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Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis

Two non‐tumorigenic variant cells were isolated from UV‐irradiated Balb/c 3T3 cells on the basis of their different responsiveness in phorbol ester‐induced morphological change (rounding formation). They showed marked differences of lung metastatic potentials after intravenous injections of their v‐...

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Detalles Bibliográficos
Autores principales: Enomoto, Taira, Ayaki, Hitoshi, Nakamori, Shoji, Enomoto, Yuko, Inoue, Hirokazu, Kakunaga, Takeo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918072/
https://www.ncbi.nlm.nih.gov/pubmed/2116399
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02598.x
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author Enomoto, Taira
Ayaki, Hitoshi
Nakamori, Shoji
Enomoto, Yuko
Inoue, Hirokazu
Kakunaga, Takeo
author_facet Enomoto, Taira
Ayaki, Hitoshi
Nakamori, Shoji
Enomoto, Yuko
Inoue, Hirokazu
Kakunaga, Takeo
author_sort Enomoto, Taira
collection PubMed
description Two non‐tumorigenic variant cells were isolated from UV‐irradiated Balb/c 3T3 cells on the basis of their different responsiveness in phorbol ester‐induced morphological change (rounding formation). They showed marked differences of lung metastatic potentials after intravenous injections of their v‐src transformants into nude mice; phorbol ester‐resistant variant TR4 cells transformed by v‐src were hypermetastatic, whereas v‐src transformants of phorbol ester‐sensitive variant TR5 cells were not metastatic at all. These different metastatic responses were not observed in v‐K‐ras‐induced transformants of the variants. These non‐tumorigenic variant cells may pre‐acquire the genetic alteration of certain src‐specific and metastasis‐associated factors. This system may be useful for genetic analysis of the induction of metastasis.
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spelling pubmed-59180722018-05-11 Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis Enomoto, Taira Ayaki, Hitoshi Nakamori, Shoji Enomoto, Yuko Inoue, Hirokazu Kakunaga, Takeo Jpn J Cancer Res Article Two non‐tumorigenic variant cells were isolated from UV‐irradiated Balb/c 3T3 cells on the basis of their different responsiveness in phorbol ester‐induced morphological change (rounding formation). They showed marked differences of lung metastatic potentials after intravenous injections of their v‐src transformants into nude mice; phorbol ester‐resistant variant TR4 cells transformed by v‐src were hypermetastatic, whereas v‐src transformants of phorbol ester‐sensitive variant TR5 cells were not metastatic at all. These different metastatic responses were not observed in v‐K‐ras‐induced transformants of the variants. These non‐tumorigenic variant cells may pre‐acquire the genetic alteration of certain src‐specific and metastasis‐associated factors. This system may be useful for genetic analysis of the induction of metastasis. Blackwell Publishing Ltd 1990-05 /pmc/articles/PMC5918072/ /pubmed/2116399 http://dx.doi.org/10.1111/j.1349-7006.1990.tb02598.x Text en
spellingShingle Article
Enomoto, Taira
Ayaki, Hitoshi
Nakamori, Shoji
Enomoto, Yuko
Inoue, Hirokazu
Kakunaga, Takeo
Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis
title Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis
title_full Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis
title_fullStr Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis
title_full_unstemmed Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis
title_short Novel Non‐tumorigenic Cell Variants Showing Potentially Different Susceptibility to v‐src‐induced Metastasis
title_sort novel non‐tumorigenic cell variants showing potentially different susceptibility to v‐src‐induced metastasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918072/
https://www.ncbi.nlm.nih.gov/pubmed/2116399
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02598.x
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