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Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin

The Sleeping Beauty transposon system is used as a tool for insertional mutagenesis and oncogenesis. However, little is known about the exact histological phenotype of the tumors induced. Thus, we used immunohistochemical markers to enable histological identification of the type of tumor induced by...

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Detalles Bibliográficos
Autores principales: JUNG, SUNYOUNG, RO, SIMON WEONSANG, JUNG, GEUNYOUNG, JU, HYE-LIM, YU, EUN-SIL, SON, WOO-CHAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621733/
https://www.ncbi.nlm.nih.gov/pubmed/23380875
http://dx.doi.org/10.3892/or.2013.2264
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author JUNG, SUNYOUNG
RO, SIMON WEONSANG
JUNG, GEUNYOUNG
JU, HYE-LIM
YU, EUN-SIL
SON, WOO-CHAN
author_facet JUNG, SUNYOUNG
RO, SIMON WEONSANG
JUNG, GEUNYOUNG
JU, HYE-LIM
YU, EUN-SIL
SON, WOO-CHAN
author_sort JUNG, SUNYOUNG
collection PubMed
description The Sleeping Beauty transposon system is used as a tool for insertional mutagenesis and oncogenesis. However, little is known about the exact histological phenotype of the tumors induced. Thus, we used immunohistochemical markers to enable histological identification of the type of tumor induced by subcutaneous injection of the HRAS, c-Myc and shp53 oncogenes in female C57BL/6 mice. The tumor was removed when it reached 100 mm(3) in volume. Subsequently, we used 13 immunohistochemical markers to histologically identify the tumor type. The results suggested that the morphology of the tumor was similar to that of sarcomatoid carcinoma.
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spelling pubmed-36217332013-04-10 Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin JUNG, SUNYOUNG RO, SIMON WEONSANG JUNG, GEUNYOUNG JU, HYE-LIM YU, EUN-SIL SON, WOO-CHAN Oncol Rep Articles The Sleeping Beauty transposon system is used as a tool for insertional mutagenesis and oncogenesis. However, little is known about the exact histological phenotype of the tumors induced. Thus, we used immunohistochemical markers to enable histological identification of the type of tumor induced by subcutaneous injection of the HRAS, c-Myc and shp53 oncogenes in female C57BL/6 mice. The tumor was removed when it reached 100 mm(3) in volume. Subsequently, we used 13 immunohistochemical markers to histologically identify the tumor type. The results suggested that the morphology of the tumor was similar to that of sarcomatoid carcinoma. D.A. Spandidos 2013-04 2013-01-31 /pmc/articles/PMC3621733/ /pubmed/23380875 http://dx.doi.org/10.3892/or.2013.2264 Text en Copyright © 2013, 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
JUNG, SUNYOUNG
RO, SIMON WEONSANG
JUNG, GEUNYOUNG
JU, HYE-LIM
YU, EUN-SIL
SON, WOO-CHAN
Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin
title Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin
title_full Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin
title_fullStr Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin
title_full_unstemmed Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin
title_short Sleeping Beauty transposon system harboring HRAS, c-Myc and shp53 induces sarcomatoid carcinomas in mouse skin
title_sort sleeping beauty transposon system harboring hras, c-myc and shp53 induces sarcomatoid carcinomas in mouse skin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621733/
https://www.ncbi.nlm.nih.gov/pubmed/23380875
http://dx.doi.org/10.3892/or.2013.2264
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