Breast cancers with compromised DNA repair exhibit selective sensitivity to elesclomol

被引:19
作者
Alli, Elizabeth [1 ]
Ford, James M. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Med Oncol, Stanford, CA 93405 USA
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 93405 USA
关键词
Breast cancer; Basal-like breast cancer; Base-excision repair; Oxidative DNA damage; Elesclomol; Cancer therapy; MAMMARY EPITHELIAL-CELLS; POLY(ADP-RIBOSE) POLYMERASE; MOLECULAR PORTRAITS; TUMORS; CHEMOSENSITIVITY; GEMCITABINE; INHIBITION; CISPLATIN; BRCA1;
D O I
10.1016/j.dnarep.2012.02.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The basal-like subtype of breast cancers, including those that contain germline mutations in BRCA1, tend to be triple-negative (i.e. lack expression of estrogen and progesterone receptors and lack overexpression/amplification of the HER2/neu oncogene), which renders them relatively insensitive to existing "targeted" therapy. BRCA1-mutated and basal-like breast cancers harbor compromised ability for repairing oxidative DNA damage by the DNA base-excision repair pathway. We found that this defective repair mechanism predicts sensitivity to elesclomol, an experimental therapeutic that produces elevated levels of oxidative DNA damage. In conclusion, BRCA1-mutated and/or basal-like breast cancers may benefit from treatment regimens that include elesclomol. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:522 / 524
页数:3
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