The progression from normal breast epithelium to a malignant phenotype
may depend on changes in genetic events as well as failure of host me
chanisms. Intermediate biomarkers are needed to more effectively ident
ify malignant progression as well as to develop the potential for more
specific treatments and prevention strategies. The nuclear matrix is
the RNA-protein network which forms the skeleton of the nucleus and pa
rticipates in DNA organization as well as multiple cellular functions.
Nuclear matrix proteins have been demonstrated to be tissue and cell
type specific as well as to reflect the state of cell differentiation
and/or transformation. We prepared nuclear matrices from normal and ca
ncer breast tissue from 10 patients with infiltrating ductal carcinoma
of the breast as well as the MCF-10 mortal, immortal, and transfected
breast cell lines. Nuclear matrices derived from normal human breast
tissue and tumor tissue share common nuclear matrix proteins as well a
s demonstrate specific changes which appear to occur with the acquisit
ion of the cancer phenotype. The MCF-10 cell lines demonstrate a pheno
type that is intermediate between the normal and cancer tissue. These
data suggest that the nuclear matrix may be an important biomarker in
the pathogenesis of breast cancer.