We recently discovered that stathmin was overexpressed in a subgroup of hum
an breast carcinomas. Stathmin is a cytosolic phosphoprotein proposed to ac
t as a relay integrating diverse cell signalling pathways, notably during t
he control of cell growth and differentiation. it may also be considered as
one of the key regulators of cell division for its ability to destabilize
microtubules in a phosphorylation-dependent manner. To assess the significa
nce of stathmin overexpression in breast cancer, we evaluated the correlati
on of stathmin expression, quantified by reverse transcription polymerase c
hain reaction. with several disease parameters in a large series of human p
rimary breast cancer (n = 133), obtained in strictly followed up women, who
se clinico-pathological data were fully available. In agreement with our pr
eliminary survey, stathmin was found overexpressed in a subgroup of tumours
(22%). in addition, overexpression was correlated to the loss of steroid r
eceptors (oestrogen, P = 0.0006; progesterone, P = 0.008), and to the Scarf
f-Bloom-Richardson histopathological grade III (P = 0.002), this latter bei
ng ascribable to the mitotic index component (P = 0.02). Furthermore studie
s at the DNA level indicated that stathmin is overexpressed irrespective of
its genomic status. Our findings raise important questions concerning the
causes and consequences of stathmin overexpression, and the reasons of its
inability to counteract cell proliferation in the overexpression group. (C)
2000 Cancer Research Campaign.