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Involvement of hyaluronidases in colorectal cancer
BACKGROUND: Hyaluronidases belong to a class of enzymes that degrade, predominantly, hyaluronan. These enzymes are known to be involved in physiological and pathological processes, such as tumor growth, infiltration and angiogenesis, but their exact role in tumor promotion or suppression is not clea...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949809/ https://www.ncbi.nlm.nih.gov/pubmed/20849597 http://dx.doi.org/10.1186/1471-2407-10-499 |
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author | Bouga, Helen Tsouros, Isidoros Bounias, Dimitrios Kyriakopoulou, Dora Stavropoulos, Michael S Papageorgakopoulou, Nikoletta Theocharis, Dimitrios A Vynios, Demitrios H |
author_facet | Bouga, Helen Tsouros, Isidoros Bounias, Dimitrios Kyriakopoulou, Dora Stavropoulos, Michael S Papageorgakopoulou, Nikoletta Theocharis, Dimitrios A Vynios, Demitrios H |
author_sort | Bouga, Helen |
collection | PubMed |
description | BACKGROUND: Hyaluronidases belong to a class of enzymes that degrade, predominantly, hyaluronan. These enzymes are known to be involved in physiological and pathological processes, such as tumor growth, infiltration and angiogenesis, but their exact role in tumor promotion or suppression is not clear yet. Advanced colorectal cancer is associated with elevated amounts of hyaluronan of varying size. The aim of the present study was therefore to illuminate the importance of hyaluronidases in colon carcinoma progression. METHODS: The patients' samples (macroscopically normal and cancerous) were subjected to sequential extraction with PBS, 4 M GdnHCl and 4 M GdnHCl - 1% Triton X-100. The presence of the various hyaluronidases in the extracts was examined by zymography and western blotting. Their expression was also examined by RT-PCR. RESULTS: Among hyaluronidases examined, Hyal-1, -2, -3 and PH-20 were detected. Their activity was higher in cancerous samples. Hyal-1 and Hyal-2 were overexpressed in cancerous samples, especially in advanced stages of cancer. Both isoforms were mainly extracted with PBS. Hyal-3 was observed only in the third extract of advanced stages of cancer. PH-20 was abundant in all three extracts of all stages of cancer. The expression of only Hyal-1 and PH-20 was verified by RT-PCR. CONCLUSION: A high association of hyaluronidases in colorectal cancer was observed. Each hyaluronidase presented different tissue distribution, which indicated the implication of certain isoforms in certain cancer stages. The results provided new evidence on the mechanisms involved in the progression of colorectal cancer. |
format | Text |
id | pubmed-2949809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29498092010-10-06 Involvement of hyaluronidases in colorectal cancer Bouga, Helen Tsouros, Isidoros Bounias, Dimitrios Kyriakopoulou, Dora Stavropoulos, Michael S Papageorgakopoulou, Nikoletta Theocharis, Dimitrios A Vynios, Demitrios H BMC Cancer Research Article BACKGROUND: Hyaluronidases belong to a class of enzymes that degrade, predominantly, hyaluronan. These enzymes are known to be involved in physiological and pathological processes, such as tumor growth, infiltration and angiogenesis, but their exact role in tumor promotion or suppression is not clear yet. Advanced colorectal cancer is associated with elevated amounts of hyaluronan of varying size. The aim of the present study was therefore to illuminate the importance of hyaluronidases in colon carcinoma progression. METHODS: The patients' samples (macroscopically normal and cancerous) were subjected to sequential extraction with PBS, 4 M GdnHCl and 4 M GdnHCl - 1% Triton X-100. The presence of the various hyaluronidases in the extracts was examined by zymography and western blotting. Their expression was also examined by RT-PCR. RESULTS: Among hyaluronidases examined, Hyal-1, -2, -3 and PH-20 were detected. Their activity was higher in cancerous samples. Hyal-1 and Hyal-2 were overexpressed in cancerous samples, especially in advanced stages of cancer. Both isoforms were mainly extracted with PBS. Hyal-3 was observed only in the third extract of advanced stages of cancer. PH-20 was abundant in all three extracts of all stages of cancer. The expression of only Hyal-1 and PH-20 was verified by RT-PCR. CONCLUSION: A high association of hyaluronidases in colorectal cancer was observed. Each hyaluronidase presented different tissue distribution, which indicated the implication of certain isoforms in certain cancer stages. The results provided new evidence on the mechanisms involved in the progression of colorectal cancer. BioMed Central 2010-09-17 /pmc/articles/PMC2949809/ /pubmed/20849597 http://dx.doi.org/10.1186/1471-2407-10-499 Text en Copyright ©2010 Bouga et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bouga, Helen Tsouros, Isidoros Bounias, Dimitrios Kyriakopoulou, Dora Stavropoulos, Michael S Papageorgakopoulou, Nikoletta Theocharis, Dimitrios A Vynios, Demitrios H Involvement of hyaluronidases in colorectal cancer |
title | Involvement of hyaluronidases in colorectal cancer |
title_full | Involvement of hyaluronidases in colorectal cancer |
title_fullStr | Involvement of hyaluronidases in colorectal cancer |
title_full_unstemmed | Involvement of hyaluronidases in colorectal cancer |
title_short | Involvement of hyaluronidases in colorectal cancer |
title_sort | involvement of hyaluronidases in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949809/ https://www.ncbi.nlm.nih.gov/pubmed/20849597 http://dx.doi.org/10.1186/1471-2407-10-499 |
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