Abstract
A glycoprotein, termed amphiregulin (AR), inhibits growth of several human carcinoma cells in culture and stimulates proliferation of human fibroblasts and certain other tumor cells. It has been purified to apparent homogeneity from serum-free conditioned medium of MCF-7 human breast carcinoma cells that had been treated with phorbol 12-myristate 13-acetate. AR is a single-chain extremely hydrophilic glycoprotein containing cysteines in disulfide linkage(s) that are essential for biological activity; it is stable between pH 2 and pH 12 and after heating for 30 min at 56 degrees C but unstable at 100 degrees C. The apparent molecular weights of AR and N-Glycanase-treated AR are 14,000 and 15,000, respectively, as assessed by gel chromatography, and approximately 22,500 and approximately 14,000, respectively, as determined by polyacrylamide gel electrophoresis. Treatment of AR with N-Glycanase, O-Glycanase, or neuraminidase does not affect its activity. The pI of AR is approximately 7.8. The amino-terminal amino acid sequence of AR has been determined, and no significant sequence homology between AR and other proteins was found. The molecule thus appears to be a distinct growth regulatory protein.
MeSH Terms
Adenocarcinoma/metabolism
Amino Acid Sequence
Amphiregulin
Animals
Breast Neoplasms/metabolism
Cell Division/drug effects
Cell Line
DNA Replication/drug effects
EGF Family of Proteins
Glycoproteins/biosynthesis,isolation & purification,pharmacology
Growth Substances/biosynthesis,isolation & purification,pharmacology
Humans
Intercellular Signaling Peptides and Proteins
Molecular Sequence Data
Tetradecanoylphorbol Acetate/pharmacology
Chemicals
AREG protein, human
Amphiregulin
EGF Family of Proteins
Glycoproteins
Growth Substances
Intercellular Signaling Peptides and Proteins
Tetradecanoylphorbol Acetate
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shoyab M
Oncogen, Seattle, WA 98121.
McDonald V L
Bradley J G
Todaro G J
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