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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Frequency of mesenchymal-epithelial transition factor gene (MET) and the catalytic subunit of phosphoinositide-3-kinase (PIK3CA) copy number elevation and correlation with outcome in patients with early stage breast cancer
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Frequency of mesenchymal-epithelial transition factor gene (MET) and the catalytic subunit of phosphoinositide-3-kinase (PIK3CA) copy number elevation and correlation with outcome in patients with early stage breast cancer

机译:早期乳腺癌患者间质-上皮转化因子基因(MET)和磷酸肌醇-3-激酶催化亚基(PIK3CA)拷贝数升高的频率及其与预后的关系

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BACKGROUND: The current study was conducted to determine the frequency and association between recurrence-free survival (RFS) and MET and catalytic subunit of phosphoinositide-3-kinase (PIK3CA) copy number elevations in patients with early stage breast cancer. METHODS: Tumor DNA was extracted from 971 formalin-fixed, paraffin-embedded early breast cancers for molecular inversion probes arrays. Data were segmented using the single-nucleotide polymorphism (SNP)-FASST2 segmentation algorithm. Copy number gains were called when the copy number of each segment was greater than 2.3 or 1.7, respectively. RFS was estimated by the Kaplan-Meier method. Cox proportional hazards models were fit to determine independent associations between copy number and RFS. RESULTS: Of the 971 tumors studied, 82 (8.44%) and 134 (13.8%) had an elevation of the MET or PIK3CA copy number, respectively, and 25.6% of tumors with a MET copy number elevation had a PIK3CA copy number elevation. Patients with either a MET or PI3KCA high copy number tended to have poorer prognostic features (larger tumor size, higher tumor grade, and hormone receptor negativity). Both MET and PIK3CA high copy numbers were more likely to occur in patients with triple receptor-negative disease (P = .019 and P < .001, respectively). At a median follow-up of 7.4 years, there were 252 cases of disease recurrence. The 5-year RFS rates were 63.5% and 83.1% for MET high copy number and MET normal/low copy number, respectively (P = .06) and 73.1%, and 82.3% for PIK3CA high copy number and PIK3CA normal/low copy number, respectively (P = .15). A high copy number for either gene was not found to be an independent predictor of RFS. CONCLUSIONS: A high copy number of MET or PIK3CA was found to be associated with poorer prognostic features and triple receptor-negative disease. Coamplification was frequent. Patients with tumors with high MET copy numbers tended to have a worse RFS. Cancer 2013. (c) 2012 American Cancer Society.
机译:背景:目前的研究是为了确定早期乳腺癌患者的无复发生存期(RFS)和MET与磷酸肌醇-3-激酶(PIK3CA)的催化亚基拷贝数升高之间的频率和相关性。方法:从971个福尔马林固定,石蜡包埋的早期乳腺癌中提取肿瘤DNA,用于分子倒置探针阵列。使用单核苷酸多态性(SNP)-FASST2分割算法对数据进行分割。当每个段的拷贝数分别大于2.3或1.7时,将调用拷贝数增益。 RFS是通过Kaplan-Meier方法估算的。考克斯比例风险模型适合确定拷贝数和RFS之间的独立关联。结果:在研究的971例肿瘤中,MET或PIK3CA拷贝数升高的分别为82(8.44%)和134(13.8%),MET拷贝数升高的肿瘤中有25.6%的PIK3CA拷贝数升高。 MET或PI3KCA高拷贝数的患者往往具有较差的预后特征(更大的肿瘤大小,更高的肿瘤等级和激素受体阴性)。 MET和PIK3CA高拷贝数在三联受体阴性疾病患者中更可能发生(分别为P = .019和P <.001)。在7.4年的中位随访中,有252例疾病复发。 MET高拷贝数和MET正常/低拷贝数的5年RFS率分别为63.5%和83.1%(P = .06)和PIK3CA高拷贝数和PIK3CA正常/低拷贝数的73.1%和82.3%数(P = .15)。没有发现任一个基因的高拷贝数是RFS的独立预测因子。结论:发现高拷贝数的MET或PIK3CA与较差的预后特征和三受体阴性疾病有关。放大频繁。 MET拷贝数高的肿瘤患者的RFS较差。癌症,2013年。(c)2012年美国癌症协会。

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