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Large-scale Analysis of Acquired Chromosomal Alterations in Non-tumor Samples from Patients with Cancer

Overview
Journal Nat Biotechnol
Specialty Biotechnology
Date 2019 Nov 6
PMID 31685958
Citations 28
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Abstract

Mosaicism, the presence of subpopulations of cells bearing somatic mutations, is associated with disease and aging and has been detected in diverse tissues, including apparently normal cells adjacent to tumors. To analyze mosaicism on a large scale, we surveyed haplotype-specific somatic copy number alterations (sCNAs) in 1,708 normal-appearing adjacent-to-tumor (NAT) tissue samples from 27 cancer sites and in 7,149 blood samples from The Cancer Genome Atlas. We find substantial variation across tissues in the rate, burden and types of sCNAs, including those spanning entire chromosome arms. We document matching sCNAs in the NAT tissue and the adjacent tumor, suggesting a shared clonal origin, as well as instances in which both NAT tissue and tumor tissue harbor a gain of the same oncogene arising in parallel from distinct parental haplotypes. These results shed light on pan-tissue mutations characteristic of field cancerization, the presence of oncogenic processes adjacent to cancer cells.

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References
1.
Laurie C, Laurie C, Rice K, Doheny K, Zelnick L, McHugh C . Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet. 2012; 44(6):642-50. PMC: 3366033. DOI: 10.1038/ng.2271. View

2.
Freed D, Stevens E, Pevsner J . Somatic mosaicism in the human genome. Genes (Basel). 2014; 5(4):1064-94. PMC: 4276927. DOI: 10.3390/genes5041064. View

3.
Fowler J, San Lucas F, Scheet P . System for Quality-Assured Data Analysis: Flexible, reproducible scientific workflows. Genet Epidemiol. 2018; 43(2):227-237. PMC: 6571143. DOI: 10.1002/gepi.22178. View

4.
Martincorena I, Roshan A, Gerstung M, Ellis P, Van Loo P, McLaren S . Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin. Science. 2015; 348(6237):880-6. PMC: 4471149. DOI: 10.1126/science.aaa6806. View

5.
Kadara H, Sivakumar S, Jakubek Y, San Lucas F, Lang W, McDowell T . Driver Mutations in Normal Airway Epithelium Elucidate Spatiotemporal Resolution of Lung Cancer. Am J Respir Crit Care Med. 2019; 200(6):742-750. PMC: 6775870. DOI: 10.1164/rccm.201806-1178OC. View