Expression of prothymosin alpha (PTA) has been related to cell proliferatio
n, both normal and pathological. PTA has also been proposed to be a target
of the c-myc protooncogene. To study PTA mRNA levels during pathological ce
ll growth, and especially the effect of the activation of specific oncogene
s on PTA expression, we have studied its expression in tumors that arise in
transgenic mice. We found high PTA levels in mammary tumors arising in c-m
yc, c-neu, and v-ras transgenic mice. Levels of this protein were variable
between different tumors, and there is a differential regulation of PTA res
pect to other putative c-myc target genes, such as Ornithine Decarboxylase
(ODC). Furthermore, expression of PTA is not absolutely dependent of c-myc
expression, as shown by MYC depletion experiments performed with antisense
oligonucleotides. We conclude that regulation of PTA in these tumors is com
plex and depends on more than a single activated oncogene.