Kub5-Hera(RPRD1B) deficiency promotes “BRCAness” and vulnerability to PARP inhibition in BRCA-proficient breast cancers
File(s)Motea et al CCR 2018 Accepted .pdf (1.86 MB)
Accepted version
Author(s)
Type
Journal Article
Abstract
Purpose: Identification of novel strategies to expand the use of PARP inhibitors beyond BRCA deficiency is of great interest in personalized medicine. Here, we investigated the unannotated role of Kub5-Hera(RPRD1B) (K-H) in homologous recombination (HR) repair and its potential clinical significance in targeted cancer therapy. Experimental Design: Functional characterization of K-H alterations on HR repair of double-strand breaks (DSB) were assessed by targeted gene silencing, plasmid reporter assays, immunofluorescence, and Western blots. Cell survival with PARP inhibitors was evaluated through colony-forming assays and statistically analyzed for correlation with K-H expression in various BRCA1/2 nonmutated breast cancers. Gene expression microarray/qPCR analyses, chromatin immunoprecipitation, and rescue experiments were used to investigate molecular mechanisms of action. Results: K-H expression loss correlates with rucaparib LD50 values in a panel of BRCA1/2 nonmutated breast cancers. Mechanistically, K-H depletion promotes BRCAness, where extensive upregulation of PARP1 activity was required for the survival of breast cancer cells. PARP inhibition in these cells led to synthetic lethality that was rescued by wild-type K-H reexpression, but not by a mutant K-H (p.R106A) that weakly binds RNAPII. K-H mediates HR by facilitating recruitment of RNAPII to the promoter region of a critical DNA damage response and repair effector, cyclin-dependent kinase 1 (CDK1). Conclusions: Cancer cells with low K-H expression may have exploitable BRCAness properties that greatly expand the use of PARP inhibitors beyond BRCA mutations. Our results suggest that aberrant K-H alterations may have vital translational implications in cellular responses/survival to DNA damage, carcinogenesis, and personalized medicine. (C) 2018 AACR.
Date Issued
2018-12-15
Date Acceptance
2018-08-09
Citation
Clinical Cancer Research, 2018, 24 (24), pp.6459-6470
ISSN
1078-0432
Publisher
American Association for Cancer Research
Start Page
6459
End Page
6470
Journal / Book Title
Clinical Cancer Research
Volume
24
Issue
24
Copyright Statement
©2018 American Association for Cancer Research.
Identifier
https://clincancerres.aacrjournals.org/content/24/24/6459
Subjects
Animals
Breast Neoplasms
CDC2 Protein Kinase
Cell Cycle Proteins
Cell Line, Tumor
DNA Damage
Disease Models, Animal
Female
Gene Expression Regulation, Neoplastic
Genes, BRCA1
Genes, BRCA2
Genes, Reporter
Humans
Mice
Mutation
Neoplasm Proteins
Poly(ADP-ribose) Polymerase Inhibitors
Poly(ADP-ribose) Polymerases
Promoter Regions, Genetic
Synthetic Lethal Mutations
Xenograft Model Antitumor Assays
Cell Line, Tumor
Animals
Humans
Mice
Breast Neoplasms
DNA Damage
Disease Models, Animal
Poly(ADP-ribose) Polymerases
CDC2 Protein Kinase
Cell Cycle Proteins
Neoplasm Proteins
Xenograft Model Antitumor Assays
Gene Expression Regulation, Neoplastic
Mutation
Genes, BRCA1
Genes, BRCA2
Genes, Reporter
Female
Promoter Regions, Genetic
Poly(ADP-ribose) Polymerase Inhibitors
Synthetic Lethal Mutations
1112 Oncology and Carcinogenesis
Oncology & Carcinogenesis
Notes
researcherid-numbers: Boothman, David/Q-7776-2019 unique-id: ISI:000453267600037
Publication Status
Published
Article Number
24
Date Publish Online
2018-08-14