Startseite Effect of Cysteine Proteinase Inhibitors on Murine B16 Melanoma Cell Invasion in vitro
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Effect of Cysteine Proteinase Inhibitors on Murine B16 Melanoma Cell Invasion in vitro

  • Natasa Sever , Metka Filipic , Joze Brzin und Tamara T. Lah
Veröffentlicht/Copyright: 1. Juni 2005
Biological Chemistry
Aus der Zeitschrift Band 383 Heft 5

Abstract

Various types of proteinases are implicated in the malignant progression of human and animal tumors. Proteinase inhibitors may therefore be useful as therapeutic agents in antiinvasive and antimetastatic treatment. The aims of this study were (1) to estimate the relative importance of proteinases in B16 cell invasion in vitro using synthetic, classspecific proteinase inhibitors and (2) to assess the inhibitory effect of some naturally occurring cysteine proteinase inhibitors. Serine proteinase inhibitor reduced invasiveness by up to 24%, whereas inhibition of aspartic proteinases reduced invasion by 11%. Synthetic inhibitors of cysteine proteinases markedly impaired invasion: cathepsin B inhibitors, particularly Ca 074Me, inhibited invasion from 20 40%, whereas cathepsin L inhibitor Clik 148 reduced invasion by 11%. The potato cysteine proteinase inhibitor PCPI 8.7 inhibited invasion by 21%, whereas another potato inhibitor, PCPI 6.6, and the mushroom cysteine proteinase inhibitor clitocypin had no effects. As the inhibitors that inhibited cathepsin B were in general more efficient at impairing the invasiveness, we conclude that of the two cysteine proteinases, cathepsin B plays a more important role than cathepsin L in murine melanoma cell invasion.

:
Published Online: 2005-06-01
Published in Print: 2002-05-15

Copyright © 2002 by Walter de Gruyter GmbH & Co. KG

Artikel in diesem Heft

  1. Nobuhiko Katunuma: An Outstanding Scientific and Professional Career of a Warm-Hearted Person. Reflections on the Occasion of his 75th Birthday
  2. Structural and Functional Diversity of Connexin Genes in the Mouse and Human Genome
  3. Congopain from Trypanosoma congolense: Drug Target and Vaccine Candidate
  4. Biosynthesis of Lysosomal Proteinases in Health and Disease
  5. Calpain Function in the Differentiation of Mesenchymal Stem Cells
  6. Ku Antigen Supports Termination of Mammalian rDNA Replication by Transcription Termination Factor TTF-I
  7. Thyroid Stimulating Hormone Upregulates Secretion of Cathepsin B from Thyroid Epithelial Cells
  8. Selective Release of Calpain Produced αII-Spectrin (α-Fodrin) Breakdown Products by Acute Neuronal Cell Death
  9. Altered Storage of Proteases in Mast Cells from Mice Lacking Heparin: A Possible Role for Heparin Carboxypeptidase A Processing
  10. Clustering-Induced Signaling of CEACAM1 in PC12 Cells
  11. Spin Adducts of Superoxide, Alkoxyl, and Lipid-Derived Radicals with EMPO and Its Derivatives
  12. Glutathione S-Transferase of the Malarial Parasite Plasmodium falciparum: Characterization of a Potential Drug Target
  13. Analysis of the Structural Determinants for RNA Binding of the Human Protein AUF1/hnRNP D
  14. Effect of Cysteine Proteinase Inhibitors on Murine B16 Melanoma Cell Invasion in vitro
  15. Stage-Specific Antimalarial Activity of Cysteine Protease Inhibitors
  16. Epoxysuccinyl Peptide-Derived Cathepsin B Inhibitors: Modulating Membrane Permeability by Conjugation with the C-Terminal Heptapeptide Segment of Penetratin
  17. Design of Inhibitors for Human Tissue Kallikrein Using Non-Natural Aromatic and Basic Amino Acids
  18. Amyloid Fibril Formation by Human Stefin B in vitro: Immunogold Labelling and Comparison to Stefin A
  19. Lysosomal Peptidases and Glycosidases in Rheumatoid Arthritis
Heruntergeladen am 7.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/BC.2002.088/html
Button zum nach oben scrollen