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Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor

The inhibitory effect of the protease inhibitor aprotinin (Trasylol) on the invasion of mouse kidney explants by polyoma virus transformed BHK21 cells was investigated using a mixed cell/organ culture technique. The extent of invasion was monitored by following the changes in LDH isoenzyme pattern i...

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Detalles Bibliográficos
Autores principales: Latner, A. L., Longstaff, E., Pradhan, K.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1973
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008808/
https://www.ncbi.nlm.nih.gov/pubmed/4352791
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author Latner, A. L.
Longstaff, E.
Pradhan, K.
author_facet Latner, A. L.
Longstaff, E.
Pradhan, K.
author_sort Latner, A. L.
collection PubMed
description The inhibitory effect of the protease inhibitor aprotinin (Trasylol) on the invasion of mouse kidney explants by polyoma virus transformed BHK21 cells was investigated using a mixed cell/organ culture technique. The extent of invasion was monitored by following the changes in LDH isoenzyme pattern in the explants and by histological assessment. The kidney explants containing aprotinin were found to maintain a normal kidney LDH pattern and to suffer considerably less invasion than the explants not containing the drug. These results support the idea that proteolytic enzymes are associated with invasion and that inhibitors of protease activity could possibly be useful in the management of clinical cancer.
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spelling pubmed-20088082009-09-10 Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor Latner, A. L. Longstaff, E. Pradhan, K. Br J Cancer Articles The inhibitory effect of the protease inhibitor aprotinin (Trasylol) on the invasion of mouse kidney explants by polyoma virus transformed BHK21 cells was investigated using a mixed cell/organ culture technique. The extent of invasion was monitored by following the changes in LDH isoenzyme pattern in the explants and by histological assessment. The kidney explants containing aprotinin were found to maintain a normal kidney LDH pattern and to suffer considerably less invasion than the explants not containing the drug. These results support the idea that proteolytic enzymes are associated with invasion and that inhibitors of protease activity could possibly be useful in the management of clinical cancer. Nature Publishing Group 1973-06 /pmc/articles/PMC2008808/ /pubmed/4352791 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Articles
Latner, A. L.
Longstaff, E.
Pradhan, K.
Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor
title Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor
title_full Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor
title_fullStr Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor
title_full_unstemmed Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor
title_short Inhibition of Malignant Cell Invasion in vitro by a Proteinase Inhibitor
title_sort inhibition of malignant cell invasion in vitro by a proteinase inhibitor
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008808/
https://www.ncbi.nlm.nih.gov/pubmed/4352791
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