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Impact of fibroblast activation protein on osteosarcoma cell lines in vitro

Fibroblast activation protein (FAP) or seprase, which belongs to the group type II integral serine proteases, is an integral membrane serine peptidase. Previous studies have demonstrated that FAP has an effect on tumor growth, proliferation and invasion. However, the cellular functional role that FA...

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Autores principales: DING, LIXIANG, YE, LIN, XU, JIANLI, JIANG, WEN G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919928/
https://www.ncbi.nlm.nih.gov/pubmed/24520291
http://dx.doi.org/10.3892/ol.2014.1788
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author DING, LIXIANG
YE, LIN
XU, JIANLI
JIANG, WEN G.
author_facet DING, LIXIANG
YE, LIN
XU, JIANLI
JIANG, WEN G.
author_sort DING, LIXIANG
collection PubMed
description Fibroblast activation protein (FAP) or seprase, which belongs to the group type II integral serine proteases, is an integral membrane serine peptidase. Previous studies have demonstrated that FAP has an effect on tumor growth, proliferation and invasion. However, the cellular functional role that FAP plays in osteosarcoma (OS) remains unknown. The aim of the present study was to investigate the activities of FAP in OS cell lines. The gene expression of FAP was knocked down through a hammerhead ribozyme transgene, and the various functions between the knockdown cells and their control cells were tested using a series of functional assays in vitro. The results indicated that knockdown of FAP markedly reduced the ability of cellular growth, matrix adhesion, migration and invasion in MG-63 and HOS cell lines compared with the control cells (P<0.05). In conclusion, FAP influences OS cells and may play a role in OS tumor progression and metastasis.
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spelling pubmed-39199282014-02-11 Impact of fibroblast activation protein on osteosarcoma cell lines in vitro DING, LIXIANG YE, LIN XU, JIANLI JIANG, WEN G. Oncol Lett Articles Fibroblast activation protein (FAP) or seprase, which belongs to the group type II integral serine proteases, is an integral membrane serine peptidase. Previous studies have demonstrated that FAP has an effect on tumor growth, proliferation and invasion. However, the cellular functional role that FAP plays in osteosarcoma (OS) remains unknown. The aim of the present study was to investigate the activities of FAP in OS cell lines. The gene expression of FAP was knocked down through a hammerhead ribozyme transgene, and the various functions between the knockdown cells and their control cells were tested using a series of functional assays in vitro. The results indicated that knockdown of FAP markedly reduced the ability of cellular growth, matrix adhesion, migration and invasion in MG-63 and HOS cell lines compared with the control cells (P<0.05). In conclusion, FAP influences OS cells and may play a role in OS tumor progression and metastasis. D.A. Spandidos 2014-03 2014-01-10 /pmc/articles/PMC3919928/ /pubmed/24520291 http://dx.doi.org/10.3892/ol.2014.1788 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
DING, LIXIANG
YE, LIN
XU, JIANLI
JIANG, WEN G.
Impact of fibroblast activation protein on osteosarcoma cell lines in vitro
title Impact of fibroblast activation protein on osteosarcoma cell lines in vitro
title_full Impact of fibroblast activation protein on osteosarcoma cell lines in vitro
title_fullStr Impact of fibroblast activation protein on osteosarcoma cell lines in vitro
title_full_unstemmed Impact of fibroblast activation protein on osteosarcoma cell lines in vitro
title_short Impact of fibroblast activation protein on osteosarcoma cell lines in vitro
title_sort impact of fibroblast activation protein on osteosarcoma cell lines in vitro
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919928/
https://www.ncbi.nlm.nih.gov/pubmed/24520291
http://dx.doi.org/10.3892/ol.2014.1788
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