TY - JOUR
T1 - Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplant
AU - Gingras, Marie Claude
AU - Sabo, Aniko
AU - Cardenas, Maria
AU - Rana, Abbas
AU - Dhingra, Sadhna
AU - Meng, Qingchang
AU - Hu, Jianhong
AU - Muzny, Donna M.
AU - Doddapaneni, Harshavardhan
AU - Perez, Lesette
AU - Korchina, Viktoriya
AU - Nessner, Caitlin
AU - Liu, Xiuping
AU - Chao, Hsu
AU - Goss, John
AU - Gibbs, Richard A.
N1 - Publisher Copyright:
© 2021 Gingras et al.
PY - 2021/9
Y1 - 2021/9
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85112231391
UR - https://www.scopus.com/inward/citedby.url?scp=85112231391&partnerID=8YFLogxK
U2 - 10.26508/LSA.202000941
DO - 10.26508/LSA.202000941
M3 - Article
C2 - 34301805
AN - SCOPUS:85112231391
SN - 2575-1077
VL - 4
JO - Life Science Alliance
JF - Life Science Alliance
IS - 9
M1 - e202000941
ER -