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PMID: 9449709 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of the Elm1 gene, a novel gene of the CCN (connective tissue growth factor, Cyr61/Cef10, and neuroblastoma overexpressed gene) family, suppresses In vivo tumor growth and metastasis of K-1735 murine melanoma cells.

The Journal of experimental medicine ·Vol. 187 ·No. 3 ·1998-02-02 ·Pages 289-96

Hashimoto Y, Shindo-Okada N, Tani M, Nagamachi Y, Takeuchi K, Shiroishi T, Toma H, Yokota J

Abstract

We previously isolated a partial cDNA fragment of a novel gene, Elm1 (expressed in low-metastatic cells), that is expressed in low-metastatic but not in high-metastatic K-1735 mouse melanoma cells. Here we determined the full-length cDNA structure of Elm1 and investigated the effect of Elm1 expression on growth and metastatic potential of K-1735 cells. The Elm1 gene encodes a predicted protein of 367 amino acids showing approximately 40% amino acid identity with the CCN (connective tissue growth factor [CTGF], Cyr61/Cef10, neuroblastoma overexpressed gene [Nov]) family proteins, which consist of secreted cysteine-rich proteins with growth regulatory functions. Elm1 is also a cysteine-rich protein and contains a signal peptide and four domains conserved in the CCN family proteins. Elm1 was highly conserved, expressed ubiquitously in diverse organs, and mapped to mouse chromosome 15. High-metastatic K-1735 M-2 cells, which did not express Elm1, were transfected with an Elm1 expression vector, and several stable clones with Elm1 expression were established. The in vivo growth rates of cells expressing a high level of Elm1 were remarkably slower than those of cells expressing a low level of Elm1. Metastatic potential of transfectants was reduced in proportion to the level of Elm1 expression. Thus, Elm1 is a novel gene of CCN family that can suppress the in vivo growth and metastatic potential of K-1735 mouse melanoma cells.

MeSH Terms
Animals Blotting, Southern CCN Intercellular Signaling Proteins Cell Division/genetics Cloning, Molecular Connective Tissue Growth Factor Cysteine-Rich Protein 61 Gene Expression Regulation, Neoplastic/genetics Genes, Suppressor/genetics Genetic Linkage/genetics Growth Substances/chemistry Immediate-Early Proteins/chemistry Intercellular Signaling Peptides and Proteins Melanoma, Experimental/metabolism Mice Neoplasm Metastasis/genetics Nephroblastoma Overexpressed Protein Oncogene Proteins Oncogene Proteins, Viral/chemistry Proto-Oncogene Proteins/chemistry RNA/analysis Repressor Proteins/chemistry,genetics Sequence Alignment Sequence Analysis, DNA Sequence Homology, Amino Acid Transfection/genetics Tumor Cells, Cultured
Chemicals
CCN Intercellular Signaling Proteins CCN1 protein, mouse CCN2 protein, mouse CCN4 protein, mouse Ccn3 protein, mouse Cysteine-Rich Protein 61 Growth Substances Immediate-Early Proteins Intercellular Signaling Peptides and Proteins Nephroblastoma Overexpressed Protein Oncogene Proteins Oncogene Proteins, Viral Proto-Oncogene Proteins Repressor Proteins Connective Tissue Growth Factor RNA
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Hashimoto Y
Biology Division, National Cancer Center Research Institute, 1-1, Tsukiji 5-chome, Chuo-ku, Tokyo 104, Japan.
Shindo-Okada N
Tani M
Nagamachi Y
Takeuchi K
Shiroishi T
Toma H
Yokota J
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1998-02-02
Pages
289-96
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2212122
Subset
IM
Databases
GENBANK
AB004873
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