Identification of an amino acid sequence from the laminin A chain that stimulates metastasis and collagenase IV production

T. Kanemoto, R. Reich, L. Royce, D. Greatorex, S. H. Adler, N. Shiraishi, G. R. Martin, Y. Yamada, H. K. Kleinman*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

177 Scopus citations

Abstract

Tumor cells attach, degrade, and migrate through basement membranes as they metastasize. Laminin, a major glycoprotein of basement membranes, promotes the metastatic activity of tumor cells by stimulating the attachment and migration of the cells and their secretion of collagenase IV. We have identified a synthetic peptide of 19 amino acids (Cys-Ser-Arg-Ala-Arg-Lys-Gln-Ala-Ala-Ser-Ile-Lys-Val-Ala-Val-Ser-Ala-Asp-Arg) from the sequence of the A chain of laminin that increases experimental metastases of the lungs by murine melanoma cells. The peptide is active when injected either intravenously or intraperitoneally. The peptide increased collagenase IV activity, a key enzyme in the breakdown of basement membranes, to the same extent as laminin. This peptide represents an active site on laminin for promotion of the metastatic phenotype and generates a probe for studying the regulation of malignant activities.

Original languageEnglish
Pages (from-to)2279-2283
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume87
Issue number6
StatePublished - Mar 1990
Externally publishedYes

Keywords

  • Basement membrane
  • Extracellular matrix
  • Protease
  • Tumor

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