Lineage-Independent Tumors in Bilateral Neuroblastoma
Author(s) -
Tim H. H. Coorens,
Sarah J. Farndon,
Thomas J. Mitchell,
Neha Jain,
Sang-Jin Lee,
Michael Hubank,
Neil J. Sebire,
John Anderson,
Sam Behjati
Publication year - 2020
Publication title -
new england journal of medicine
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa2000962
Subject(s) - neuroblastoma , germline , smarca4 , biology , lineage (genetic) , germline mutation , somatic cell , genotyping , clone (java method) , cancer research , mutation , pathology , gene , genetics , medicine , genotype , transcription factor , cell culture , chromatin remodeling
Childhood tumors that occur synchronously in different anatomical sites usually represent metastatic disease. However, such tumors can be independent neoplasms. We investigated whether cases of bilateral neuroblastoma represented independent tumors in two children with pathogenic germline mutations by genotyping somatic mutations shared between tumors and blood. Our results suggested that in both children, the lineages that had given rise to the tumors had segregated within the first cell divisions of the zygote, without being preceded by a common premalignant clone. In one patient, the tumors had parallel evolution, including distinct second hits in SMARCA4 , a putative predisposition gene for neuroblastoma. These findings portray cases of bilateral neuroblastoma as having independent lesions mediated by a germline predisposition. (Funded by Children with Cancer UK and Wellcome.).
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