ROLE OF PROTEIN-KINASE C-ALPHA IN THE INDUCTION OF CARCINOEMBRYONIC ANTIGEN BY TRANSFORMING GROWTH-FACTOR-BETA-1

被引:15
作者
CHAKRABARTY, S
HUANG, S
机构
[1] Division of Laboratory Medicine, the University of Texas M.D. Anderson Cancer Center, Houston, Texas
关键词
D O I
10.1002/jcp.1041640119
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Previous studies showed that transforming growth factor beta 1 (TGF beta 1) regulates the expression of carcinoembryonic antigen (CEA) and CEA-cross-reactive glycoproteins (CEA-GLYs) in human colon carcinoma cells through a signal-transducing pathway associated with protein kinase C (PKC) (Chakrabarty, J. Cell. Physiol., 1992, 152:494-499). In this study we determined the role of the PKC alpha isoform in the regulation of CEA and CEA-GLYs expression by TGF beta 1. Expression of PKC alpha antisense RNA, through transfection experiments with an antisense PKC alpha expression vector, resulted in down-modulation of PKC alpha RNA and protein expression. TGF beta 1 was unable to stimulate the expression and secretion of CEA in cells in which the expression of PKC alpha protein was substantially reduced. The ability of TGF beta 1 to stimulate the expression of the 95- and 55-KDa CEA-GLYs, however, was not affected. We therefore conclude that TGF beta 1 regulates the secretion and expression of CEA through a signal-transducing pathway associated with PKC alpha. TGF beta 1 may also regulate the expression of CEA-GLYs through signal-transducing pathways associated with other PKC isoforms. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:148 / 153
页数:6
相关论文
共 39 条
[1]   IDENTIFICATION OF HUMAN ACTIVIN AND TGF-BETA TYPE-I RECEPTORS THAT FORM HETEROMERIC KINASE COMPLEXES WITH TYPE-II RECEPTORS [J].
ATTISANO, L ;
CARCAMO, J ;
VENTURA, F ;
WEIS, FMB ;
MASSAGUE, J ;
WRANA, JL .
CELL, 1993, 75 (04) :671-680
[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]   A TRANSFORMING GROWTH-FACTOR-BETA TYPE-I RECEPTOR THAT SIGNALS TO ACTIVATE GENE-EXPRESSION [J].
BASSING, CH ;
YINGLING, JM ;
HOWE, DJ ;
WANG, TW ;
HE, WW ;
GUSTAFSON, ML ;
SHAH, P ;
DONAHOE, PK ;
WANG, XF .
SCIENCE, 1994, 263 (5143) :87-89
[4]   TRANSREPRESSION OF TYPE-II COLLAGEN BY TGF-BETA AND FGF IS PROTEIN-KINASE-C DEPENDENT AND IS MEDIATED THROUGH REGULATORY SEQUENCES IN THE PROMOTER AND 1ST INTRON [J].
BRADHAM, DM ;
WIESCHE, BID ;
PRECHT, P ;
BALAKIR, R ;
HORTON, W .
JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 158 (01) :61-68
[5]  
CHAKRABARTY S, 1989, CANCER RES, V49, P2112
[6]  
CHAKRABARTY S, 1990, Molecular Biotherapy, V2, P27
[7]   ROLE OF PROTEIN-KINASE-C IN TRANSFORMING GROWTH FACTOR-BETA-1 INDUCTION OF CARCINOEMBRYONIC ANTIGEN IN HUMAN COLON-CARCINOMA CELLS [J].
CHAKRABARTY, S .
JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 152 (03) :494-499
[8]  
CHAKRABARTY S, 1988, CANCER RES, V48, P4059
[9]  
CHAKRABARTY S, 1990, INT J CANCER, V48, P493
[10]   THE TRANSFORMING GROWTH-FACTOR-BETA SYSTEM, A COMPLEX PATTERN OF CROSS-REACTIVE LIGANDS AND RECEPTORS [J].
CHEIFETZ, S ;
WEATHERBEE, JA ;
TSANG, MLS ;
ANDERSON, JK ;
MOLE, JE ;
LUCAS, R ;
MASSAGUE, J .
CELL, 1987, 48 (03) :409-415