TY - JOUR
T1 - The biology of germ cell tumors in disorders of sex development
AU - Hersmus, Remko
AU - van Bever, Yolande
AU - Wolffenbuttel, Katja P
AU - Biermann, Katharina
AU - Cools, Martine
AU - Looijenga, Leendert H J
N1 - © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2017/2
Y1 - 2017/2
N2 - Development of a malignant germ cell tumor, i.e., germ cell cancer (GCC) in individuals with disorders of sex development (DSD) depends on a number of (epi-)genetic factors related to early gonadal- and germ cell development, possibly related to genetic susceptibility. Fetal development of germ cells is orchestrated by strict processes involving specification, migration and the development of a proper gonadal niche. In this review we will discuss the early (epi-)genetic events in normal and aberrant germ cell and gonadal development. Focus will be on the formation of the precursor lesions of GCC in individuals who have DSD. In our view, expression of the different embryonic markers in, and epigenetic profile of the precursor lesions reflects the developmental stage in which these cells are blocked in their maturation. Therefore, these are not a primary pathogenetic driving force. Progression later in life towards a full blown cancer likely depends on additional factors such as a changed endocrine environment in a susceptible individual. Genetic susceptibility is, as evidenced by the presence of specific risk genetic variants (SNPs) in patients with a testicular GCC, related to genes involved in early germ cell and gonadal development.
AB - Development of a malignant germ cell tumor, i.e., germ cell cancer (GCC) in individuals with disorders of sex development (DSD) depends on a number of (epi-)genetic factors related to early gonadal- and germ cell development, possibly related to genetic susceptibility. Fetal development of germ cells is orchestrated by strict processes involving specification, migration and the development of a proper gonadal niche. In this review we will discuss the early (epi-)genetic events in normal and aberrant germ cell and gonadal development. Focus will be on the formation of the precursor lesions of GCC in individuals who have DSD. In our view, expression of the different embryonic markers in, and epigenetic profile of the precursor lesions reflects the developmental stage in which these cells are blocked in their maturation. Therefore, these are not a primary pathogenetic driving force. Progression later in life towards a full blown cancer likely depends on additional factors such as a changed endocrine environment in a susceptible individual. Genetic susceptibility is, as evidenced by the presence of specific risk genetic variants (SNPs) in patients with a testicular GCC, related to genes involved in early germ cell and gonadal development.
KW - Biomarkers, Tumor/genetics
KW - Disorders of Sex Development/genetics
KW - Endocrine System/metabolism
KW - Female
KW - Genetic Predisposition to Disease
KW - Germ Cells/metabolism
KW - Gonads/growth & development
KW - Humans
KW - Male
KW - Neoplasms, Germ Cell and Embryonal/genetics
KW - Polymorphism, Single Nucleotide/genetics
KW - Risk Factors
UR - http://www.scopus.com/inward/record.url?scp=85006013015&partnerID=8YFLogxK
U2 - 10.1111/cge.12882
DO - 10.1111/cge.12882
M3 - Review article
C2 - 27716895
SN - 0009-9163
VL - 91
SP - 292
EP - 301
JO - Clinical genetics
JF - Clinical genetics
IS - 2
ER -