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

被引:3
|
作者
Saito, Megumi [1 ]
Kagawa, Naoko [2 ,3 ]
Okumura, Kazuhiro [1 ]
Munakata, Haruka [1 ]
Isogai, Eriko [1 ]
Fukagawa, Tatsuo [2 ,3 ,4 ]
Wakabayashi, Yuichi [1 ]
机构
[1] Chiba Canc Ctr Res Inst, Dept Carcinogenesis Res, Div Expt Anim Res, Chiba, Japan
[2] Natl Inst Genet, Dept Mol Genet, Mishima, Shizuoka, Japan
[3] Grad Univ Adv Studies, Mishima, Shizuoka, Japan
[4] Osaka Univ, Lab Chromosome Biol, Grad Sch Frontier Biosci, Suita, Osaka, Japan
基金
日本学术振兴会;
关键词
CENP; malignant conversion; mouse models; papilloma; two-stage skin carcinogenesis; CENTROMERE PROTEIN-A; MALIGNANT PROGRESSION; EXPRESSION; CELLS; GENE; DISRUPTION; PROMOTION; COMPLEX; CANCER; OVEREXPRESSION;
D O I
10.1111/cas.14533
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 ofCENP-50/Uhas been reported in many types of cancers. However, asCenp-50/U-deficient mice die during early embryogenesis, its functions remain poorly understood in vivo. To investigate the role ofCenp-50/Uin skin carcinogenesis, we generatedCenp-50/Uconditional 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 inCenp-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 thatCenp-50/Uexpression levels in papillomas were significantly higher than in carcinomas. These results suggest thatCenp-50/Ufunctions mainly in early papilloma development and it has little effect on malignant conversion.
引用
收藏
页码:2850 / 2860
页数:11
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