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Mediastinal germ cell tumors: many questions and perhaps an answer
by
Looijenga, Leendert H.J.
, Oosterhuis, J. Wolter
in
Care and treatment
/ Diagnosis
/ DNA Copy Number Variations
/ Gene mutation
/ Genetic aspects
/ Germinoma
/ Health aspects
/ Hematologic Neoplasms
/ Humans
/ Male
/ Neoplasms, Germ Cell and Embryonal - genetics
/ Phylogeny
/ Testicular Neoplasms
/ Tumor proteins
2020
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Mediastinal germ cell tumors: many questions and perhaps an answer
by
Looijenga, Leendert H.J.
, Oosterhuis, J. Wolter
in
Care and treatment
/ Diagnosis
/ DNA Copy Number Variations
/ Gene mutation
/ Genetic aspects
/ Germinoma
/ Health aspects
/ Hematologic Neoplasms
/ Humans
/ Male
/ Neoplasms, Germ Cell and Embryonal - genetics
/ Phylogeny
/ Testicular Neoplasms
/ Tumor proteins
2020
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Do you wish to request the book?
Mediastinal germ cell tumors: many questions and perhaps an answer
by
Looijenga, Leendert H.J.
, Oosterhuis, J. Wolter
in
Care and treatment
/ Diagnosis
/ DNA Copy Number Variations
/ Gene mutation
/ Genetic aspects
/ Germinoma
/ Health aspects
/ Hematologic Neoplasms
/ Humans
/ Male
/ Neoplasms, Germ Cell and Embryonal - genetics
/ Phylogeny
/ Testicular Neoplasms
/ Tumor proteins
2020
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Mediastinal germ cell tumors: many questions and perhaps an answer
Journal Article
Mediastinal germ cell tumors: many questions and perhaps an answer
2020
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Overview
Some germ cell tumors (GCTs) in men develop into hematologic malignancies; however, the clonal origins of such malignancies remain unknown. In this issue of the JCI, Taylor, Donoghue, et al. unravel the clonal relationship between primary mediastinal nonseminomas (PMNs) and hematologic somatic-type malignancies (HSTMs). Whole-exome sequencing was used to construct phylogenetic trees of the PMNs and the ensuing HSTM clones. HSTMs were derived from multiple distinct clones not detected within the PMNs. Clones from PMNs and HSTMs shared a common precursor, arguably an embryonal carcinoma cell resulting from a reprogrammed primordial germ cell from the thymus. Mutational and copy number variation analysis of a large cohort of patients with PMNs also demonstrated a high prevalence of TP53 mutations not found in testicular nonseminomas. These data likely explain why patients with PMNs are frequently resistant to platinum-based chemotherapy and provide TP53 mutations as potential targets.
Publisher
American Society for Clinical Investigation
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