TRANSCRIPTION OF BILIARY GLYCOPROTEIN-I GENE IN MALIGNANT AND NONMALIGNANT HUMAN LIVER-TISSUES

被引：32

作者：

HINODA, Y ^{[1
]}

IMAI, K ^{[1
]}

NAKAGAWA, N ^{[1
]}

IBAYASHI, Y ^{[1
]}

NAKANO, T ^{[1
]}

PAXTON, RJ ^{[1
]}

SHIVELY, JE ^{[1
]}

YACHI, A ^{[1
]}

机构：

[1] CITY HOPE NATL MED CTR,BECKMAN RES INT,DIV IMMUNOL,DUARTE,CA 91010

来源：

INTERNATIONAL JOURNAL OF CANCER | 1990年 / 45卷 / 05期

关键词：

D O I：

10.1002/ijc.2910450516

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Biliary glycoprotein I (BGP I) is a member of carcinoembryonic antigen (CEA) gene family consisting of at least II related genes. The transcription of BGP I gene was analysed in malignant and non‐malignant human liver tissues with a 396‐bp 3′‐untranslated region probe from a cDNA clone 4‐13 which was newly isolated from an adult human colon cDNA library. Among 21 tissue samples from 14 patients with hepatocellular carcinoma, 16 samples were clearly shown to express a single 3.9‐kb message. This message was also found in the hepatoma cell line HuH‐7. When the malignant tissues were compared to the non‐malignant ones for the intensity of the band, no significant difference was observed. mRNAs of CEA and non‐specific cross‐reacting antigen (NCA) were not detected in 5 samples which were shown to have the message of the BGP I gene. These data suggest that the human hepatocyte and its malignant transformant produce BGP I, and that this could correspond to the cross‐reacting antigen previously detected in the liver. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company

引用

页码：875 / 878

页数：4

共 21 条

[1] GENERATION OF PROTEIN ISOFORM DIVERSITY BY ALTERNATIVE SPLICING - MECHANISTIC AND BIOLOGICAL IMPLICATIONS [J].

ANDREADIS, A ;

GALLEGO, ME ;

NADALGINARD, B .

ANNUAL REVIEW OF CELL BIOLOGY, 1987, 3 :207-242

[2] CARCINOEMBRYONIC ANTIGENS - ALTERNATIVE SPLICING ACCOUNTS FOR THE MULTIPLE MESSENGER-RNAS THAT CODE FOR NOVEL MEMBERS OF THE CARCINOEMBRYONIC ANTIGEN FAMILY [J].

BARNETT, TR ;

KRETSCHMER, A ;

AUSTEN, DA ;

GOEBEL, SJ ;

HART, JT ;

ELTING, JJ ;

KAMARCK, ME .

JOURNAL OF CELL BIOLOGY, 1989, 108 (02) :267-276

[3] ISOLATION AND CHARACTERIZATION OF FULL-LENGTH FUNCTIONAL CDNA CLONES FOR HUMAN CARCINOEMBRYONIC ANTIGEN [J].

BEAUCHEMIN, N ;

BENCHIMOL, S ;

COURNOYER, D ;

FUKS, A ;

STANNERS, CP .

MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (09) :3221-3230

[4]

COURNOYER D, 1988, CANCER RES, V48, P3153

[5]

DAVIS LG, 1986, BASIC METHODS MOL BI, P130

[6]

ENDO Y, 1979, CARCINOEMBRYONIC PRO, V1, P91

[7]

HINODA Y, 1989, P NATL ACAD SCI USA, V86, P1668

[8] MOLECULAR-CLONING OF A CDNA CODING BILIARY GLYCOPROTEIN-I - PRIMARY STRUCTURE OF A GLYCOPROTEIN IMMUNOLOGICALLY CROSSREACTIVE WITH CARCINOEMBRYONIC ANTIGEN [J].

HINODA, Y ;

NEUMAIER, M ;

HEFTA, SA ;

DRZENIEK, Z ;

WAGENER, C ;

SHIVELY, L ;

HEFTA, LJF ;

SHIVELY, JE ;

PAXTON, RJ .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6959-6963

[9]

HIROHASHI S, 1983, JAP J ONCOL, V143, P37

[10]

KODAMA T, 1979, CARCINOEMBRYONIC PRO, V2, P93

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