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ATM 下调与散发性乳腺癌不良预后相关。

ATM down-regulation is associated with poor prognosis in sporadic breast carcinomas.

机构信息

NeoGene Laboratory, Department of Urology, São Paulo State University, Botucatu.

出版信息

Ann Oncol. 2014 Jan;25(1):69-75. doi: 10.1093/annonc/mdt421. Epub 2013 Nov 26.

Abstract

BACKGROUND

Ataxia 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 METHODS

ATM 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.

RESULTS

Low 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).

CONCLUSIONS

The 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.

摘要

背景

已报道在散发性乳腺癌(BC)中存在 ATM 基因突变表达;然而,ATM 失调控的预后价值和机制仍不清楚。

方法

通过实时定量 PCR(RT-qPCR)评估 52 例 BC 和 3 例正常乳腺样本中的 ATM 和 miRNA(miR-26a、miR-26b、miR-203、miR-421、miR-664、miR-576-5p 和 miR-18a)表达水平。免疫组织化学检测 968 例 BC 和 35 例相邻正常乳腺组织中的 ATM 蛋白表达。通过阵列比较基因组杂交(aCGH)检测 42 例肿瘤中的 ATM 拷贝数改变。

结果

低 ATM 水平与肿瘤分级相关。ATM 蛋白表达缺失与远处转移(P<0.001)、降低的无病生存(DFS,P<0.001)和癌症特异性生存(CSS,P<0.001)相关。多变量分析表明 ATM 蛋白表达是 DFS(P=0.001,HR=0.579)和 CSS(P=0.001,HR=0.554)的独立预后标志物。在 12%的肿瘤中检测到 ATM 拷贝数缺失,并与较低的 mRNA 水平相关。在 36.5%的病例中检测到 miR-421 过表达,其 ATM 转录水平较低(P=0.075,r=-0.249)。

结论

数据表明 ATM 蛋白表达是散发性 BC 的独立预后标志物。基因拷贝数缺失和 miR-421 过表达可能参与了 BC 中 ATM 的失调控。

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