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The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells
Pancreatic cancer is one of the most frustrating problems in gastroenterological surgery, since there is little we can do to improve the survival of patients with current treatment strategies. If one is to elucidate factors related to carcinogenesis, tumour biology, diagnostics and new treatment mod...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374401/ https://www.ncbi.nlm.nih.gov/pubmed/10732764 http://dx.doi.org/10.1054/bjoc.1999.1017 |
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author | Mäkinen, K Loimas, S Nuutinen, P Eskelinen, M Alhava, E |
author_facet | Mäkinen, K Loimas, S Nuutinen, P Eskelinen, M Alhava, E |
author_sort | Mäkinen, K |
collection | PubMed |
description | Pancreatic cancer is one of the most frustrating problems in gastroenterological surgery, since there is little we can do to improve the survival of patients with current treatment strategies. If one is to elucidate factors related to carcinogenesis, tumour biology, diagnostics and new treatment modalities of this malignant disease, then it is essential to develop a suitable animal model. In the present study we investigated rat pancreatic tumour growth after intrapancreatic injection of cultured pancreatic carcinoma cells (DSL-6A/C1), originally derived from an azaserine-induced tumour, as well as the features of tumour microcirculation using the microangiography technique. After intrapancreatic inoculation, tumours were detected in 64% of animals. A 1 cm(3)tumour volume was reached within 20 weeks after inoculation. The tumours were ductal adenocarcinomas. Larger tumours showed invasive growth and spreading into the surrounding tissues, mainly into spleen and peritoneum. Microangiography revealed that the pancreatic tumours had an irregular and scanty vessel network and there were avascular areas in the center of the tumour. The area between normal pancreas and the induced tumour had dense vascularization. Intrapancreatic tumour induction with cultured pancreatic carcinoma cells produced a solid and uniformly growing tumour in Lewis rats and it thus provides a possible model for pancreatic cancer studies. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2374401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23744012009-09-10 The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells Mäkinen, K Loimas, S Nuutinen, P Eskelinen, M Alhava, E Br J Cancer Regular Article Pancreatic cancer is one of the most frustrating problems in gastroenterological surgery, since there is little we can do to improve the survival of patients with current treatment strategies. If one is to elucidate factors related to carcinogenesis, tumour biology, diagnostics and new treatment modalities of this malignant disease, then it is essential to develop a suitable animal model. In the present study we investigated rat pancreatic tumour growth after intrapancreatic injection of cultured pancreatic carcinoma cells (DSL-6A/C1), originally derived from an azaserine-induced tumour, as well as the features of tumour microcirculation using the microangiography technique. After intrapancreatic inoculation, tumours were detected in 64% of animals. A 1 cm(3)tumour volume was reached within 20 weeks after inoculation. The tumours were ductal adenocarcinomas. Larger tumours showed invasive growth and spreading into the surrounding tissues, mainly into spleen and peritoneum. Microangiography revealed that the pancreatic tumours had an irregular and scanty vessel network and there were avascular areas in the center of the tumour. The area between normal pancreas and the induced tumour had dense vascularization. Intrapancreatic tumour induction with cultured pancreatic carcinoma cells produced a solid and uniformly growing tumour in Lewis rats and it thus provides a possible model for pancreatic cancer studies. © 2000 Cancer Research Campaign Nature Publishing Group 2000-02 /pmc/articles/PMC2374401/ /pubmed/10732764 http://dx.doi.org/10.1054/bjoc.1999.1017 Text en Copyright © 2000 Cancer Research Campaign 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 | Regular Article Mäkinen, K Loimas, S Nuutinen, P Eskelinen, M Alhava, E The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells |
title | The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells |
title_full | The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells |
title_fullStr | The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells |
title_full_unstemmed | The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells |
title_short | The growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells |
title_sort | growth pattern and microvasculature of pancreatic tumours induced with cultured carcinoma cells |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374401/ https://www.ncbi.nlm.nih.gov/pubmed/10732764 http://dx.doi.org/10.1054/bjoc.1999.1017 |
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