Chromatin to Clinic: The Molecular Rationale for PARP1 Inhibitor Function

被引:113
|
作者
Feng, Felix Y. [1 ,2 ,3 ]
De Bono, Johann S. [4 ]
Rubin, Mark A. [5 ,6 ,7 ,8 ,9 ]
Knudsen, Karen E. [10 ,11 ,12 ,13 ]
机构
[1] Univ Michigan, Michigan Ctr Translat Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[4] Royal Marsden NHS Fdn Trust, Prostate Canc Targeted Therapy Grp, Sutton SM2 5PT, Surrey, England
[5] Weill Cornell Med Coll, Inst Precis Med, New York, NY 10021 USA
[6] NewYork Presbyterian Hosp, New York, NY 10021 USA
[7] Weill Cornell Med Coll, Dept Pathol & Lab Med, New York, NY 10021 USA
[8] Weill Cornell Med Coll, Dept Urol, New York, NY 10021 USA
[9] Weill Cornell Med Coll, Meyer Canc Ctr, New York, NY 10021 USA
[10] Thomas Jefferson Univ, Dept Canc Biol, Philadelphia, PA 19107 USA
[11] Thomas Jefferson Univ, Dept Urol, Philadelphia, PA 19107 USA
[12] Thomas Jefferson Univ, Dept Radiat Oncol, Philadelphia, PA 19107 USA
[13] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
关键词
NF-KAPPA-B; OLAPARIB MAINTENANCE THERAPY; POLY(ADP-RIBOSE) POLYMERASE; HOMOLOGOUS RECOMBINATION; DNA-DAMAGE; GENE-EXPRESSION; OVARIAN-CANCER; REPAIR; ACTIVATION; CELLS;
D O I
10.1016/j.molcel.2015.04.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Poly(ADP-ribose) polymerase 1 (PARP1) inhibitors were recently shown to have potential clinical impact in a number of disease settings, particularly as related to cancer therapy, treatment for cardiovascular dysfunction, and suppression of inflammation. The molecular basis for PARP1 inhibitor function is complex, and appears to depend on the dual roles of PARP1 in DNA damage repair and transcriptional regulation. Here, the mechanisms by which PARP-1 inhibitors elicit clinical response are discussed, and strategies for translating the preclinical elucidation of PARP-1 function into advances in disease management are reviewed.
引用
收藏
页码:925 / 934
页数:10
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