TY - JOUR
T1 - Molecular correlates of male germ cell tumors with overgrowth of components resembling somatic malignancies
AU - Wyvekens, Nicolas
AU - Sholl, Lynette M.
AU - Yang, Yiying
AU - Tran, Ivy
AU - Vasudevaraja, Varshini
AU - Dickson, Brendan C.
AU - Al-Obaidy, Khaleel I.
AU - Baniak, Nicholas
AU - Collins, Katrina
AU - Gordetsky, Jennifer B.
AU - Idrees, Muhammad T.
AU - Kao, Chia Sui
AU - Maclean, Fiona
AU - Matoso, Andres
AU - Ulbright, Thomas M.
AU - Wobker, Sara E.
AU - Fletcher, Christopher D. M.
AU - Hirsch, Michelle S.
AU - Hornick, Jason L.
AU - Snuderl, Matija
AU - Acosta, Andres M.
PY - 2022/12
Y1 - 2022/12
N2 - A small subset of male germ cell tumors (GCT) demonstrates overgrowth of histologic components that resemble somatic malignancies (e.g., sarcoma, carcinoma). The presence of so-called “somatic-type” malignancies (SM) in GCT has been associated with chemotherapy-resistance and poor clinical outcomes in prior studies. However, the molecular characteristics of these tumors remain largely undescribed. In this study, we performed a multi-platform molecular analysis of GCTs with SM diagnosed in 36 male patients (primary site: testis, 29 and mediastinum, 7). The most common histologic types of SM were sarcoma and embryonic-type neuroectodermal tumor (ENT, formerly known as “PNET”), present in 61% and 31% of cases, respectively. KRAS and TP53 mutations were identified by DNA sequencing in 28% of cases each, with enrichment of TP53 mutations in mediastinal tumors (86%). Gains in the short arm of chromosome 12 were seen in 91% of cases, likely reflecting the presence of isochromosome 12p. Numerous copy number changes indicative of widespread aneuploidy were found in 94% of cases. Focal homozygous deletions and amplifications were also detected, including MDM2 amplifications in 16% of cases. Sequencing of paired samples in 8 patients revealed similar mutational and copy number profiles in the conventional GCT and SM components. Oncogenic gene fusions were not detected using RNA sequencing of SM components from 9 cases. DNA methylation analysis highlighted the distinct methylation profile of SM components that sets them apart from conventional GCT components. In conclusion, GCT with SM are characterized by widespread aneuploidy, a distinct epigenetic signature and the presence of mutations that are otherwise rare in testicular GCT without SM. The similarity of the mutational and DNA methylation profiles of different histologic types of SM suggests that the identification of SM components could be more important than their precise histologic subclassification, pending confirmation by further studies.
AB - A small subset of male germ cell tumors (GCT) demonstrates overgrowth of histologic components that resemble somatic malignancies (e.g., sarcoma, carcinoma). The presence of so-called “somatic-type” malignancies (SM) in GCT has been associated with chemotherapy-resistance and poor clinical outcomes in prior studies. However, the molecular characteristics of these tumors remain largely undescribed. In this study, we performed a multi-platform molecular analysis of GCTs with SM diagnosed in 36 male patients (primary site: testis, 29 and mediastinum, 7). The most common histologic types of SM were sarcoma and embryonic-type neuroectodermal tumor (ENT, formerly known as “PNET”), present in 61% and 31% of cases, respectively. KRAS and TP53 mutations were identified by DNA sequencing in 28% of cases each, with enrichment of TP53 mutations in mediastinal tumors (86%). Gains in the short arm of chromosome 12 were seen in 91% of cases, likely reflecting the presence of isochromosome 12p. Numerous copy number changes indicative of widespread aneuploidy were found in 94% of cases. Focal homozygous deletions and amplifications were also detected, including MDM2 amplifications in 16% of cases. Sequencing of paired samples in 8 patients revealed similar mutational and copy number profiles in the conventional GCT and SM components. Oncogenic gene fusions were not detected using RNA sequencing of SM components from 9 cases. DNA methylation analysis highlighted the distinct methylation profile of SM components that sets them apart from conventional GCT components. In conclusion, GCT with SM are characterized by widespread aneuploidy, a distinct epigenetic signature and the presence of mutations that are otherwise rare in testicular GCT without SM. The similarity of the mutational and DNA methylation profiles of different histologic types of SM suggests that the identification of SM components could be more important than their precise histologic subclassification, pending confirmation by further studies.
UR - http://www.scopus.com/inward/record.url?scp=85137024028&partnerID=8YFLogxK
U2 - 10.1038/s41379-022-01136-1
DO - 10.1038/s41379-022-01136-1
M3 - Article
C2 - 36030288
AN - SCOPUS:85137024028
SN - 0893-3952
VL - 35
SP - 1966
EP - 1973
JO - Modern Pathology
JF - Modern Pathology
IS - 12
ER -