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Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma Cells
The serum amyloid A (SAA) concentration is higher in mammary tumors with metastases in both humans and animals. In the present study, the direct effects of recombinant feline SAA (rfSAA) protein on invasiveness of feline mammary carcinoma cells were evaluated. As an indicator of invasiveness, matrix...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155205/ https://www.ncbi.nlm.nih.gov/pubmed/24829082 http://dx.doi.org/10.1292/jvms.14-0108 |
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author | TAMAMOTO, Takashi OHNO, Koichi GOTO-KOSHINO, Yuko TSUJIMOTO, Hajime |
author_facet | TAMAMOTO, Takashi OHNO, Koichi GOTO-KOSHINO, Yuko TSUJIMOTO, Hajime |
author_sort | TAMAMOTO, Takashi |
collection | PubMed |
description | The serum amyloid A (SAA) concentration is higher in mammary tumors with metastases in both humans and animals. In the present study, the direct effects of recombinant feline SAA (rfSAA) protein on invasiveness of feline mammary carcinoma cells were evaluated. As an indicator of invasiveness, matrix metalloproteinase-9 (MMP-9) expression was investigated in 4 feline mammary carcinoma cell lines of different origins. In 3 of 4 cell lines, MMP-9 expression was significantly increased by rfSAA stimulation. The invasive capacities of feline mammary carcinoma cells were also stimulated by rfSAA. The findings of this study have identified a novel role for SAA in mammary tumorigenesis and suggest that therapeutic strategies targeting SAA may provide new alternatives in treating tumor invasion and metastasis. |
format | Online Article Text |
id | pubmed-4155205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41552052014-09-05 Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma Cells TAMAMOTO, Takashi OHNO, Koichi GOTO-KOSHINO, Yuko TSUJIMOTO, Hajime J Vet Med Sci Surgery The serum amyloid A (SAA) concentration is higher in mammary tumors with metastases in both humans and animals. In the present study, the direct effects of recombinant feline SAA (rfSAA) protein on invasiveness of feline mammary carcinoma cells were evaluated. As an indicator of invasiveness, matrix metalloproteinase-9 (MMP-9) expression was investigated in 4 feline mammary carcinoma cell lines of different origins. In 3 of 4 cell lines, MMP-9 expression was significantly increased by rfSAA stimulation. The invasive capacities of feline mammary carcinoma cells were also stimulated by rfSAA. The findings of this study have identified a novel role for SAA in mammary tumorigenesis and suggest that therapeutic strategies targeting SAA may provide new alternatives in treating tumor invasion and metastasis. The Japanese Society of Veterinary Science 2014-05-15 2014-08 /pmc/articles/PMC4155205/ /pubmed/24829082 http://dx.doi.org/10.1292/jvms.14-0108 Text en ©2014 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Surgery TAMAMOTO, Takashi OHNO, Koichi GOTO-KOSHINO, Yuko TSUJIMOTO, Hajime Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma Cells |
title | Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma
Cells |
title_full | Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma
Cells |
title_fullStr | Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma
Cells |
title_full_unstemmed | Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma
Cells |
title_short | Serum Amyloid A Promotes Invasion of Feline Mammary Carcinoma
Cells |
title_sort | serum amyloid a promotes invasion of feline mammary carcinoma
cells |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155205/ https://www.ncbi.nlm.nih.gov/pubmed/24829082 http://dx.doi.org/10.1292/jvms.14-0108 |
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