THE ROLE OF GAP JUNCTIONAL INTERCELLULAR COMMUNICATION IN NEOPLASIA

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RUCH, RJ
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R446 [实验室诊断]; R-33 [实验医学、医学实验];
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1001 ;
摘要
Gap junctions are comprised of proteinaceous, plasma membrane channels that link the interiors of adjacent cells and permit cells to directly exchange small (<1,000 Daltons) molecules and ions. This exchange, termed gap junctional intercellular communication (GJIC), appears to be involved in growth regulation. Growth controlling factors may pass between cells through the junctions. The loss of gap junctions or impairment of their permeability has been observed in many neoplastic cells and cells treated with growth promoting carcinogens and other agents. The loss of GJIG appears to be an important event in the conversion of a normal cell into a neoplastic one. On the other hand, the restoration of GJIC in neoplastic cells by transfection with gap junction protein (connexin) cyclic deoxyribonucleic acids (cDNAs) or by stimulating endogenous connexin gene expression has led to the reversal of the neoplastic phenotype. The biology of gap junctions and their role in growth regulation and neoplasia are reviewed.
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页码:216 / 231
页数:16
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共 58 条
[1]   RAPID AND REVERSIBLE REDUCTION OF JUNCTIONAL PERMEABILITY IN CELLS INFECTED WITH A TEMPERATURE-SENSITIVE MUTANT OF AVIAN-SARCOMA VIRUS [J].
ATKINSON, MM ;
MENKO, AS ;
JOHNSON, RG ;
SHEPPARD, JR ;
SHERIDAN, JD .
JOURNAL OF CELL BIOLOGY, 1981, 91 (02) :573-578
[2]   INTERCELLULAR COMMUNICATION AND THE CONTROL OF GROWTH .10. ALTERATION OF JUNCTIONAL PERMEABILITY BY THE SRC GENE - A STUDY WITH TEMPERATURE-SENSITIVE MUTANT ROUS-SARCOMA VIRUS [J].
AZARNIA, R ;
LOEWENSTEIN, WR .
JOURNAL OF MEMBRANE BIOLOGY, 1984, 82 (03) :191-205
[3]  
BERTHOUD VM, 1992, EUR J CELL BIOL, V57, P40
[4]   THE TUMOR PROMOTER 12-O-TETRADECANOYLPHORBOL-13-ACETATE AND THE RAS ONCOGENE MODULATE EXPRESSION AND PHOSPHORYLATION OF GAP JUNCTION PROTEINS [J].
BRISSETTE, JL ;
KUMAR, NM ;
GILULA, NB ;
DOTTO, GP .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (10) :5364-5371
[5]   GAP JUNCTIONAL INTERCELLULAR COMMUNICATION IN MOUSE LUNG EPITHELIAL-CELL LINES - EFFECTS OF CELL-TRANSFORMATION AND TUMOR PROMOTERS [J].
CHAUDHURI, R ;
SIGLER, K ;
DUPONT, E ;
TROSKO, JE ;
MALKINSON, AM ;
RUCH, RJ .
CANCER LETTERS, 1993, 71 (1-3) :11-18
[6]   PHOSPHORYLATION OF CONNEXIN43 GAP JUNCTION PROTEIN IN UNINFECTED AND ROUS-SARCOMA VIRUS-TRANSFORMED MAMMALIAN FIBROBLASTS [J].
CROW, DS ;
BEYER, EC ;
PAUL, DL ;
KOBE, SS ;
LAU, AF .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (04) :1754-1763
[7]   MAJOR LOSS OF THE 28-KD PROTEIN OF GAP JUNCTION IN PROLIFERATING HEPATOCYTES [J].
DERMIETZEL, R ;
YANCEY, SB ;
TRAUB, O ;
WILLECKE, K ;
REVEL, JP .
JOURNAL OF CELL BIOLOGY, 1987, 105 (04) :1925-1934
[8]   MORPHOREGULATORY MOLECULES [J].
EDELMAN, GM .
BIOCHEMISTRY, 1988, 27 (10) :3533-3543
[9]   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
[10]  
ELVIRA M, 1993, J BIOL CHEM, V268, P14294