posted on 2008-12-01, 15:34authored byPaolo Salomoni, Brian J. Ferguson, A. H. Wyllie, Tina Rich
The PML gene is involved in the t(15;17) translocation of acute promyelocytic
leukaemia (APL), which generates the oncogenic fusion protein PML-RAR. The
PML protein localises to a subnuclear structure called the PML nuclear domain
(PML-ND), of which PML is the essential structural component. In APL, PML-NDs
are disrupted thus implicating these structures in the pathogenesis of this
leukaemia. Unexpectedly, recent studies indicate that PML and the PML-ND play a
tumour suppressive role in several different types of human neoplasms in addition
to APL. Because of PML’s extreme versatility and involvement in multiple cellular
pathways, understanding the mechanisms underlying its function, and therefore
role in tumour suppression, have been a challenging task. In this review, we attempt
to critically appraise the more recent advances in this field and propose new
avenues of investigation.