The role of connexin-mediated cell-cell communication in breast cancer metastasis

被引:51
作者
Carystinos, GD
Bier, A
Batist, G
机构
[1] McGill Univ, Sir Mortimer B Davis Jewish Gen Hosp, Ctr Translat Res Canc, Dept Oncol, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Sir Mortimer B Davis Jewish Gen Hosp, Ctr Translat Res Canc, Dept Pharmacol & Therapeut, Montreal, PQ H3T 1E2, Canada
关键词
connexin; breast; metastasis; gap junction;
D O I
10.1023/A:1014787014851
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gap junctional intercellular communication (GJIC) is a form of cell-cell communication mediating the exchange of small molecules between neighboring cells. Gap junctions (GJs) are formed by connexins (Cxs), and are subject to tight and dynamic regulation. They are involved in the cell cycle, differentiation, and cell signaling. The loss of Cxs and GJs is a hallmark of carcinogenesis, while their induction in cancer cells leads to a reversal of the cancer phenotype, induction of differentiation, and regulation of cell growth. On the basis of the observations about Cx loss in breast cancer, this review examines Cxs' involvement in breast cancer metastasis. Previous work indicates that Cx expression is inversely correlated to metastatic potential. This is probably because of the loss of cooperation between neighboring cells, leading to cell heterogeneity and cell dissociation in the tumor. The possible involvement of Cx activity during metastasis will be discussed.
引用
收藏
页码:431 / 440
页数:10
相关论文
共 76 条
[1]  
ATKINSON MM, 1995, J CELL SCI, V108, P3079
[2]  
Bertram JS, 1999, NUTR REV, V57, P182, DOI 10.1111/j.1753-4887.1999.tb06941.x
[3]   CONNEXIN43 - A PROTEIN FROM RAT-HEART HOMOLOGOUS TO A GAP JUNCTION PROTEIN FROM LIVER [J].
BEYER, EC ;
PAUL, DL ;
GOODENOUGH, DA .
JOURNAL OF CELL BIOLOGY, 1987, 105 (06) :2621-2629
[4]   CELL-CULTURE ASSAYS FOR CHEMICALS WITH TUMOR-PROMOTING OR TUMOR-INHIBITING ACTIVITY-BASED ON THE MODULATION OF INTERCELLULAR COMMUNICATION [J].
BUDUNOVA, IV ;
WILLIAMS, GM .
CELL BIOLOGY AND TOXICOLOGY, 1994, 10 (02) :71-116
[5]  
CHEN SC, 1995, CELL GROWTH DIFFER, V6, P681
[6]   Signal transduction in mammary tumorigenesis: a transgenic perspective [J].
Dankort, DL ;
Muller, WJ .
ONCOGENE, 2000, 19 (08) :1038-1044
[7]  
deFeijter AW, 1996, MOL CARCINOGEN, V16, P203, DOI 10.1002/(SICI)1098-2744(199608)16:4<203::AID-MC4>3.3.CO
[8]  
2-F
[9]   GAP-JUNCTIONS IN THE BRAIN - WHERE, WHAT TYPE, HOW MANY AND WHY [J].
DERMIETZEL, R ;
SPRAY, DC .
TRENDS IN NEUROSCIENCES, 1993, 16 (05) :186-192
[10]   Differentiation of human fetal osteoblastic cells and gap junctional intercellular communication [J].
Donahue, HJ ;
Li, ZY ;
Zhou, ZY ;
Yellowley, CE .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2000, 278 (02) :C315-C322