MECHANISMS OF P185(HER2) EXPRESSION IN HUMAN NON-SMALL-CELL LUNG-CANCER CELL-LINES

被引:43
作者
KERN, JA
ROBINSON, RA
GAZDAR, A
TORNEY, L
WEINER, DB
机构
[1] UNIV IOWA,COLL MED,DEPT PATHOL,IOWA CITY,IA 52242
[2] UNIV PENN,SCH MED,DEPT MED,PHILADELPHIA,PA 19104
[3] UNIV PENN,SCH MED,DEPT PATHOL & LAB MED,PHILADELPHIA,PA 19104
[4] NCI,BETHESDA,MD 20892
[5] USN HOSP,BETHESDA,MD 20814
关键词
D O I
10.1165/ajrcmb/6.4.359
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
To identify mechanisms that allow p185HER2 expression in lung cancer, we performed Western, Southern, and Northern blot analyses of 14 cell lines derived from human non-small cell lung carcinomas and one cell line derived from a human mesothelioma. Human bronchiole epithelial cells and rat type II pneumocytes were found to express p185HER2 at low to undetectable levels by Western blot technique. In contrast, 13 lung cancer cell lines expressed p185HER2, and eight of these 13 expressed p185HER2 at levels at least 2-fold higher than that found in normal bronchiole epithelial cells or type II pneumocytes. Genomic Southern analysis showed that amplification of the HER2 gene was present in only one of the eight cell lines that expressed p185HER2 at these higher levels. Increased levels of steady-state HER2 mRNA occurred in the remaining seven cell lines. We conclude that in human non-small cell lung carcinoma cell lines the most common mechanism resulting in increased p185HER2 expression is due to mechanisms that increase HER2 mRNA levels, with HER2 gene amplification occurring less commonly.
引用
收藏
页码:359 / 363
页数:5
相关论文
共 24 条
  • [1] THE PRODUCT OF THE HUMAN C-ERBB-2 GENE - A 185-KILODALTON GLYCOPROTEIN WITH TYROSINE KINASE-ACTIVITY
    AKIYAMA, T
    SUDO, C
    OGAWARA, H
    TOYOSHIMA, K
    YAMAMOTO, T
    [J]. SCIENCE, 1986, 232 (4758) : 1644 - 1646
  • [2] BARGMANN CI, 1986, NATURE, V319, P225
  • [3] BERGER MS, 1988, CANCER RES, V48, P1238
  • [4] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [5] NUMBER AND EVOLUTIONARY CONSERVATION OF ALPHA-TUBULIN AND BETA-TUBULIN AND CYTOPLASMIC BETA-ACTIN AND GAMMA-ACTIN GENES USING SPECIFIC CLONED CDNA PROBES
    CLEVELAND, DW
    LOPATA, MA
    MACDONALD, RJ
    COWAN, NJ
    RUTTER, WJ
    KIRSCHNER, MW
    [J]. CELL, 1980, 20 (01) : 95 - 105
  • [6] CLINE MJ, 1987, CANCER, V60, P2669, DOI 10.1002/1097-0142(19871201)60:11<2669::AID-CNCR2820601116>3.0.CO
  • [7] 2-4
  • [8] COHEN JA, 1989, ONCOGENE, V4, P81
  • [9] DAVIS LG, 1986, BASIC METHODS MOL BI, P44
  • [10] DOBBS LG, 1986, AM REV RESPIR DIS, V134, P141