Cargando…
Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats
To investigate the differences between the effects of mesenchymal stem cells (MSCs) administered in the early and late phases of tumorigenesis, MSCs were isolated from bone marrow and colorectal tumors were produced by exposing 7-week-old F344 rats to 1,2-dimethylhydrazine and dextran sulfate sodium...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818273/ https://www.ncbi.nlm.nih.gov/pubmed/24249972 http://dx.doi.org/10.3164/jcbn.13-68 |
_version_ | 1782478166789455872 |
---|---|
author | Katsuno, Takayuki Ochi, Masahiro Tominaga, Kazunari Tanaka, Fumio Sogawa, Mitsue Tanigawa, Tetsuya Yamagami, Hirokazu Shiba, Masatsugu Watanabe, Kenji Watanabe, Toshio Fujiwara, Yasuhiro Arakawa, Tetsuo |
author_facet | Katsuno, Takayuki Ochi, Masahiro Tominaga, Kazunari Tanaka, Fumio Sogawa, Mitsue Tanigawa, Tetsuya Yamagami, Hirokazu Shiba, Masatsugu Watanabe, Kenji Watanabe, Toshio Fujiwara, Yasuhiro Arakawa, Tetsuo |
author_sort | Katsuno, Takayuki |
collection | PubMed |
description | To investigate the differences between the effects of mesenchymal stem cells (MSCs) administered in the early and late phases of tumorigenesis, MSCs were isolated from bone marrow and colorectal tumors were produced by exposing 7-week-old F344 rats to 1,2-dimethylhydrazine and dextran sulfate sodium. We evaluated tumor number and volume (week 25), MSC localization, number of aberrant crypt foci (ACF), transforming growth factor (TGF)-β1 protein levels in the rectum after administration of MSCs (week 5 or 15), and the effects of MSC-conditioned medium on ACL15 cell proliferation. Administered MSCs labeled with PKH26 were observed in the rectum. Administered MSCs in the early phase (week 5) before tumor occurrence (week 12) significantly decreased tumor number and volume (1.5 vs 4 and 21 mm(3) vs 170 mm(3); p<0.01), but not administered MSCs in the late phase (week 15). Administered MSCs in the early phase reduced ACF number on days 14 and 35 (1.9 vs 4.1 and 3.7 vs 7.3; p<0.01). Rectal TGF-β1 increased 1.3 fold on day 3, and MSC-conditioned medium containing TGF-β1 abundantly inhibited ACL15 cell proliferation. MSCs administered in the early phase but not late phase inhibited colorectal tumor development in a rat model. |
format | Online Article Text |
id | pubmed-3818273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-38182732013-11-18 Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats Katsuno, Takayuki Ochi, Masahiro Tominaga, Kazunari Tanaka, Fumio Sogawa, Mitsue Tanigawa, Tetsuya Yamagami, Hirokazu Shiba, Masatsugu Watanabe, Kenji Watanabe, Toshio Fujiwara, Yasuhiro Arakawa, Tetsuo J Clin Biochem Nutr Original Article To investigate the differences between the effects of mesenchymal stem cells (MSCs) administered in the early and late phases of tumorigenesis, MSCs were isolated from bone marrow and colorectal tumors were produced by exposing 7-week-old F344 rats to 1,2-dimethylhydrazine and dextran sulfate sodium. We evaluated tumor number and volume (week 25), MSC localization, number of aberrant crypt foci (ACF), transforming growth factor (TGF)-β1 protein levels in the rectum after administration of MSCs (week 5 or 15), and the effects of MSC-conditioned medium on ACL15 cell proliferation. Administered MSCs labeled with PKH26 were observed in the rectum. Administered MSCs in the early phase (week 5) before tumor occurrence (week 12) significantly decreased tumor number and volume (1.5 vs 4 and 21 mm(3) vs 170 mm(3); p<0.01), but not administered MSCs in the late phase (week 15). Administered MSCs in the early phase reduced ACF number on days 14 and 35 (1.9 vs 4.1 and 3.7 vs 7.3; p<0.01). Rectal TGF-β1 increased 1.3 fold on day 3, and MSC-conditioned medium containing TGF-β1 abundantly inhibited ACL15 cell proliferation. MSCs administered in the early phase but not late phase inhibited colorectal tumor development in a rat model. the Society for Free Radical Research Japan 2013-11 2013-10-31 /pmc/articles/PMC3818273/ /pubmed/24249972 http://dx.doi.org/10.3164/jcbn.13-68 Text en Copyright © 2013 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Katsuno, Takayuki Ochi, Masahiro Tominaga, Kazunari Tanaka, Fumio Sogawa, Mitsue Tanigawa, Tetsuya Yamagami, Hirokazu Shiba, Masatsugu Watanabe, Kenji Watanabe, Toshio Fujiwara, Yasuhiro Arakawa, Tetsuo Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats |
title | Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats |
title_full | Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats |
title_fullStr | Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats |
title_full_unstemmed | Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats |
title_short | Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats |
title_sort | mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818273/ https://www.ncbi.nlm.nih.gov/pubmed/24249972 http://dx.doi.org/10.3164/jcbn.13-68 |
work_keys_str_mv | AT katsunotakayuki mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT ochimasahiro mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT tominagakazunari mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT tanakafumio mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT sogawamitsue mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT tanigawatetsuya mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT yamagamihirokazu mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT shibamasatsugu mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT watanabekenji mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT watanabetoshio mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT fujiwarayasuhiro mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats AT arakawatetsuo mesenchymalstemcellsadministeredintheearlyphaseoftumorigenesisinhibitcolorectaltumordevelopmentinrats |