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A breast cancer meta-analysis of two expression measures of chromosomal instability reveals a relationship with younger age at diagnosis and high risk histopathological variables

机译:两种染色体不稳定性表达指标的乳腺癌荟萃分析显示年龄与诊断年龄和高风险组织病理学变量有关

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摘要

Breast cancer in younger patients often presents with adverse histopathological features, including increased frequency of estrogen receptor negative and lymph node positive disease status. Chromosomal instability (CIN) is increasingly recognised as an important prognostic variable in solid tumours. In a breast cancer meta-analysis of 2423 patients we examine the relationship between clinicopathological parameters and two distinct chromosomal instability gene expression signatures in order to address whether younger age at diagnosis is associated with increased tumour genome instability. We find that CIN, assessed by the two independently derived CIN expression signatures, is significantly associated with increased tumour size, ER negative or HER2 positive disease, higher tumour grade and younger age at diagnosis in ER negative breast cancer. These data support the hypothesis that chromosomal instability may be a defining feature of breast cancer biology and clinical outcome.
机译:年轻患者中的乳腺癌通常表现出不利的组织病理学特征,包括雌激素受体阴性和淋巴结阳性的疾病状态增加。染色体不稳定性(CIN)被越来越多地认为是实体瘤中重要的预后变量。在一项针对2423位患者的乳腺癌荟萃分析中,我们检查了临床病理参数与两个不同的染色体不稳定性基因表达特征之间的关系,以便确定诊断时的年轻年龄是否与增加的肿瘤基因组不稳定性相关。我们发现,通过两个独立获得的CIN表达特征评估的CIN与ER阴性乳腺癌的肿瘤大小增加,ER阴性或HER2阳性疾病,更高的肿瘤等级和更年轻的年龄显着相关。这些数据支持以下假设:染色体不稳定可能是乳腺癌生物学和临床结果的决定性特征。

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