Ra. Walker et B. Gallacher, DETERMINATION OF TRANSFORMING GROWTH-FACTOR BETA(1) MESSENGER-RNA EXPRESSION IN BREAST CARCINOMAS BY IN-SITU HYBRIDIZATION, Journal of pathology, 177(2), 1995, pp. 123-127
The expression of transforming growth factor beta, (TGF-beta(1)) mRNA
has been determined in 16 breast carcinomas using in situ hybridizatio
n and compared with TGF-beta protein as detected by antibodies against
TGF-beta(1), and TGF-beta(1), plus TGF-beta(2). Digoxigenin-labelled
riboprobes were used, with alkaline phosphatase and immunogold silver
detection systems. TGF-beta(1) mRNA was only detected in carcinomas in
which TGF-beta(1) protein was found (9 of 16 cases) and not in those
with prominent reactivity for TGF-beta(2). RNA. preservation was poor
in two other cases in which TGF-beta(1) protein had been detected. In
general, those tumours with greater numbers of cells labelled for TGF-
beta(1) mRNA had prominent reactivity for TGF-beta(1) protein. The mRN
A was localized to cancer cells with no labelling of stromal cells, al
though in a small number of cases scanty staining for TGF-beta(1) prot
ein had been observed in stromal cells. The incidence of detection of
TGF-beta(1), mRNA is lower than the published data from Northern analy
sis studies of breast carcinomas, suggesting that only higher levels o
f TGF-beta(1) mRNA expression are being detected by in situ hybridizat
ion. However, this approach has provided useful information about the
cellular sites of expression of TGF-beta(1) in breast carcinomas.