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Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide.

A rat thyroid cancer cell line, FRTC, was established from the normal rat thyroid cell line, FRTL-5. FRTL-5 cells were cultured in vitro with N-acetylmuramyl-L-alanyl-D-isoglutamine (MDP) for 4 days and were transplanted intraperitoneally into Fisher rats. Disseminated tumour formation in the perito...

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Autores principales: Iitaka, M., Fukasawa, N., Kitahama, S., Miura, S., Kawakami, Y., Sato, H., Sugano, S., Ishii, J., Katayama, S.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222688/
https://www.ncbi.nlm.nih.gov/pubmed/9000596
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author Iitaka, M.
Fukasawa, N.
Kitahama, S.
Miura, S.
Kawakami, Y.
Sato, H.
Sugano, S.
Ishii, J.
Katayama, S.
author_facet Iitaka, M.
Fukasawa, N.
Kitahama, S.
Miura, S.
Kawakami, Y.
Sato, H.
Sugano, S.
Ishii, J.
Katayama, S.
author_sort Iitaka, M.
collection PubMed
description A rat thyroid cancer cell line, FRTC, was established from the normal rat thyroid cell line, FRTL-5. FRTL-5 cells were cultured in vitro with N-acetylmuramyl-L-alanyl-D-isoglutamine (MDP) for 4 days and were transplanted intraperitoneally into Fisher rats. Disseminated tumour formation in the peritoneum was found in ten out of ten rats in which MDP-treated FRTL-5 cells were transplanted. Colloid-like structures stained with anti-thyroglobulin (Tg) antibodies were observed in the tumours. On the other hand, no tumour was found in any of the rats in which untreated FRTL-5 cells were transplanted. No morphological changes were observed in FRTL-5 cells after long-term in vitro culture in the presence of MDP. MDP had no effect on thymidine incorporation, the production of cAMP or the expression of c-myc in FRTL-5 cells in vitro. Cells from the tumour (FRTC) secreted Tg in vitro and expressed Tg, thyroid peroxidase (TPO) and thyrotropin (TSH) receptor mRNA. The expression of TSH receptor mRNA increased in FRTC cells after TSH stimulation. FRTC cells produced cAMP in response to TSH stimulation in a dose-dependent manner. However, the growth of FRTC cells was TSH independent. Expression of c-myc and c-fos was observed in FRTC cells in vivo as well as in vitro. FRTC cells formed tumours in Fisher rats when transplanted subcutaneously. FRTC cells have several characteristics of differentiated thyroid cancer cells and may provide a good model for the study of human differentiated thyroid cancers. IMAGES:
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spelling pubmed-22226882009-09-10 Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide. Iitaka, M. Fukasawa, N. Kitahama, S. Miura, S. Kawakami, Y. Sato, H. Sugano, S. Ishii, J. Katayama, S. Br J Cancer Research Article A rat thyroid cancer cell line, FRTC, was established from the normal rat thyroid cell line, FRTL-5. FRTL-5 cells were cultured in vitro with N-acetylmuramyl-L-alanyl-D-isoglutamine (MDP) for 4 days and were transplanted intraperitoneally into Fisher rats. Disseminated tumour formation in the peritoneum was found in ten out of ten rats in which MDP-treated FRTL-5 cells were transplanted. Colloid-like structures stained with anti-thyroglobulin (Tg) antibodies were observed in the tumours. On the other hand, no tumour was found in any of the rats in which untreated FRTL-5 cells were transplanted. No morphological changes were observed in FRTL-5 cells after long-term in vitro culture in the presence of MDP. MDP had no effect on thymidine incorporation, the production of cAMP or the expression of c-myc in FRTL-5 cells in vitro. Cells from the tumour (FRTC) secreted Tg in vitro and expressed Tg, thyroid peroxidase (TPO) and thyrotropin (TSH) receptor mRNA. The expression of TSH receptor mRNA increased in FRTC cells after TSH stimulation. FRTC cells produced cAMP in response to TSH stimulation in a dose-dependent manner. However, the growth of FRTC cells was TSH independent. Expression of c-myc and c-fos was observed in FRTC cells in vivo as well as in vitro. FRTC cells formed tumours in Fisher rats when transplanted subcutaneously. FRTC cells have several characteristics of differentiated thyroid cancer cells and may provide a good model for the study of human differentiated thyroid cancers. IMAGES: Nature Publishing Group 1997 /pmc/articles/PMC2222688/ /pubmed/9000596 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
Iitaka, M.
Fukasawa, N.
Kitahama, S.
Miura, S.
Kawakami, Y.
Sato, H.
Sugano, S.
Ishii, J.
Katayama, S.
Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide.
title Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide.
title_full Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide.
title_fullStr Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide.
title_full_unstemmed Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide.
title_short Transplantable rat thyroid cancer cell line FRTC transformed with muramyl dipeptide.
title_sort transplantable rat thyroid cancer cell line frtc transformed with muramyl dipeptide.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222688/
https://www.ncbi.nlm.nih.gov/pubmed/9000596
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