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Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).

The QR regressor tumour (QR-32), a fibrosarcoma which is unable to grow progressively in normal syngeneic C57BL/6 mice, was able to grow progressively in 13 out of 22 mice (59%) when it was subcutaneously coimplanted with gelatin sponge. We established four culture tumour lines from the resultant tu...

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Autores principales: Okada, F., Hosokawa, M., Hamada, J. I., Hasegawa, J., Kato, M., Mizutani, M., Ren, J., Takeichi, N., Kobayashi, H.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977431/
https://www.ncbi.nlm.nih.gov/pubmed/1419599
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author Okada, F.
Hosokawa, M.
Hamada, J. I.
Hasegawa, J.
Kato, M.
Mizutani, M.
Ren, J.
Takeichi, N.
Kobayashi, H.
author_facet Okada, F.
Hosokawa, M.
Hamada, J. I.
Hasegawa, J.
Kato, M.
Mizutani, M.
Ren, J.
Takeichi, N.
Kobayashi, H.
author_sort Okada, F.
collection PubMed
description The QR regressor tumour (QR-32), a fibrosarcoma which is unable to grow progressively in normal syngeneic C57BL/6 mice, was able to grow progressively in 13 out of 22 mice (59%) when it was subcutaneously coimplanted with gelatin sponge. We established four culture tumour lines from the resultant tumours (QRsP tumour lines). These QRsP tumour lines were able to grow progressively in mice even in the absence of gelatin sponge. The ability of QRsP tumour cells to colonise the lungs after intravenous injection and to produce high amounts of prostaglandin E2 (PGE2) during in vitro cell culture was much greater than that of parent QR-32 cells. These biological characteristics of QR-32 cells and QRsP tumour cells were found to be stable for at least 6 months when they were maintained in culture. We also observed that QR-32 cells were able to grow progressively in five out of 12 (42%) mice after coimplantation with plastic non-adherent peritoneal cells obtained from mice which had been intraperitoneally implanted with gelatin sponge. These host cells reactive to gelatin sponge increased the production of high amounts of PGE2 by QR-32 cells during 48 h coculture. Preliminary in vitro studies implicated the involvement of hydrogen peroxide and hydroxyl radical as some of the factors necessary to induce QR-32 cells to produce high amounts of PGE2 and to accelerate tumour progression.
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spelling pubmed-19774312009-09-10 Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge). Okada, F. Hosokawa, M. Hamada, J. I. Hasegawa, J. Kato, M. Mizutani, M. Ren, J. Takeichi, N. Kobayashi, H. Br J Cancer Research Article The QR regressor tumour (QR-32), a fibrosarcoma which is unable to grow progressively in normal syngeneic C57BL/6 mice, was able to grow progressively in 13 out of 22 mice (59%) when it was subcutaneously coimplanted with gelatin sponge. We established four culture tumour lines from the resultant tumours (QRsP tumour lines). These QRsP tumour lines were able to grow progressively in mice even in the absence of gelatin sponge. The ability of QRsP tumour cells to colonise the lungs after intravenous injection and to produce high amounts of prostaglandin E2 (PGE2) during in vitro cell culture was much greater than that of parent QR-32 cells. These biological characteristics of QR-32 cells and QRsP tumour cells were found to be stable for at least 6 months when they were maintained in culture. We also observed that QR-32 cells were able to grow progressively in five out of 12 (42%) mice after coimplantation with plastic non-adherent peritoneal cells obtained from mice which had been intraperitoneally implanted with gelatin sponge. These host cells reactive to gelatin sponge increased the production of high amounts of PGE2 by QR-32 cells during 48 h coculture. Preliminary in vitro studies implicated the involvement of hydrogen peroxide and hydroxyl radical as some of the factors necessary to induce QR-32 cells to produce high amounts of PGE2 and to accelerate tumour progression. Nature Publishing Group 1992-10 /pmc/articles/PMC1977431/ /pubmed/1419599 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
Okada, F.
Hosokawa, M.
Hamada, J. I.
Hasegawa, J.
Kato, M.
Mizutani, M.
Ren, J.
Takeichi, N.
Kobayashi, H.
Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).
title Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).
title_full Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).
title_fullStr Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).
title_full_unstemmed Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).
title_short Malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).
title_sort malignant progression of a mouse fibrosarcoma by host cells reactive to a foreign body (gelatin sponge).
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977431/
https://www.ncbi.nlm.nih.gov/pubmed/1419599
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