Cargando…
CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model
CENP‐50/U is a component of the CENP‐O complex (CENP‐O/P/Q/R/U) and localizes to the centromere throughout the cell cycle. Aberrant expression of CENP‐50/U has been reported in many types of cancers. However, as Cenp‐50/U‐deficient mice die during early embryogenesis, its functions remain poorly und...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419024/ https://www.ncbi.nlm.nih.gov/pubmed/32535988 http://dx.doi.org/10.1111/cas.14533 |
_version_ | 1783569801217572864 |
---|---|
author | Saito, Megumi Kagawa, Naoko Okumura, Kazuhiro Munakata, Haruka Isogai, Eriko Fukagawa, Tatsuo Wakabayashi, Yuichi |
author_facet | Saito, Megumi Kagawa, Naoko Okumura, Kazuhiro Munakata, Haruka Isogai, Eriko Fukagawa, Tatsuo Wakabayashi, Yuichi |
author_sort | Saito, Megumi |
collection | PubMed |
description | CENP‐50/U is a component of the CENP‐O complex (CENP‐O/P/Q/R/U) and localizes to the centromere throughout the cell cycle. Aberrant expression of CENP‐50/U has been reported in many types of cancers. However, as Cenp‐50/U‐deficient mice die during early embryogenesis, its functions remain poorly understood in vivo. To investigate the role of Cenp‐50/U in skin carcinogenesis, we generated Cenp‐50/U conditional knockout (K14Cre(ER)‐Cenp‐50/U (fl/fl)) mice and subjected them to the 7,12‐dimethylbenz(a)anthracene (DMBA)/terephthalic acid (TPA) chemical carcinogenesis protocol. As a result, early‐stage papillomas decreased in Cenp‐50/U‐deficient mice. In contrast, Cenp‐50/U‐deficient mice demonstrated almost the same carcinoma incidence as control mice. Furthermore, mRNA expression analysis using DMBA/TPA‐induced papillomas and carcinomas revealed that Cenp‐50/U expression levels in papillomas were significantly higher than in carcinomas. These results suggest that Cenp‐50/U functions mainly in early papilloma development and it has little effect on malignant conversion. |
format | Online Article Text |
id | pubmed-7419024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74190242020-08-12 CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model Saito, Megumi Kagawa, Naoko Okumura, Kazuhiro Munakata, Haruka Isogai, Eriko Fukagawa, Tatsuo Wakabayashi, Yuichi Cancer Sci Original Articles CENP‐50/U is a component of the CENP‐O complex (CENP‐O/P/Q/R/U) and localizes to the centromere throughout the cell cycle. Aberrant expression of CENP‐50/U has been reported in many types of cancers. However, as Cenp‐50/U‐deficient mice die during early embryogenesis, its functions remain poorly understood in vivo. To investigate the role of Cenp‐50/U in skin carcinogenesis, we generated Cenp‐50/U conditional knockout (K14Cre(ER)‐Cenp‐50/U (fl/fl)) mice and subjected them to the 7,12‐dimethylbenz(a)anthracene (DMBA)/terephthalic acid (TPA) chemical carcinogenesis protocol. As a result, early‐stage papillomas decreased in Cenp‐50/U‐deficient mice. In contrast, Cenp‐50/U‐deficient mice demonstrated almost the same carcinoma incidence as control mice. Furthermore, mRNA expression analysis using DMBA/TPA‐induced papillomas and carcinomas revealed that Cenp‐50/U expression levels in papillomas were significantly higher than in carcinomas. These results suggest that Cenp‐50/U functions mainly in early papilloma development and it has little effect on malignant conversion. John Wiley and Sons Inc. 2020-07-06 2020-08 /pmc/articles/PMC7419024/ /pubmed/32535988 http://dx.doi.org/10.1111/cas.14533 Text en © 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Saito, Megumi Kagawa, Naoko Okumura, Kazuhiro Munakata, Haruka Isogai, Eriko Fukagawa, Tatsuo Wakabayashi, Yuichi CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model |
title | CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model |
title_full | CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model |
title_fullStr | CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model |
title_full_unstemmed | CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model |
title_short | CENP‐50 is required for papilloma development in the two‐stage skin carcinogenesis model |
title_sort | cenp‐50 is required for papilloma development in the two‐stage skin carcinogenesis model |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419024/ https://www.ncbi.nlm.nih.gov/pubmed/32535988 http://dx.doi.org/10.1111/cas.14533 |
work_keys_str_mv | AT saitomegumi cenp50isrequiredforpapillomadevelopmentinthetwostageskincarcinogenesismodel AT kagawanaoko cenp50isrequiredforpapillomadevelopmentinthetwostageskincarcinogenesismodel AT okumurakazuhiro cenp50isrequiredforpapillomadevelopmentinthetwostageskincarcinogenesismodel AT munakataharuka cenp50isrequiredforpapillomadevelopmentinthetwostageskincarcinogenesismodel AT isogaieriko cenp50isrequiredforpapillomadevelopmentinthetwostageskincarcinogenesismodel AT fukagawatatsuo cenp50isrequiredforpapillomadevelopmentinthetwostageskincarcinogenesismodel AT wakabayashiyuichi cenp50isrequiredforpapillomadevelopmentinthetwostageskincarcinogenesismodel |