Home LiteratureArticle Details
PMID: 1311287 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Analysis of tyrosine kinase mRNAs including four FGF receptor mRNAs expressed in MCF-7 breast-cancer cells.

International journal of cancer ·Vol. 50 ·No. 4 ·1992-02-20 ·Pages 598-603

Lehtola L, Partanen J, Sistonen L, Korhonen J, Wärri A, Härkönen P, Clarke R, Alitalo K

Abstract

The MCF-7 cell line is a hormone-responsive human breast-cancer cell line, which has been extensively used in studies of estrogen regulation of cell growth. These studies have indicated that the growth stimulation of the MCF-7 cells by estrogens may be effected by an autocrine mechanism involving several growth factors, such as EGF, TGF alpha and IGF-I and their receptors. We have amplified and cloned tyrosine-kinase-related sequences from the MCF-7 cell mRNA using the polymerase chain reaction and characterized the partial cDNAs obtained by nucleic acid sequencing. Nine tyrosine kinase cDNAs and one serine/threonine kinase cDNA were identified among the amplified sequences. Four different tyrosine kinase genes encoding receptors for fibroblast growth factors (FGFs) were found to be expressed by the MCF-7 cells. In addition, differences were observed in the expression of these members of FGF receptor family in different breast-cancer cells. A putative tyrosine-kinase receptor and a novel serine/threonine kinase were preferentially expressed in estrogen-responsive tumor cell lines. However, no estrogen-dependent regulation of any of the novel tyrosine-kinase receptor mRNAs was found in any of the cell lines including the MCF-7 or ZR-75-I cells, where the expression of the neu proto-oncogene mRNA was decreased during estrogen treatment. The expression of several FGF receptors by breast-cancer cells suggests that FGFs may be involved in their growth regulation and tumorigenesis.

Related Genes
MeSH Terms
Amino Acid Sequence Base Sequence Breast Neoplasms/genetics Cloning, Molecular Gene Expression Gene Expression Regulation, Neoplastic/drug effects Humans Molecular Sequence Data Oligodeoxyribonucleotides/chemistry Polymerase Chain Reaction Protein Kinase C/genetics Protein Kinases/genetics Protein Serine-Threonine Kinases Protein-Tyrosine Kinases/genetics Proto-Oncogene Mas RNA, Messenger/genetics RNA, Neoplasm/genetics Receptors, Cell Surface/genetics Receptors, Fibroblast Growth Factor Sequence Alignment Steroids/pharmacology Tumor Cells, Cultured
Chemicals
MAS1 protein, human Oligodeoxyribonucleotides Proto-Oncogene Mas RNA, Messenger RNA, Neoplasm Receptors, Cell Surface Receptors, Fibroblast Growth Factor Steroids Protein Kinases Protein-Tyrosine Kinases Protein Serine-Threonine Kinases Protein Kinase C
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Lehtola L
Department of Pathology, University of Helsinki, Finland.
Partanen J
Sistonen L
Korhonen J
Wärri A
Härkönen P
Clarke R
Alitalo K
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1992-02-20
Pages
598-603
Language
English
Region
United States
NLM ID
0042124
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com