Expressions of h-TERT, c-myc, PCNA and cell apoptosis in liver carcinogenesis.
- Author:
Xiao-mei FU
1
;
Qing-xu YANG
;
Chun-kui SHAO
;
Zhi-ying FENG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Apoptosis; Carcinoma, Hepatocellular; genetics; metabolism; pathology; Cell Transformation, Neoplastic; Female; Hepatitis B, Chronic; genetics; metabolism; pathology; Humans; Immunohistochemistry; Liver Cirrhosis; genetics; metabolism; pathology; Liver Neoplasms; genetics; metabolism; pathology; Male; Middle Aged; Proliferating Cell Nuclear Antigen; biosynthesis; Proto-Oncogene Proteins c-myc; genetics; RNA, Messenger; genetics; metabolism; Telomerase; genetics
- From: Journal of Southern Medical University 2006;26(6):821-823
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the expressions of human telomerase reverse transcriptase (h-TERT), c-myc, and proliferating cell nuclear antigen (PCNA) in chronic viral hepatitis (CVH), liver cirrhosis and primary hepatocellular carcinoma (HCC) and understand their possible role in liver carcinogenesis.
METHODSTotally 157 liver disease specimens were collected, including 56 CVH, 52 liver cirrhosis and 49 primary HCC specimens. In situ hybridization was performed on these specimens to examine the expressions of h-TRET and c-myc mRNA, and immunohistochemistry carried out for PCNA detection, with the cell apoptosis detected with in situ ending labeling.
RESULTSIn the CVH, liver cirrhosis and primary HCC specimens, h-TERT expression was detected at the frequencies of 11/56 (19.6%), 43/52 (82.7%) and 44/47 (93.6%), c-myc expression at 7/56 (12.5%), 21/52 (40.4%) and 26/47 (55.3%), with apoptotic index of (27.3-/+4.7)%, (16.5-/+2.6)% and (8.7-/+1.3)% and PCNA expression rate of (17.1-/+2.9)%, (49.3-/+7.8)% and (62.5-/+9.1)%, respectively. Correlations among h-TERT, c-myc, and PCNA expressions and the apoptotic index were not found in the examined tissues (P>0.05).
CONCLUSIONLiver carcinogenesis may involve increased h-TERT, c-myc, and PCNA expressions and suppressed cell apoptosis.