Elevated CXorf67 Expression in PFA Ependymomas Suppresses DNA Repair and Sensitizes to PARP Inhibitors

被引:40
作者
Han, Jichang [1 ,2 ]
Yu, Meng [1 ,2 ]
Bai, Yiqin [1 ]
Yu, Jianzhong [3 ]
Jin, Fei [1 ]
Li, Chen [4 ]
Zeng, Rong [2 ,4 ]
Peng, Jinghong [1 ]
Li, Ao [5 ]
Song, Xiaomin [1 ]
Li, Hao [3 ]
Wu, Dianqing [5 ]
Li, Lin [1 ,2 ,6 ]
机构
[1] Chinese Acad Sci, Univ Chinese Acad Sci, State Key Lab Mol Biol, Inst Biochem & Cell Biol,CAS Ctr Excellence Mol C, Shanghai 200031, Peoples R China
[2] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
[3] Fudan Univ, Dept Neurosurg, Childrens Hosp, Shanghai 201102, Peoples R China
[4] Chinese Acad Sci, CAS Ctr Excellence Mol Cell Sci, Inst Biochem & Cell Biol, CAS Key Lab Syst Biol, Shanghai 200031, Peoples R China
[5] Yale Sch Med, Dept Pharmacol, New Haven, CT 06510 USA
[6] Univ Chinese Acad Sci, Sch Life Sci, Hangzhou Inst Adv Study, Hangzhou 310024, Peoples R China
基金
中国国家自然科学基金;
关键词
HOMOLOGOUS RECOMBINATION; DAMAGE RESPONSE; CHEMOTHERAPY; COMPONENT; TUMORS; BRCA2;
D O I
10.1016/j.ccell.2020.10.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ependymoma is the third most common pediatric tumor with posterior fossa group A (PFA) being its most aggressive subtype. Ependymomas are generally refractory to chemotherapies and thus lack any effective treatment. Here, we report that elevated expression of CXorf67 (chromosome X open reading frame 67), which frequently occurs in PFA ependymomas, suppresses homologous recombination (HR)-mediated DNA repair. Mechanistically, CXorf67 interacts with PALB2 and inhibits PALB2-BRCA2 interaction, thereby inhibiting HR repair. Concordantly, tumor cells with high CXorf67 expression levels show increased sensitivity to poly(ADP-ribose) polymerase (PARP) inhibitors, especially when combined with radiotherapy. Thus, our findings have revealed a role of CXorf67 in HR repair and suggest that combination of PARP inhibitors with radiotherapy could be an effective treatment option for PFA ependymomas.
引用
收藏
页码:844 / +
页数:20
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