The ductal carcinoma in situ (DCIS) of the mammary gland represents an earl
y, pre-invasive stage in the development of invasive breast carcinoma and i
s increasingly diagnosed since the introduction of high-quality mammography
screening. Uncertainties in the prognosis for patients with DCIS have caus
ed a controversial discussion about adequate treatment, and it is suspected
that most patients undergoing mastectomy may be overtreated, In order to i
mprove treatment and treatment decision, it therefore is highly desirable t
o identify prognostic markers and therapeutic targets for DCIS. We here int
roduce a set of transgenic mice (WAP-T and WAP-T-NP lines) presenting with
various morphological forms of DCLS-like lesions. In these mite the SV40 la
rge tumor antigen is specifically induced in epithelial cells of the termin
al duct lobular units (TDLU), As a consequence of continuous expression of
the oncogene, the animals develop multifocal DCIS and consequently invasive
carcinoma within strain specific periods of latency. DCIS lesions in trans
genic mire exhibit distinct architectural and cytological features which cl
osely resemble those commonly present in humans, We therefore propose these
transgenic lines as an experimental model to study the underlying molecula
r events leading to DCIS and its progression to invasive disease.