TY - JOUR
T1 - How germline genes promote malignancy in cancer cells
AU - Bruggeman, Jan Willem
AU - Koster, Jan
AU - van Pelt, Ans M. M.
AU - Speijer, Dave
AU - Hamer, Geert
N1 - Funding Information: The authors thank the De Snoo van't Hoogerhuijs foundation and the Amsterdam Reproduction and Development Research Institute for their financial support of this project. Publisher Copyright: © 2022 The Authors. BioEssays published by Wiley Periodicals LLC.
PY - 2023/1
Y1 - 2023/1
N2 - Cancers often express hundreds of genes otherwise specific to germ cells, the germline/cancer (GC) genes. Here, we present and discuss the hypothesis that activation of a “germline program” promotes cancer cell malignancy. We do so by proposing four hallmark processes of the germline: meiosis, epigenetic plasticity, migration, and metabolic plasticity. Together, these hallmarks enable replicative immortality of germ cells as well as cancer cells. Especially meiotic genes are frequently expressed in cancer, implying that genes unique to meiosis may play a role in oncogenesis. Because GC genes are not expressed in healthy somatic tissues, they form an appealing source of specific treatment targets with limited side effects besides infertility. Although it is still unclear why germ cell specific genes are so abundantly expressed in cancer, from our hypothesis it follows that the germline's reproductive program is intrinsic to cancer development.
AB - Cancers often express hundreds of genes otherwise specific to germ cells, the germline/cancer (GC) genes. Here, we present and discuss the hypothesis that activation of a “germline program” promotes cancer cell malignancy. We do so by proposing four hallmark processes of the germline: meiosis, epigenetic plasticity, migration, and metabolic plasticity. Together, these hallmarks enable replicative immortality of germ cells as well as cancer cells. Especially meiotic genes are frequently expressed in cancer, implying that genes unique to meiosis may play a role in oncogenesis. Because GC genes are not expressed in healthy somatic tissues, they form an appealing source of specific treatment targets with limited side effects besides infertility. Although it is still unclear why germ cell specific genes are so abundantly expressed in cancer, from our hypothesis it follows that the germline's reproductive program is intrinsic to cancer development.
KW - Cancer
KW - cancer/testis genes (CT genes)
KW - germline
KW - germline/cancer genes (GC genes)
KW - oncogenesis
KW - reproduction
UR - http://www.scopus.com/inward/record.url?scp=85141349910&partnerID=8YFLogxK
U2 - https://doi.org/10.1002/bies.202200112
DO - https://doi.org/10.1002/bies.202200112
M3 - Article
C2 - 36300921
VL - 45
JO - BioEssays
JF - BioEssays
SN - 0265-9247
IS - 1
M1 - 2200112
ER -