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Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β

The in vitro invasive capacity of poorly invasive cells (W(1)), which were cloned from rat ascites hepatoma cells (AH 130), was potentiated dose‐ and time‐dependently by pretreating the cells with transforming growth factor‐β (TGF‐β). This potentiation of invasive capacity was completely abolished b...

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Detalles Bibliográficos
Autores principales: Mukai, Mutsuko, Shinkai, Kiyoko, Komatsu, Keiko, Akedo, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917692/
https://www.ncbi.nlm.nih.gov/pubmed/2498244
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02275.x
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author Mukai, Mutsuko
Shinkai, Kiyoko
Komatsu, Keiko
Akedo, Hitoshi
author_facet Mukai, Mutsuko
Shinkai, Kiyoko
Komatsu, Keiko
Akedo, Hitoshi
author_sort Mukai, Mutsuko
collection PubMed
description The in vitro invasive capacity of poorly invasive cells (W(1)), which were cloned from rat ascites hepatoma cells (AH 130), was potentiated dose‐ and time‐dependently by pretreating the cells with transforming growth factor‐β (TGF‐β). This potentiation of invasive capacity was completely abolished by anti‐TGF‐β antibody. When the treated cells were ip inoculated into rats, the cells extensively invaded the peritoneum, and formed penetrating tumor nodules. The effect of TGF‐β was reversed by subculturing the treated cells without TGF‐β. The potentiation of invasive capacity by TGF‐β might participate in platelet‐associated enhancement of tumor cell metastasis.
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spelling pubmed-59176922018-05-11 Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β Mukai, Mutsuko Shinkai, Kiyoko Komatsu, Keiko Akedo, Hitoshi Jpn J Cancer Res Rapid Communication The in vitro invasive capacity of poorly invasive cells (W(1)), which were cloned from rat ascites hepatoma cells (AH 130), was potentiated dose‐ and time‐dependently by pretreating the cells with transforming growth factor‐β (TGF‐β). This potentiation of invasive capacity was completely abolished by anti‐TGF‐β antibody. When the treated cells were ip inoculated into rats, the cells extensively invaded the peritoneum, and formed penetrating tumor nodules. The effect of TGF‐β was reversed by subculturing the treated cells without TGF‐β. The potentiation of invasive capacity by TGF‐β might participate in platelet‐associated enhancement of tumor cell metastasis. Blackwell Publishing Ltd 1989-02 /pmc/articles/PMC5917692/ /pubmed/2498244 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02275.x Text en
spellingShingle Rapid Communication
Mukai, Mutsuko
Shinkai, Kiyoko
Komatsu, Keiko
Akedo, Hitoshi
Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β
title Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β
title_full Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β
title_fullStr Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β
title_full_unstemmed Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β
title_short Potentiation of Invasive Capacity of Rat Ascites Hepatoma Cells by Transforming Growth Factor‐β
title_sort potentiation of invasive capacity of rat ascites hepatoma cells by transforming growth factor‐β
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917692/
https://www.ncbi.nlm.nih.gov/pubmed/2498244
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02275.x
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