APRIN is a cell cycle specific BRCA2-interacting protein required for genome integrity and a predictor of outcome after chemotherapy in breast cancer
被引:57
作者:
Brough, Rachel
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Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Canc Res UK Gene Funct & Regulat Grp, London, EnglandInst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Brough, Rachel
[1
,2
]
Bajrami, Ilirjana
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Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Canc Res UK Gene Funct & Regulat Grp, London, EnglandInst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Bajrami, Ilirjana
[1
,2
]
Vatcheva, Radost
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Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, EnglandInst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Vatcheva, Radost
[1
]
Natrajan, Rachael
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Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, EnglandInst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Natrajan, Rachael
[1
]
Reis-Filho, Jorge S.
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Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, EnglandInst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Reis-Filho, Jorge S.
[1
]
Lord, Christopher J.
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Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, EnglandInst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Lord, Christopher J.
[1
]
Ashworth, Alan
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Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Canc Res UK Gene Funct & Regulat Grp, London, EnglandInst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
Ashworth, Alan
[1
,2
]
机构:
[1] Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
[2] Canc Res UK Gene Funct & Regulat Grp, London, England
BRCA2;
breast cancer;
DNA repair;
SISTER-CHROMATID COHESION;
STALLED REPLICATION FORKS;
DOUBLE-STRAND BREAK;
DNA-DAMAGE;
ALLELIC LOSS;
BASAL-LIKE;
BRCA2;
REPAIR;
EXPRESSION;
GENE;
D O I:
10.1038/emboj.2011.490
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:
Mutations in BRCA2 confer an increased risk of cancer development, at least in part because the BRCA2 protein is required for the maintenance of genomic integrity. Here, we use proteomic profiling to identify APRIN (PDS5B), a cohesion-associated protein, as a BRCA2-associated protein. After exposure of cells to hydroxyurea or aphidicolin, APRIN and other cohesin components associate with BRCA2 in early S-phase. We demonstrate that APRIN expression is required for the normal response to DNA-damaging agents, the nuclear localisation of RAD51 and BRCA2 and efficient homologous recombination. The clinical significance of these findings is indicated by the observation that the BRCA2/APRIN interaction is compromised by BRCA2 missense variants of previously unknown significance and that APRIN expression levels are associated with histological grade in breast cancer and the outcome of breast cancer patients treated with DNA-damaging chemotherapy. The EMBO Journal (2012) 31, 1160-1176. doi: 10.1038/emboj.2011.490; Published online 31 January 2012