ANNULATE LAMELLAE IN A LARGE CELL LUNG-CARCINOMA CELL-LINE WITH HIGH EXPRESSION OF TYROSINE KINASE RECEPTOR AND PROTOONCOGENES

被引:15
作者
WANG, NS
LIU, C
EMOND, J
TSAO, MS
机构
[1] UNIV CALIF IRVINE,DEPT PATHOL,IRVINE,CA 92717
[2] MCGILL UNIV,MONTREAL GEN HOSP,MONTREAL H3G 1A4,QUEBEC,CANADA
关键词
ANNULATE LAMELLA; C-MET; TYROSINE; KINASE RECEPTORS;
D O I
10.3109/01913129209057829
中图分类号
TH742 [显微镜];
学科分类号
摘要
The morphology, karyotype, in vitro growth properties, and expression of tyrosine kinase receptors and proto-oncogenes are reported for a newly established large cell undifferentiated lung carcinoma cell line (RVH-6849). The results were analyzed concomitantly with those for two well established cell lines from an adenocarcinoma of the lung (A549) and a squamous cell carcinoma (A431). All three cell lines demonstrated common ultrastructural features of epithelial cells, but only RVH-6849 had frequent aggregates of centrioles and annulate lamellae (AL) and was polyploid, having five to seven copies of chromosome 7 by karyotype analysis. All three cell lines expressed transforming growth factor-alpha (TGF-alpha), epidermal growth factor receptor (EGFR), c-erb B-2, and c met genes. RVH-6849 cells, however, expressed the most messenger RNA (mRNA) for TGF-alpha, c-erb B-2, and c-met. Only EGFR mRNA was expressed more in the other two cell lines, especially in A431 cells-.AL represent an exaggerated form of the nuclear membrane pore complex that is found in actively proliferating cells such as germ and some neoplastic cells. AL are suspected to be involved in the deposition or processing of mRNA: The enhanced coexpression of AL and mRNAs of three tyrosine kinase containing receptors in RVH-6849 cells may represent such a relationship.
引用
收藏
页码:439 / 449
页数:11
相关论文
共 56 条
[1]   TUMOR PROMOTER AND EPIDERMAL GROWTH-FACTOR STIMULATE PHOSPHORYLATION OF THE C-ERBB-2-GENE PRODUCT IN MKN-7 HUMAN ADENOCARCINOMA CELLS [J].
AKIYAMA, T ;
SAITO, T ;
OGAWARA, H ;
TOYOSHIMA, K ;
YAMAMOTO, T .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (03) :1019-1026
[2]   MULTIPLE INDEPENDENT ACTIVATIONS OF THE NEU ONCOGENE BY A POINT MUTATION ALTERING THE TRANSMEMBRANE DOMAIN OF P185 [J].
BARGMANN, CI ;
HUNG, MC ;
WEINBERG, RA .
CELL, 1986, 45 (05) :649-657
[3]   CHARACTERIZATION OF THE STATE OF DIFFERENTIATION OF 6 NEWLY ESTABLISHED HUMAN NON-SMALL-CELL LUNG-CANCER CELL-LINES [J].
BEPLER, G ;
KOEHLER, A ;
KIEFER, P ;
HAVEMANN, K ;
BEISENHERZ, K ;
JAQUES, G ;
GROPP, C ;
HAEDER, M .
DIFFERENTIATION, 1988, 37 (02) :158-171
[4]  
BERCHUCK A, 1990, CANCER RES, V50, P4087
[5]   EPIDERMAL GROWTH-FACTOR RECEPTORS IN LUNG-TUMORS [J].
BERGER, MS ;
GULLICK, WJ ;
GREENFIELD, C ;
EVANS, S ;
ADDIS, BJ ;
WATERFIELD, MD .
JOURNAL OF PATHOLOGY, 1987, 152 (04) :297-307
[6]   EXPRESSION OF MULTIPLE GROWTH-FACTORS IN A HUMAN-LUNG CANCER CELL-LINE [J].
BETSHOLTZ, C ;
BERGH, J ;
BYWATER, M ;
PETTERSSON, M ;
JOHNSSON, A ;
HELDIN, CH ;
OHLSSON, R ;
KNOTT, TJ ;
SCOTT, J ;
BELL, GI ;
WESTERMARK, B .
INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (04) :502-507
[7]  
BIRRER MJ, 1988, SEMIN ONCOL, V15, P226
[8]  
BROWER M, 1986, CANCER RES, V46, P798
[9]  
BURHOLT DR, 1989, CANCER RES, V49, P3355
[10]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995