In situ nucleic acid detection of human telomerase in intrahepatic cholangiocarcinoma and its preneoplastic lesion

Citation
S. Ozaki et al., In situ nucleic acid detection of human telomerase in intrahepatic cholangiocarcinoma and its preneoplastic lesion, HEPATOLOGY, 30(4), 1999, pp. 914-919
Citations number
26
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
HEPATOLOGY
ISSN journal
02709139 → ACNP
Volume
30
Issue
4
Year of publication
1999
Pages
914 - 919
Database
ISI
SICI code
0270-9139(199910)30:4<914:ISNADO>2.0.ZU;2-5
Abstract
Human telomerase, an enzyme associated with cellular immortality and tumori genesis, is expressed by most malignant tumor cells. Human telomerase consi sts of human telomerase RNA (hTR) and telomerase protein components. One of the latter has been cloned and was termed telomerase-associated protein 1 (TP1), Using an in situ hybridization method, expression of hTR and TP1 mRN A was surveyed in 20 cases of intrahepatic cholangiocarcinoma (ICC) (5 of t hem were associated with hepatolithiasis), 5 cases of hepatolithiasis alone and 6 normal livers. Biliary dysplasia, which is suspected as a preneoplas tic lesion of ICC, was found in the biliary tree in all 5 ICC cases with he patolithiasis and in 1 of 5 cases of hepatolithiasis alone, Normal colonic mucosa was used as positive control. In 17 (85%) of 20 ICC cases, hTR and T P1 mRNA were detected in carcinoma cells. There was no correlation between histological subtype of ICC and expression of hTR and TP1 mRNA. Biliary dys plasia was also positive for both RNA. These signals were mainly located in the cytoplasm of carcinoma and dysplastic cells, especially around their n uclei, The signals were homogeneously detected in the carcinoma, while thei r distribution was more or less heterogeneous in the dysplastic foci. These signals were not detected in nondysplastic biliary epithelia in hepatolith iasis and normal livers. It seems likely that almost all ICC acquired telom erase activities irrespective of histological subtype and more importantly that cellular immortalization has already occurred in biliary dysplasia and this lesion is already involved in the malignant progression of ICC.