IS EPISIALIN MUC1 INVOLVED IN BREAST-CANCER PROGRESSION

被引:73
作者
HILKENS, J
VOS, HL
WESSELING, J
BOER, M
STORM, J
VANDERVALK, S
CALAFAT, J
PATRIARCA, C
机构
[1] Division of Tumor Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam
关键词
EPISIALIN; ADHESION; METASTASIS; CYTOTOXIC LYMPHOCYTES; BREAST CANCER;
D O I
10.1016/0304-3835(94)03674-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Episialin, also designated MUCl, CA 15-3 antigen and PEM, is an established serum marker for breast cancer. Its function and possible involvement in tumor progression has not yet been completely established. The molecule is an extended rod-like molecule protruding high above the cell surface. It is often highly overexpressed in breast cancer relative to normal breast epithelium cells. Overexpression of episialin on cells in vitro reduces cell-cell and cell-extracellular matrix adhesion, because the rod-like molecule masks the adhesion receptors. Episialin also exerts its antiadhesion effect in vivo. In certain human tumors, where episialin was present at the basal side of the cell, abnormal contacts between the plasma membrane and the stroma were observed. As a consequence of its anti-adhesion properties, episialin overexpression reduces the sensitivity of the cells for cytotoxic lymphocytes. This might be one of the reasons why episialin transfected cells are more potent to form experimental metastases after i.v. injection into nude mice.
引用
收藏
页码:27 / 33
页数:7
相关论文
共 22 条
[1]   DISSECTING TUMOR-CELL INVASION - EPITHELIAL-CELLS ACQUIRE INVASIVE PROPERTIES AFTER THE LOSS OF UVOMORULIN-MEDIATED CELL CELL-ADHESION [J].
BEHRENS, J ;
MAREEL, MM ;
VANROY, FM ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1989, 108 (06) :2435-2447
[2]   MONOCLONAL-ANTIBODY BRE-3 PARTICIPATION IN A MULTIVARIATE PROGNOSTIC MODEL FOR INFILTRATING DUCTAL CARCINOMA OF THE BREAST [J].
CHAN, CM ;
BARATTA, FS ;
OZZELLO, L ;
CERIANI, RL .
BREAST CANCER RESEARCH AND TREATMENT, 1994, 30 (03) :243-261
[3]  
CROGHAN GA, 1983, CANCER RES, V43, P4980
[4]  
FONTENOT JD, 1993, CANCER RES, V53, P5386
[5]  
GENDLER SJ, 1990, J BIOL CHEM, V265, P15286
[6]   PREDICTION OF PROGNOSIS IN PRIMARY BREAST-CANCER BY DETECTION OF A HIGH-MOLECULAR-WEIGHT MUCIN-LIKE ANTIGEN USING MONOCLONAL-ANTIBODIES DF3, F36/22, AND CU18 - A CANCER AND LEUKEMIA GROUP-B STUDY [J].
HAYES, DF ;
MESATEJADA, R ;
PAPSIDERO, LD ;
CROGHAN, GA ;
KORZUN, AH ;
NORTON, L ;
WOOD, W ;
STRAUCHEN, JA ;
GRIMES, M ;
WEISS, RB ;
REE, HJ ;
THOR, AD ;
KOERNER, FC ;
RICE, MA ;
BARCOS, M ;
KUFE, DW .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (07) :1113-1123
[7]   CELL MEMBRANE-ASSOCIATED MUCINS AND THEIR ADHESION-MODULATING PROPERTY [J].
HILKENS, J ;
LIGTENBERG, MJL ;
VOS, HL ;
LITVINOV, SV .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (09) :359-363
[8]  
HILKENS J, 1992, SEROLOGICAL CANC MAR, P261
[9]   WHY ARE PROTEINS O-GLYCOSYLATED [J].
JENTOFT, N .
TRENDS IN BIOCHEMICAL SCIENCES, 1990, 15 (08) :291-294
[10]   DIFFERENTIAL REACTIVITY OF A NOVEL MONOCLONAL-ANTIBODY (DF3) WITH HUMAN-MALIGNANT VERSUS BENIGN BREAST-TUMORS [J].
KUFE, D ;
INGHIRAMI, G ;
ABE, M ;
HAYES, D ;
JUSTIWHEELER, H ;
SCHLOM, J .
HYBRIDOMA, 1984, 3 (03) :223-232