DNA C-circles are specific and quantifiable markers of alternative-lengthening-of-telomeres activity

被引:377
作者
Henson, Jeremy D. [1 ]
Cao, Ying [1 ]
Huschtscha, Lily I. [1 ]
Chang, Andy C. [1 ]
Au, Amy Y. M. [1 ]
Pickett, Hilda A. [1 ]
Reddel, Roger R. [1 ]
机构
[1] Univ Sydney, Childrens Med Res Inst, Sydney, NSW 2006, Australia
关键词
HUMAN CELL-LINE; ALT CELLS; MECHANISM; RECOMBINATION; MAINTENANCE; COMPLEX; ABSENCE; TUMORS;
D O I
10.1038/nbt.1587
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Alternative lengthening of telomeres (ALT)(1) is likely to be an important target for anticancer treatment as similar to 10% of cancers depend on this telomere maintenance mechanism for continued growth(2), and inhibition of ALT can cause cellular senescence(3). However, no ALT inhibitors have been developed for therapeutic use because of the lack of a suitable ALT activity assay and of known ALT-specific target molecules. Here we show that partially single-stranded telomeric (CCCTAA)(n) DNA circles (C-circles) are ALT specific. We provide an assay that is rapidly and linearly responsive to ALT activity and that is suitable for screening for ALT inhibitors. We detect C-circles in blood from ALT(+) osteosarcoma patients, suggesting that the C-circle assay (CC assay) may have clinical utility for diagnosis and management of ALT(+) tumors.
引用
收藏
页码:1181 / U148
页数:6
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