TENASCIN IN INFLAMMATORY CONDITIONS AND NEOPLASMS OF THE URINARY-BLADDER

Citation
O. Tiitta et al., TENASCIN IN INFLAMMATORY CONDITIONS AND NEOPLASMS OF THE URINARY-BLADDER, Virchows Archiv including cell pathology including molecular pathology, 63(5), 1993, pp. 283-287
Citations number
32
Categorie Soggetti
Cytology & Histology",Pathology
Volume
63
Issue
5
Year of publication
1993
Pages
283 - 287
Database
ISI
SICI code
Abstract
Tenascin (Tn) is an extracellular matrix (ECM) glycoprotein strongly a nd widely expressed during embryogenesis. Tn is decreased in normal ad ult tissues but is reexpressed in numerous inflammatory, reparative an d neoplastic processes. We immunostained samples of fetal and normal a dult bladders and samples of bladder tissue from patients with chronic cystitis, detrusor hypertrophy, malakoplakia and transitional cell ca rcinomas (TCC) of all grades, with a monoclonal antibody (mAb) to Tn 1 43DB7. Sections of flat in situ carcinomas were also studied. In fetal bladders, strong and ragged Tn reactions were noted at the epithelial -stromal interface; in normal adult bladders, the reaction was delicat e and less extensive. In chronic cystitis, Tn reactivity was enhanced particularly around prominent capillary blood vessels. In flat in situ carcinomas, Tn staining was stronger and more extensive than in norma l mucosa but was often less extensive than in some examples of cystiti s. In TCC I and II, Tn immunoreactivity was strong and predominated in the pericapillary stroma of the papillae; in infiltrating TCC II, com paratively limited Tn staining was noted. In deeply infiltrating grade III TCC with abundant stroma, Tn reaction was invariably strong and e xtensive, particularly around advancing tumor nests. The strongest Tn reactions were noted in invasive, high-grade TCC with abundant stroma. We conclude that in inflammatory-reactive processes, and in in situ c arcinomas as well as in TCC, the extent and intensity of the Tn reacti on correlates with the severity of the inflammatory infiltrate and wit h the extent of the stromal remodelling.