A. Bhuikaur et al., INCREASED PROSOMAL PROTEINS IN BREAST-CANCER CELLS AND IN NEIGHBORINGNORMAL-CELLS IN PARSI AND NON-PARSI POPULATIONS, Journal of cancer research and clinical oncology, 124(2), 1998, pp. 117-126
Monoclonal antibodies were raised against the prosomal proteins p27K,
p29K and the prosome-like protein p21K (PLP) from normal breast glandu
lar cells and from benign and malignant tumors. They were used to clar
ify the involvement of prosomes in tumorigenesis of human breast cells
. Immunostaining showed the distribution of prosomes in the cytoplasm
and nuclei of cells from European normal women (EN) and Parsi (P) and
non-Parsi (NP) benign (B) and malignant (M) tissues. The flow-cytometr
y studies showed an increased mean percentage of labeled cells, partic
ularly with anti-p27K prosomal protein mAb, in malignant tissue from N
P compared to EN. The p21K data indicated an increase in the number of
cells labeled by flow-cytometry studies in all groups compared to EN,
while p29K-expressing cells were more abundand in NPN, PB, PM and NPM
. Intergroup comparison showed that the mean percentage of cells label
ed with anti-p27K and anti-p29K was significantly higher in PB than in
NPB, as seen by flow cytometry, whereas there was a higher production
or accumulation of the p21K (PLP) prosomal protein in NPM than in PM,
as seen by immunostaining. By comparison with EN, there were also sig
nificantly more normal cells containing the three antigens in the appa
rently normal tissue in the neighborhood of the tumor in NPM, and more
cells containing p21K in PM patients than in EN. As prosomes are invo
lved in the cell differentiation and in the cell cycle control, the ch
anges observed in breast tissues may be related to oncogenic processes
. Furthermore, the modified subunit pattern of prosomes in cancer and,
possibly, pre-cancer tissue may be of interest for diagnosis purposes
.