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PMID: 1801721 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The malignant phenotype and cysteine proteinases.

Biomedica biochimica acta ·Vol. 50 ·No. 4-6 ·1991-00-00 ·Pages 549-54

Sloane BF, Rozhin J, Krepela E, Ziegler G, Sameni M

Abstract

Expression, membrane association and secretion of both cathepsin B and cathepsin L have been associated with the malignant phenotype of murine B16 melanomas. Only native forms of the two enzymes were found in the lysosomal fractions, whereas both native and latent forms were found in the membrane fractions. Brief exposure to acid pH induced secretion of only native forms of both cathepsin B and cathepsin L and a concomitant reduction in membrane-associated activities. Thus, the pericellular acidification associated with malignant tumors may provide optimal conditions for proteolysis by the cysteine proteinases in terms of their enhanced stability and their induced release in native forms not requiring proteolytic activation.

MeSH Terms
Animals Cathepsin B/metabolism Cathepsin L Cathepsins/metabolism Cell Membrane/enzymology Cysteine Endopeptidases Endopeptidases Hydrogen-Ion Concentration Lysosomes/enzymology Melanoma, Experimental/enzymology Phenotype Tumor Cells, Cultured/enzymology
Chemicals
Cathepsins Endopeptidases Cysteine Endopeptidases Cathepsin B Cathepsin L
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sloane B F
Department of Pharmacology, Wayne State University, Detroit, Michigan 48201.
Rozhin J
Krepela E
Ziegler G
Sameni M
Article Info
Journal
Biomedica biochimica acta
Abbr.
Biomed Biochim Acta
ISSN
0232-766X
Published
1991-00-00
Pages
549-54
Language
English
Region
Germany
NLM ID
8304435
Subset
IM
Grants
NCI NIH HHS · CA 36481 · United States
NCI NIH HHS · CA 48210 · United States
External Links
PubMed source
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