Reduced connexin 43 expression in high grade, human prostatic adenocarcinoma cells

被引:93
作者
Tsai, H
Werber, J
Davia, MO
Edelman, M
Tanaka, KE
Melman, A
Christ, GJ
Geliebter, J
机构
[1] MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT UROL,BRONX,NY 10461
[2] MONTEFIORE MED CTR,ALBERT EINSTEIN COLL MED,DEPT PATHOL,BRONX,NY 10461
关键词
D O I
10.1006/bbrc.1996.1468
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gap junction-mediated communication is required for normal cellular growth and differentiation. As cancer is thought to be a manifestation of the breakdown of cell-cell communication, with the concomitant loss of growth control, it would be expected that alterations in the primary structure, processing, oligomerization or trafficking of connexin (cxn) molecules would have a profound effect an the neoplastic process. Here we a present a preliminary immunohistochemical and molecular analysis of cxn 43 expression in prostatic epithelial cells from resected human tissue. Our data indicate that benign prostatic epithelial cells express cxn 43 protein, but that this expression is diminished in more advanced, anaplastic cancer cells. These data suggest that decreased connexin expression is not involved in the initiation of prostate cancer, but rather occurs during the progression of the disease. (C) 1996 Academic Press, Inc.
引用
收藏
页码:64 / 69
页数:6
相关论文
共 14 条
[1]   ALTERATION IN EXPRESSION OF GAP JUNCTION PROTEINS IN RAT-LIVER AFTER TREATMENT WITH THE TUMOR PROMOTER 3,4,5,3',4'-PENTACHLOROBIPHENYL [J].
BAGER, Y ;
KENNE, K ;
KRUTOVSKIKH, V ;
MESNIL, M ;
TRAUB, O ;
WARNGARD, L .
CARCINOGENESIS, 1994, 15 (11) :2439-2443
[2]   INVOLVEMENT OF GAP-JUNCTIONS IN TUMORIGENESIS - TRANSFECTION OF TUMOR-CELLS WITH CONNEXIN-32 CDNA RETARDS GROWTH-INVIVO [J].
EGHBALI, B ;
KESSLER, JA ;
REID, LM ;
ROY, C ;
SPRAY, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) :10701-10705
[3]   THE HUMAN CONNEXIN GENE FAMILY OF GAP JUNCTION PROTEINS - DISTINCT CHROMOSOMAL LOCATIONS BUT SIMILAR STRUCTURES [J].
FISHMAN, GI ;
EDDY, RL ;
SHOWS, TB ;
ROSENTHAL, L ;
LEINWAND, LA .
GENOMICS, 1991, 10 (01) :250-256
[4]   EXPRESSION AND FUNCTION OF CONNEXIN IN NORMAL AND TRANSFORMED HUMAN KERATINOCYTES IN CULTURE [J].
FITZGERALD, DJ ;
FUSENIG, NE ;
BOUKAMP, P ;
PICCOLI, C ;
MESNIL, M ;
YAMASAKI, H .
CARCINOGENESIS, 1994, 15 (09) :1859-1865
[5]   INTERACTION BETWEEN KB AND Q4 GENE-SEQUENCES GENERATES THE KBM6 MUTATION [J].
GELIEBTER, J ;
ZEFF, RA ;
SCHULZE, DH ;
PEASE, LR ;
WEISS, EH ;
MELLOR, AL ;
FLAVELL, RA ;
NATHENSON, SG .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (02) :645-652
[6]  
GROSSMAN HB, 1994, CANCER RES, V54, P3062
[7]  
HOTZWAGENBLATT A, 1993, CRIT REV ONCOGENESIS, V4, P541
[8]  
KRUTOVSKIKH V, 1994, INT J CANCER, V56, P87
[9]   DIFFERENTIAL EXPRESSION OF GAP JUNCTION CONNEXINS IN ENDOCRINE AND EXOCRINE GLANDS [J].
MEDA, P ;
PEPPER, MS ;
TRAUB, O ;
WILLECKE, K ;
GROS, D ;
BEYER, E ;
NICHOLSON, B ;
PAUL, D ;
ORCI, L .
ENDOCRINOLOGY, 1993, 133 (05) :2371-2378
[10]   POSSIBLE MOLECULAR MECHANISM OF LOSS OF HOMOLOGOUS AND HETEROLOGOUS GAP JUNCTIONAL INTERCELLULAR COMMUNICATION IN RAT-LIVER EPITHELIAL-CELL LINES [J].
MESNIL, M ;
ASAMOTO, M ;
PICCOLI, C ;
YAMASAKI, H .
CELL ADHESION AND COMMUNICATION, 1994, 2 (05) :377-384