Chfr is required for tumor suppression and Aurora A regulation

Xiaochun Yu, Katherine Minter-Bykhouse, Liviu Malureanu, Wei Meng Zhao, Dongwei Zhang, Carolin J. Merkle, Irene M. Ward, Hideyuki Saya, Guowei Fang, Jan Van Deursen, Junjie Chen

研究成果: Article査読

174 被引用数 (Scopus)


Tumorigenesis is a consequence of loss of tumor suppressors and activation of oncogenes. Expression of the mitotic checkpoint protein Chfr is lost in 20-50% of primary tumors and tumor cell lines. To explore whether downregulation of Chfr contributes directly to tumorigenesis, we generated Chfr knockout mice. Chfr-deficient mice are cancer-prone, develop spontaneous tumors and have increased skin tumor incidence after treatment with dimethylbenz(a)anthracene. Chfr deficiency leads to chromosomal instability in embryonic fibroblasts and regulates the mitotic kinase Aurora A, which is frequently upregulated in a variety of tumors. Chfr physically interacts with Aurora A and ubiquitinates Aurora A both in vitro and in vivo. Collectively, our data suggest that Chfr is a tumor suppressor and ensures chromosomal stability by controlling the expression levels of key mitotic proteins such as Aurora A.

ジャーナルNature genetics
出版ステータスPublished - 2005 4月

ASJC Scopus subject areas

  • 遺伝学


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