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  2. CENP-50 is required for papilloma development in the two-stage skin carcinogenesis model

CENP-50 is required for papilloma development in the two-stage skin carcinogenesis model

  • Cancer Sci. 2020 Aug;111(8):2850-2860. doi: 10.1111/cas.14533.
Megumi Saito 1 Naoko Kagawa 2 Kazuhiro Okumura 1 Haruka Munakata 1 Eriko Isogai 1 Tatsuo Fukagawa 2 3 Yuichi Wakabayashi 1
Affiliations

Affiliations

  • 1 Department of Carcinogenesis Research, Division of Experimental Animal Research, Chiba Cancer Center Research Institute, Chiba, Japan.
  • 2 Department of Molecular Genetics, National Institute of Genetics and The Graduate University for Advanced Studies, Mishima, Japan.
  • 3 Laboratory of Chromosome Biology, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.
Abstract

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 (K14CreER -Cenp-50/Ufl/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.

Keywords

CENP; malignant conversion; mouse models; papilloma; two-stage skin carcinogenesis.

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