Many attempts are made to identify critical genetic events responsible for
the development and progression of breast cancer. There is increasing evide
nce that breast cancer is a heterogeneous disease, both, phenotypically as
well as with respect to its molecular biologically. It is, therefore, extre
mely difficult to establish a diagnostically and prognostically relevant tu
mourigenesis model. Emerging new techniques such as microarrays, will provi
de us with a wealth of additional data over the next years. The precise sam
pling of tumour material in clearly defined histopathological lesions will
be a prerequisite for the assignment of specific genetic alterations to def
ined stages of breast disease.