Format

Send to

Choose Destination
Breast Cancer Res Treat. 2011 May;127(1):273-81. doi: 10.1007/s10549-010-1199-y. Epub 2010 Nov 11.

Poly(ADP-ribose) polymerase-1 mRNA expression in human breast cancer: a meta-analysis.

Author information

1
Département d'Oncologie Médicale and U891 INSERM, Centre de Recherche en Cancérologie de Marseille, Institut Paoli-Calmettes, 232 Bd. Ste-Marguerite, 13009 Marseille, France. goncalvesa@marseille.fnclcc.fr

Abstract

Although poly(ADP-ribose) polymerase-1 (PARP1) inhibition is a recent promising therapy in breast cancer, PARP1 expression in this disease is not known. Using DNA microarray and array-based comparative genomic hybridization (arrayCGH), we examined PARP1 mRNA expression and copy number alterations in 326 invasive breast cancer samples and normal breast (NB) samples. A meta-analysis was performed on a large public retrospective gene expression data set (n = 2,485) to analyze correlation between PARP1 mRNA expression and molecular subtypes and clinico-pathological parameters. PARP1 was overexpressed in 58% of cancers, and its expression was heterogeneous between tumors. ArrayCGH data revealed an association between mRNA overexpression and gain/amplification at the PARP1 locus (P < 1.0E-8). Meta-analysis showed that PARP1 expression was higher in basal breast cancers (P < 1.0E-72), but overexpression was also found in other subtypes. PARP1 expression correlated with high grade, medullary histological type, tumor size, and worse metastasis-free survival (MFS; HR = 1.12 [1.04-1.22], P = 0.004) and overall survival (OS; HR = 1.16 [1.04-1.29], P = 0.006). In multivariate analysis, PARP1 expression had an independent prognostic value for MFS, which was restricted to patients untreated with any adjuvant chemotherapy. These data demonstrate overexpression of PARP1 in a large number of breast cancers and support the development of PARP inhibitors in basal subtype, but also potentially in other breast cancer subtypes.

Comment in

PMID:
21069454
DOI:
10.1007/s10549-010-1199-y
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Springer
Loading ...
Support Center