ATM down-regulation is associated with poor prognosis in sporadic breast carcinomas |
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Affiliation: | 1. NeoGene Laboratory, Department of Urology, São Paulo State University, Botucatu;2. A. C. Camargo Cancer Center, São Paulo;3. Laboratory of Biomedical Vibrational Spectroscopy (LEVB), Institute of Research and Development, IP&D, Paraíba Valley University, São José dos Campos;4. Department of Pathology, São Paulo State University, Botucatu;5. Department of Senology, Amaral Carvalho Hospital, Jaú;6. Department of Pathology, A. C. Camargo Cancer Center, São Paulo, Brazil |
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Abstract: | BackgroundAtaxia telangiectasia-mutated (ATM) gene downexpression has been reported in sporadic breast carcinomas (BC); however, the prognostic value and mechanisms of ATM deregulation remain unclear.Patients and methodsATM and miRNAs (miR-26a, miR-26b, miR-203, miR-421, miR-664, miR-576-5p and miR-18a) expression levels were evaluated by quantitative real-time PCR (RT-qPCR) in 52 BC and 3 normal breast samples. ATM protein expression was assessed by immunohistochemistry in 968 BC and 35 adjacent normal breast tissues. ATM copy number alteration was detected by array comparative genomic hybridization (aCGH) in 42 tumours.ResultsLow ATM levels were associated with tumour grade. Absence of ATM protein expression was associated with distant metastasis (P < 0.001), reduced disease-free survival (DFS, P < 0.001) and cancer-specific survival (CSS, P < 0.001). Multivariate analysis indicated ATM protein expression as an independent prognostic marker for DFS (P = 0.001, HR = 0.579) and CSS (P = 0.001, HR = 0.554). ATM copy number loss was detected in 12% of tumours and associated with lower mRNA levels. miR-421 over-expression was detected in 36.5% of cases which exhibit lower ATM transcript levels (P = 0.075, r = -0.249).ConclusionsThe data suggest that ATM protein expression is an independent prognostic marker in sporadic BC. Gene copy number loss and miR-421 over-expression may be involved in ATM deregulation in BC. |
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