The loss of expression of transforming growth factor-beta receptors correlates with the histopathologic tumor grade in bladder transitional cell carcinoma patients

Citation
Dh. Lee et al., The loss of expression of transforming growth factor-beta receptors correlates with the histopathologic tumor grade in bladder transitional cell carcinoma patients, YONSEI MED, 40(2), 1999, pp. 118-123
Citations number
25
Categorie Soggetti
General & Internal Medicine
Journal title
YONSEI MEDICAL JOURNAL
ISSN journal
05135796 → ACNP
Volume
40
Issue
2
Year of publication
1999
Pages
118 - 123
Database
ISI
SICI code
0513-5796(199904)40:2<118:TLOEOT>2.0.ZU;2-L
Abstract
Transforming growth factor-beta (TGF-beta), a pleiotropic growth factor, is a potent inhibitor of cellular proliferation in cells of epithelial origin . Recently, it has been suggested chat a loss of sensitivity to TGF-beta th rough a loss of expression of TGF-beta receptors T beta R-I and T beta R-II - is associated with tumor initiation and progression. Therefore, ro inves tigate the relationship between TGF-beta receptors expression and carcinoge nesis of bladder TCC, this study examined the expression of T beta R-I and T beta R-II in 46 bladder TCC patients using immunohistochemistry. Since hi stopathological grade is a widely accepted marker of prognosis, the results were compared in relation to the three grades of bladder TCC. The results demonstrated that the loss of TGF-beta receptors expression is associated w ith increasing histopathological grades of bladder TCC. Specifically, both T beta R-I and T beta R-II were readily detected in all 10 normal bladder m ucosa specimens. Likewise, all 6 specimens of grade I TCC samples expressed high levels of both TGF-beta receptors. However, among grade II TCC sample s, T beta R-I and T beta R-II were detected in 78% and 89%, respectively: a mong grade III TCC samples, T beta R-I and T beta R-II were detected in 45% and 41%, respectively. These results suggested that loss of sensitivity to TGF-beta may play a role in the progression of TCC from low to high grade disease.