Genomic imprinting refers to the parental origin-specific functional d
ifference between the paternally and maternally-derived mammalian hapl
oid genome. Normal embryogenesis depends on the presence of both a pat
ernal and a maternal copy of particular chromosomal regions, containin
g the so-called imprinted genes. Genomic imprinting is established som
ewhere in the maturation from a primordial germ cell to a mature gamet
e, either spermatid or oocyte. We discuss the value of testicular canc
ers, especially those derived from the germ cell lineage, as a model t
o study erasement of the biparental pattern of genomic imprinting as p
resent in the zygote and establishment of the paternal pattern during
spermatogenesis. In addition, we will present data on the presence of
X-inactivation in these cancers.