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Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties.
Freshly isolated cones of high cloning efficiency from a mouse fibrosarcoma were examined for DNA content, cell size, protein content, and malignant characteristics such as artificial lung-colony-forming ability, s.c. tumour take, host survival, and spontaneous metastatic ability. These malignant ch...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1980
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010545/ https://www.ncbi.nlm.nih.gov/pubmed/7459211 |
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author | Suzuki, N. Williams, M. Hunter, N. M. Withers, H. R. |
author_facet | Suzuki, N. Williams, M. Hunter, N. M. Withers, H. R. |
author_sort | Suzuki, N. |
collection | PubMed |
description | Freshly isolated cones of high cloning efficiency from a mouse fibrosarcoma were examined for DNA content, cell size, protein content, and malignant characteristics such as artificial lung-colony-forming ability, s.c. tumour take, host survival, and spontaneous metastatic ability. These malignant characteristics and other cell properties were heterogeneous among these clones; the malignant characteristics could vary and were not "all or none" in their nature. The higher the DNA content or the larger the cell volume, the higher the malignancy in terms of artificial lung-colony forming, efficiency, s.c. tumour take, and host survival. Despite variability of each parameter, the ratio of DNA content to cell size or protein content remained constant through these variations: the increased DNA paralleled increased protein and increased cell volume. The increased DNA was correlated with the more malignant characteristics of local growth and lung-colony-forming efficiency. Spontaneous metastasis to the lung was totally different from the local growth abilities; the small-cell clone produced more metastases. The graded nature of malignant properties and the differentiation between local growth and metastatic potential among the daughter clones indicate that malignancy reflects a complex moiety of cell properties. |
format | Text |
id | pubmed-2010545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1980 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20105452009-09-10 Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. Suzuki, N. Williams, M. Hunter, N. M. Withers, H. R. Br J Cancer Research Article Freshly isolated cones of high cloning efficiency from a mouse fibrosarcoma were examined for DNA content, cell size, protein content, and malignant characteristics such as artificial lung-colony-forming ability, s.c. tumour take, host survival, and spontaneous metastatic ability. These malignant characteristics and other cell properties were heterogeneous among these clones; the malignant characteristics could vary and were not "all or none" in their nature. The higher the DNA content or the larger the cell volume, the higher the malignancy in terms of artificial lung-colony forming, efficiency, s.c. tumour take, and host survival. Despite variability of each parameter, the ratio of DNA content to cell size or protein content remained constant through these variations: the increased DNA paralleled increased protein and increased cell volume. The increased DNA was correlated with the more malignant characteristics of local growth and lung-colony-forming efficiency. Spontaneous metastasis to the lung was totally different from the local growth abilities; the small-cell clone produced more metastases. The graded nature of malignant properties and the differentiation between local growth and metastatic potential among the daughter clones indicate that malignancy reflects a complex moiety of cell properties. Nature Publishing Group 1980-11 /pmc/articles/PMC2010545/ /pubmed/7459211 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 Suzuki, N. Williams, M. Hunter, N. M. Withers, H. R. Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. |
title | Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. |
title_full | Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. |
title_fullStr | Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. |
title_full_unstemmed | Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. |
title_short | Malignant properties and DNA content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. |
title_sort | malignant properties and dna content of daughter clones from a mouse fibrosarcoma: differentiation between malignant properties. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010545/ https://www.ncbi.nlm.nih.gov/pubmed/7459211 |
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