfasser: Cheng, Chao (VerfasserIn) , Hong, Wei (VerfasserIn) , Li, Yafang (VerfasserIn) , Xiao, Xiangjun (VerfasserIn) , McKay, James (VerfasserIn) , Han, Younghun (VerfasserIn) , Byun, Jinyoung (VerfasserIn) , Peng, Bo (VerfasserIn) , Albanes, Demetrios (VerfasserIn) , Lam, Stephen (VerfasserIn) , Tardon, Adonina (VerfasserIn) , Chen, Chu (VerfasserIn) , Bojesen, Stig E. (VerfasserIn) , Landi, Maria T. (VerfasserIn) , Johansson, Mattias (VerfasserIn) , Risch, Angela (VerfasserIn) , Bickeböller, Heike (VerfasserIn) , Wichmann, H-Erich (VerfasserIn) , Christiani, David C. (VerfasserIn) , Rennert, Gad (VerfasserIn) , Arnold, Susanne (VerfasserIn) , Goodman, Gary (VerfasserIn) , Field, John K. (VerfasserIn) , Davies, Michael P. A. (VerfasserIn) , Shete, Sanjay S. (VerfasserIn) , Le Marchand, Loic (VerfasserIn) , Liu, Geoffrey (VerfasserIn) , Hung, Rayjean J. (VerfasserIn) , Andrew, Angeline S. (VerfasserIn) , Kiemeney, Lambertus A. (VerfasserIn) , Zhu, Meng (VerfasserIn) , Shen, Hongbing (VerfasserIn) , Zienolddiny, Shan (VerfasserIn) , Grankvist, Kjell (VerfasserIn) , Johansson, Mikael (VerfasserIn) , Cox, Angela (VerfasserIn) , Hong, Yun-Chul (VerfasserIn) , Yuan, Jian-Min (VerfasserIn) , Lazarus, Philip (VerfasserIn) , Schabath, Matthew B. (VerfasserIn) , Aldrich, Melinda C. (VerfasserIn) , Brennan, Paul (VerfasserIn) , Li, Yong (VerfasserIn) , Gorlova, Olga (VerfasserIn) , Gorlov, Ivan (VerfasserIn) , Amos, Christopher I. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August 2023
In: Journal of thoracic oncology
Year: 2023, Jahrgang: 18, Heft: 8, Pages: 1003-1016
ISSN:1556-1380
DOI:10.1016/j.jtho.2023.05.001
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.jtho.2023.05.001
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S1556086423005270
Volltext
Verfasserangaben:Chao Cheng, Wei Hong, Yafang Li, Xiangjun Xiao, James McKay, Younghun Han, Jinyoung Byun, Bo Peng, Demetrios Albanes, Stephen Lam, Adonina Tardon, Chu Chen, Stig E. Bojesen, Maria T. Landi, Mattias Johansson, Angela Risch, Heike Bickeböller, H-Erich Wichmann, David C. Christiani, Gad Rennert, Susanne Arnold, Gary Goodman, John K. Field, Michael P. A. Davies, Sanjay S. Shete, Loic Le Marchand, Geoffrey Liu, Rayjean J. Hung, Angeline S. Andrew, Lambertus A. Kiemeney, Meng Zhu, Hongbing Shen, Shan Zienolddiny, Kjell Grankvist, Mikael Johansson, Angela Cox, Yun-Chul Hong, Jian-Min Yuan, Philip Lazarus, Matthew B. Schabath, Melinda C. Aldrich, Paul Brennan, Yong Li, Olga Gorlova, Ivan Gorlov, Christopher I. Amos

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520 |a Introduction - Mosaic chromosomal alterations (mCAs) detected in white blood cells represent a type of clonal hematopoiesis (CH) that is understudied compared with CH-related somatic mutations. A few recent studies indicated their potential link with nonhematological cancers, especially lung cancer. - Methods - In this study, we investigated the association between mCAs and lung cancer using the high-density genotyping data from the OncoArray study of INTEGRAL-ILCCO, the largest single genetic study of lung cancer with 18,221 lung cancer cases and 14,825 cancer-free controls. - Results - We identified a comprehensive list of autosomal mCAs, ChrX mCAs, and mosaic ChrY (mChrY) losses from these samples. Autosomal mCAs were detected in 4.3% of subjects, in addition to ChrX mCAs in 3.6% of females and mChrY losses in 9.6% of males. Multivariable logistic regression analysis indicated that the presence of autosomal mCAs in white blood cells was associated with an increased lung cancer risk after adjusting for key confounding factors, including age, sex, smoking status, and race. This association was mainly driven by a specific type of mCAs: copy-neutral loss of heterozygosity on autosomal chromosomes. The association between autosome copy-neutral loss of heterozygosity and increased risk of lung cancer was further confirmed in two major histologic subtypes, lung adenocarcinoma and squamous cell carcinoma. In addition, we observed a significant increase of ChrX mCAs and mChrY losses in smokers compared with nonsmokers and racial differences in certain types of mCA events. - Conclusions - Our study established a link between mCAs in white blood cells and increased risk of lung cancer. 
650 4 |a Clonal hematopoiesis 
650 4 |a Loss of heterozygosity 
650 4 |a Lung cancer risk 
650 4 |a Mosaic chromosomal alterations 
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