Transforming growth factor (TGF) beta (1) is a growth factor with wide-rang
ing effects on proliferation, differentiation, immunosuppression, apoptosis
and matrix remodelling. TGF beta (1) seems to have an antitumorigenic role
in the gastrointestinal tract but may also be associated with the developm
ent of colorectal cancer. Initially, TGF beta (1) is produced in a latent (
precursor) form in epithelial cells and then is activated by a not clearly
understood multistep process. In this study, we analysed precursor TGF beta
(1) protein expression (n=40) and TGF beta (1) gene expression (n=49) in h
uman colorectal adenocarcinomas and 49 normal adjacent tissue. Out of these
49 normal tissues 40 were matched. Western blot analysis revealed that the
precursor TGF beta (1) protein levels were generally lower in colorectal c
ancerous tissue compared to adjacent noncancerous tissue (P <0.001). Furthe
rmore, with real-time PCR our results cannot reflect a statistically signif
icant difference in TGF beta (1) gene expression between the tumour tissue
and normal tissue. These finds indicate that it is likely that there are me
chanisms which control precursor TGF beta (1) protein expression by factor(
s) at the level of pre-translation of the TGF beta (1) transcript and/or at
the level of post-translation of the TGF beta (1) protein in the tumours.
This process may be related to carcinogenesis and poses the question whethe
r the suppression of the precursor TGF beta (1) is an early event, in vivo,
in the human colorectal adenoma-carcinoma sequence.