EXPRESSION OF HEPATITIS-C VIRUS IN HEPATOCELLULAR-CARCINOMA

被引:0
作者
HARUNA, Y
HAYASHI, N
KAMADA, T
HYTIROGLOU, P
THUNG, SN
GERBER, MA
机构
[1] TULANE UNIV,SCH MED,DEPT PATHOL & LAB MED,NEW ORLEANS,LA 70112
[2] OSAKA UNIV,SCH MED,DEPT MED 1,SUITA,OSAKA 565,JAPAN
[3] MT SINAI SCH MED,LILLIAN & HENRY M STRATTON HANS POPPER DEPT P,NEW YORK,NY
关键词
HEPATITIS C VIRUS; HEPATOCELLULAR CARCINOMA; VIRAL REPLICATION; IMMUNOHISTOCHEMISTRY; POLYMERASE CHAIN REACTION;
D O I
10.1002/1097-0142(19940501)73:9<2253::AID-CNCR2820730904>3.0.CO;2-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Epidemiologic studies have suggested a strong association between chronic hepatitis C virus (HCV) infection and the development of hepatocellular carcinoma (HCC). To investigate the possible role of HCV in the pathobiology of HCC, the authors studied the expression of HCV in 10 cases of HCC with chronic HCV infection, Methods. The core, envelope, and nonstructural (NS) 3 and 5 proteins were localized in liver and tumor tissues by the immunoperoxidase technique using mouse monoclonal antibodies to recombinant proteins or synthetic peptide of HCV. In addition, the positive and negative strands of HCV RNA were detected in the tissues by strand-specific reverse transcription/double polymerase chain reaction using primers for the 5'-nontranslated region. Results. The HCV proteins were expressed in three of nine HCC specimens tested (the core protein in three HCC, the envelope, NS3 and NS5 proteins in one HCC) and in two of nine nontumorous liver specimens adjacent to the HCC (the core protein in two specimens, envelope, NS3 and NS5 proteins in one specimen). Positive-stranded HCV RNA was detected in all tumorous and nontumorous specimens except in one tumor. Negative-stranded HCV RNA was found in six of nine HCC tested and in all nontumorous livers. Conclusions. These findings suggest that HCV persists in hepatocytes during malignant transformation, although secondary infection of tumor cells by HCV cannot be excluded. Some HCC appear to support replication and expression of HCV,
引用
收藏
页码:2253 / 2258
页数:6
相关论文
共 30 条
[1]  
ALONSO MJ, 1992, EUR J HISTOCHEM, V36, P271
[2]  
AVANTAGGIATI ML, 1992, ARCH VIROL S, V4, P57
[3]  
BRUIX J, 1989, LANCET, V2, P1004
[4]   COEXPRESSION OF EPSTEIN-BARR-VIRUS LATENT MEMBRANE-PROTEIN AND VIMENTIN IN AGGRESSIVE HISTOLOGICAL SUBTYPES OF HODGKINS-DISEASE [J].
CARBONE, A ;
GLOGHINI, A ;
ZANETTE, I ;
CANAL, B ;
RIZZO, A ;
VOLPE, R .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1993, 422 (01) :39-45
[5]   EPSTEIN-BARR-VIRUS NUCLEAR PROTEIN-2 MUTATIONS DEFINE ESSENTIAL DOMAINS FOR TRANSFORMATION AND TRANSACTIVATION [J].
COHEN, JI ;
WANG, F ;
KIEFF, E .
JOURNAL OF VIROLOGY, 1991, 65 (05) :2545-2554
[6]   EPSTEIN-BARR-VIRUS NUCLEAR PROTEIN-2 IS A CRITICAL DETERMINANT FOR TUMOR-GROWTH IN SCID MICE AND FOR TRANSFORMATION INVITRO [J].
COHEN, JI ;
PICCHIO, GR ;
MOSIER, DE .
JOURNAL OF VIROLOGY, 1992, 66 (12) :7555-7559
[7]   DEGRADATION OF P53 CAN BE TARGETED BY HPV E6 SEQUENCES DISTINCT FROM THOSE REQUIRED FOR P53 BINDING AND TRANSACTIVATION [J].
CROOK, T ;
TIDY, JA ;
VOUSDEN, KH .
CELL, 1991, 67 (03) :547-556
[8]   EPSTEIN-BARR-VIRUS AND HODGKINS-DISEASE - TRANSCRIPTIONAL ANALYSIS OF VIRUS LATENCY IN THE MALIGNANT-CELLS [J].
DEACON, EM ;
PALLESEN, G ;
NIEDOBITEK, G ;
CROCKER, J ;
BROOKS, L ;
RICKINSON, AB ;
YOUNG, LS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (02) :339-349
[9]  
DIBISCEGLIE AM, 1991, AM J GASTROENTEROL, V86, P335
[10]   MORPHOLOGICAL TRANSFORMATION OF HUMAN KERATINOCYTES EXPRESSING THE LMP GENE OF EPSTEIN-BARR-VIRUS [J].
FAHRAEUS, R ;
RYMO, L ;
RHIM, JS ;
KLEIN, G .
NATURE, 1990, 345 (6274) :447-449