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Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer
The c-mos proto-oncogene was one of the first proto-oncogenes to be cloned. Apart from its role in meiosis, many efforts have been made to illuminate the mechanisms by which c-mos might acts as an oncogene. Increased Mos expression was found in most human tumor tissues. However, a detailed role of c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6139997/ https://www.ncbi.nlm.nih.gov/pubmed/30229128 http://dx.doi.org/10.1016/j.dib.2018.08.129 |
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author | Chen, Zhengxi Qiao, Ju Wang, Qirui Xiao, Qian |
author_facet | Chen, Zhengxi Qiao, Ju Wang, Qirui Xiao, Qian |
author_sort | Chen, Zhengxi |
collection | PubMed |
description | The c-mos proto-oncogene was one of the first proto-oncogenes to be cloned. Apart from its role in meiosis, many efforts have been made to illuminate the mechanisms by which c-mos might acts as an oncogene. Increased Mos expression was found in most human tumor tissues. However, a detailed role of c-mos in tumor progression remains unknown. In this study, we analyzed online databases to find out the correlation between Mos expression and poor survival rates in human cancer patients. Then, we crossed c-mos knockout mice with Apc(Min) or Kras(G12D) mice to generate intestinal cancer model and lung cancer model, respectively. Tumor progression was monitored, and the influence of c-mos deficiency on cancer formation was investigated. |
format | Online Article Text |
id | pubmed-6139997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61399972018-09-18 Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer Chen, Zhengxi Qiao, Ju Wang, Qirui Xiao, Qian Data Brief Proteomics The c-mos proto-oncogene was one of the first proto-oncogenes to be cloned. Apart from its role in meiosis, many efforts have been made to illuminate the mechanisms by which c-mos might acts as an oncogene. Increased Mos expression was found in most human tumor tissues. However, a detailed role of c-mos in tumor progression remains unknown. In this study, we analyzed online databases to find out the correlation between Mos expression and poor survival rates in human cancer patients. Then, we crossed c-mos knockout mice with Apc(Min) or Kras(G12D) mice to generate intestinal cancer model and lung cancer model, respectively. Tumor progression was monitored, and the influence of c-mos deficiency on cancer formation was investigated. Elsevier 2018-08-31 /pmc/articles/PMC6139997/ /pubmed/30229128 http://dx.doi.org/10.1016/j.dib.2018.08.129 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Proteomics Chen, Zhengxi Qiao, Ju Wang, Qirui Xiao, Qian Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer |
title | Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer |
title_full | Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer |
title_fullStr | Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer |
title_full_unstemmed | Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer |
title_short | Data on tumor progression of c-mos deficiency in murine models of Kras(G12D) lung and Apc(Min) colorectal cancer |
title_sort | data on tumor progression of c-mos deficiency in murine models of kras(g12d) lung and apc(min) colorectal cancer |
topic | Proteomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6139997/ https://www.ncbi.nlm.nih.gov/pubmed/30229128 http://dx.doi.org/10.1016/j.dib.2018.08.129 |
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