RESPONSE TO AND EXPRESSION OF AMPHIREGULIN BY OVARIAN-CARCINOMA AND NORMAL OVARIAN SURFACE EPITHELIAL-CELLS - NUCLEAR-LOCALIZATION OF ENDOGENOUS AMPHIREGULIN

被引:93
作者
JOHNSON, GR
SAEKI, T
AUERSPERG, N
GORDON, AW
SHOYAB, M
SALOMON, DS
STROMBERG, K
机构
[1] NCI,TUMOR IMMUNOL & BIOL LAB,BETHESDA,MD 20892
[2] UNIV BRITISH COLUMBIA,DEPT ANAT,VANCOUVER V6T 1W5,BC,CANADA
[3] ONCOGEN,BRISTOL MYERS SQUIBB PHARMACEUT RES INST,SEATTLE,WA 98121
关键词
D O I
10.1016/S0006-291X(05)81090-3
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
Amphiregulin (AR) is a polypeptide growth regulator which has sequence homology to the epidermal growth factor-related family of ligands and contains putative nuclear targeting sequences. Human ovarian carcinoma cell lines and their normal counterparts, ovarian surface epithelial cells (OSEs), were assessed for their ability to respond to and express AR. Addition of exogenous AR (8-200 pM) inhibited the growth of 2 of 3 OSE specimens and 3 of the 6 carcinoma cell lines indicating that AR has the potential to inhibit the growth of normal cells, in addition to carcinoma cells. In contrast, concentrations of AR ranging from 1-5 nM stimulated the growth of all 3 of the OSEs and 4 of the 6 carcinoma cell lines. Immunocytochemical staining of the cells using antipeptide antibodies directed against residues 8-26 of AR indicated that all cells expressed AR and that the staining was localized to the nucleus. The nuclear staining of AR was concentrated in the nucleolus of the carcinoma cells, whereas the staining was diffuse in the nucleus of the OSEs. These results suggest that AR may play a growth regulatory role in the nucleus of cells and this role may be different in normal and malignant epithelial cells. © 1991 Academic Press, Inc.
引用
收藏
页码:481 / 488
页数:8
相关论文
共 20 条
  • [1] TRANSLOCATION OF BFGF TO THE NUCLEUS IS G1 PHASE CELL-CYCLE SPECIFIC IN BOVINE AORTIC ENDOTHELIAL-CELLS
    BALDIN, V
    ROMAN, AM
    BOSCBIERNE, I
    AMALRIC, F
    BOUCHE, G
    [J]. EMBO JOURNAL, 1990, 9 (05) : 1511 - 1517
  • [2] HIGH-AFFINITY EPIDERMAL GROWTH-FACTOR BINDING IS SPECIFICALLY REDUCED BY A MONOCLONAL-ANTIBODY, AND APPEARS NECESSARY FOR EARLY RESPONSES
    BELLOT, F
    MOOLENAAR, W
    KRIS, R
    MIRAKHUR, B
    VERLAAN, I
    ULLRICH, A
    SCHLESSINGER, J
    FELDER, S
    [J]. JOURNAL OF CELL BIOLOGY, 1990, 110 (02) : 491 - 502
  • [3] BASIC FIBROBLAST GROWTH-FACTOR ENTERS THE NUCLEOLUS AND STIMULATES THE TRANSCRIPTION OF RIBOSOMAL GENES IN ABAE CELLS UNDERGOING G0-]G1 TRANSITION
    BOUCHE, G
    GAS, N
    PRATS, H
    BALDIN, V
    TAUBER, JP
    TEISSIE, J
    AMALRIC, F
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (19) : 6770 - 6774
  • [4] THE ASSOCIATION OF POLYPEPTIDE HORMONES AND GROWTH-FACTORS WITH THE NUCLEI OF TARGET-CELLS
    BURWEN, SJ
    JONES, AL
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1987, 12 (04) : 159 - 162
  • [5] CIARDIELLO F, 1991, IN PRESS P NATL ACAD
  • [6] A HEPARIN SULFATE-REGULATED HUMAN KERATINOCYTE AUTOCRINE FACTOR IS SIMILAR OR IDENTICAL TO AMPHIREGULIN
    COOK, PW
    MATTOX, PA
    KEEBLE, WW
    PITTELKOW, MR
    PLOWMAN, GD
    SHOYAB, M
    ADELMAN, JP
    SHIPLEY, GD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (05) : 2547 - 2557
  • [7] SIGNAL TRANSDUCTION BY EPIDERMAL GROWTH-FACTOR OCCURS THROUGH THE SUBCLASS OF HIGH-AFFINITY RECEPTORS
    DEFIZE, LHK
    BOONSTRA, J
    MEISENHELDER, J
    KRUIJER, W
    TERTOOLEN, LGJ
    TILLY, BC
    HUNTER, T
    HENEGOUWEN, PMPV
    MOOLENAAR, WH
    DELAAT, SW
    [J]. JOURNAL OF CELL BIOLOGY, 1989, 109 (05) : 2495 - 2507
  • [8] ELLIOTT W M, 1990, Journal of Cell Biology, V111, p58A
  • [9] Harlow E., 1988, ANTIBODIES LAB MANUA, P53
  • [10] A HEPARIN-BINDING GROWTH-FACTOR SECRETED BY MACROPHAGE-LIKE CELLS THAT IS RELATED TO EGF
    HIGASHIYAMA, S
    ABRAHAM, JA
    MILLER, J
    FIDDES, JC
    KLAGSBRUN, M
    [J]. SCIENCE, 1991, 251 (4996) : 936 - 939