Decreased levels of precursor transforming growth factor beta(1) in human colorectal cancer

Citation
J. Dimberg et al., Decreased levels of precursor transforming growth factor beta(1) in human colorectal cancer, INT J MOL M, 7(6), 2001, pp. 597-601
Citations number
24
Categorie Soggetti
Medical Research General Topics
Journal title
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
ISSN journal
11073756 → ACNP
Volume
7
Issue
6
Year of publication
2001
Pages
597 - 601
Database
ISI
SICI code
1107-3756(200106)7:6<597:DLOPTG>2.0.ZU;2-P
Abstract
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.