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Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.

Unsaturated fatty acids, including n-3 polyunsaturated fatty acids (PUFAs) such as docosahexaenoic acid (C22:6, DHA) and eicosapentaenoic acid (C20:5, EPA), and a series of n-6 PUFAs were investigated for their anti-tumour and antimetastatic effects in a subcutaneous (s.c.) implanted highly metastat...

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Autores principales: Iigo, M., Nakagawa, T., Ishikawa, C., Iwahori, Y., Asamoto, M., Yazawa, K., Araki, E., Tsuda, H.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group|1 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063338/
https://www.ncbi.nlm.nih.gov/pubmed/9043019
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author Iigo, M.
Nakagawa, T.
Ishikawa, C.
Iwahori, Y.
Asamoto, M.
Yazawa, K.
Araki, E.
Tsuda, H.
author_facet Iigo, M.
Nakagawa, T.
Ishikawa, C.
Iwahori, Y.
Asamoto, M.
Yazawa, K.
Araki, E.
Tsuda, H.
author_sort Iigo, M.
collection PubMed
description Unsaturated fatty acids, including n-3 polyunsaturated fatty acids (PUFAs) such as docosahexaenoic acid (C22:6, DHA) and eicosapentaenoic acid (C20:5, EPA), and a series of n-6 PUFAs were investigated for their anti-tumour and antimetastatic effects in a subcutaneous (s.c.) implanted highly metastatic colon carcinoma 26 (Co 26Lu) model. EPA and DHA exerted significant inhibitory effects on tumour growth at the implantation site and significantly decreased the numbers of lung metastatic nodules. Oleic acid also significantly inhibited lung metastatic nodules. Treatment with arachidonic acid showed a tendency for reduction in colonization. However, treatment with high doses of fatty acids, especially linoleic acid, increased the numbers of lung metastatic nodules. DHA and EPA only inhibited lung colonizations when administered together with the tumour cells, suggesting that their incorporation is necessary for an influence to be exerted. Chromatography confirmed that contents of fatty acids in both tumour tissues and plasma were indeed affected by the treatments. Tumour cells pretreated with fatty acids in vivo, in particular DHA, also showed a low potential for lung colony formation when transferred to new hosts. Thus, DHA treatment exerted marked antimetastatic activity associated with pronounced change in the fatty acid component of tumour cells. The results indicate that uptake of DHA into tumour cells results in altered tumour cell membrane characteristics and a decreased ability to metastasize.
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spelling pubmed-20633382009-09-10 Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung. Iigo, M. Nakagawa, T. Ishikawa, C. Iwahori, Y. Asamoto, M. Yazawa, K. Araki, E. Tsuda, H. Br J Cancer Research Article Unsaturated fatty acids, including n-3 polyunsaturated fatty acids (PUFAs) such as docosahexaenoic acid (C22:6, DHA) and eicosapentaenoic acid (C20:5, EPA), and a series of n-6 PUFAs were investigated for their anti-tumour and antimetastatic effects in a subcutaneous (s.c.) implanted highly metastatic colon carcinoma 26 (Co 26Lu) model. EPA and DHA exerted significant inhibitory effects on tumour growth at the implantation site and significantly decreased the numbers of lung metastatic nodules. Oleic acid also significantly inhibited lung metastatic nodules. Treatment with arachidonic acid showed a tendency for reduction in colonization. However, treatment with high doses of fatty acids, especially linoleic acid, increased the numbers of lung metastatic nodules. DHA and EPA only inhibited lung colonizations when administered together with the tumour cells, suggesting that their incorporation is necessary for an influence to be exerted. Chromatography confirmed that contents of fatty acids in both tumour tissues and plasma were indeed affected by the treatments. Tumour cells pretreated with fatty acids in vivo, in particular DHA, also showed a low potential for lung colony formation when transferred to new hosts. Thus, DHA treatment exerted marked antimetastatic activity associated with pronounced change in the fatty acid component of tumour cells. The results indicate that uptake of DHA into tumour cells results in altered tumour cell membrane characteristics and a decreased ability to metastasize. Nature Publishing Group|1 1997 /pmc/articles/PMC2063338/ /pubmed/9043019 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 Research Article
Iigo, M.
Nakagawa, T.
Ishikawa, C.
Iwahori, Y.
Asamoto, M.
Yazawa, K.
Araki, E.
Tsuda, H.
Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.
title Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.
title_full Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.
title_fullStr Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.
title_full_unstemmed Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.
title_short Inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.
title_sort inhibitory effects of docosahexaenoic acid on colon carcinoma 26 metastasis to the lung.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063338/
https://www.ncbi.nlm.nih.gov/pubmed/9043019
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