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Life Sci Alliance ; 4(9)2021 09.
Article in English | MEDLINE | ID: mdl-34301805

ABSTRACT

Four organ transplant recipients from an organ donor diagnosed with anaplastic pleomorphic xanthoastrocytoma developed fatal malignancies for which the origin could not be confirmed by standard methods. We identified the somatic mutational profiles of the neoplasms using next-generation sequencing technologies and tracked the relationship between the different samples. The data were consistent with the presence of an aggressive clonal entity in the donor and the subsequent proliferation of descendent tumors in each recipient. Deleterious mutations in BRAF, PIK3CA, SDHC, DDR2, and FANCD2, and a chromosomal deletion spanning the CDKN2A/B genes, were shared between the recipients' lesions. In addition to demonstrating that DNA sequencing tracked a donor/recipient cancer transmission, this study established that the genetic profile of a donor tumor and its potential aggressive phenotype could have been determined before transplantation was considered. As the genetic correlates of tumor invasion and metastases become better known, adding genetic profiling by DNA sequencing to the data considered for transplant safety should be considered.


Subject(s)
Biomarkers, Tumor/genetics , Central Nervous System Neoplasms/etiology , Central Nervous System Neoplasms/pathology , Organ Transplantation/adverse effects , Sequence Analysis, DNA , Transplants/pathology , Adolescent , Adult , Biopsy , Central Nervous System Neoplasms/mortality , DNA Mutational Analysis , Female , Humans , INDEL Mutation , Male , Middle Aged , Mutation , Organ Transplantation/methods , Prognosis , Sequence Analysis, DNA/methods , Tissue Donors , Transplant Recipients , Exome Sequencing , Young Adult
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