三阴性乳腺癌的全基因组miRNA、基因和甲基化分析,以确定与淋巴结转移相关的变化

Kelly A. Avery-Kiejda , Andrea Mathe , Rodney J. Scott
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引用次数: 9

摘要

三阴性乳腺癌(TNBC)是一种特别重要的乳腺癌亚型,具有侵袭性的临床表型,与较高的转移可能性相关。该亚型的特点是缺乏雌激素(ER)和孕激素(PR)受体,以及人表皮生长因子受体2 (HER2/HER neu)。这三种受体的缺失大大减少了TNBC患者的靶向治疗选择,因此,迫切需要确定新的治疗靶点。在这里,我们提供了关于多平台数据集设计的详细信息,该数据集描述了tnbc、匹配的正常邻近组织和匹配的淋巴结转移中miRNA(通过微阵列评估,GSE38167)、基因表达(通过微阵列评估,GSE61723)以及甲基化(通过Illumina HM450K BeadChip评估,GSE78751)的全基因组评估。使用这个多平台数据集可能会发现TNBC中涉及淋巴结转移进展的新标志物和关键途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genome-wide miRNA, gene and methylation analysis of triple negative breast cancer to identify changes associated with lymph node metastases

Genome-wide miRNA, gene and methylation analysis of triple negative breast cancer to identify changes associated with lymph node metastases

Genome-wide miRNA, gene and methylation analysis of triple negative breast cancer to identify changes associated with lymph node metastases

Triple negative breast cancer (TNBC) is a particularly important breast cancer subtype with an aggressive clinical phenotype that is associated with a higher likelihood of metastasis. This subtype is characterized by an absence of the estrogen (ER) and progesterone (PR) receptors, as well as the human epidermal growth factor receptor 2 (HER2/HER neu). The absence of the three receptors significantly reduces targeted treatment options for patients with TNBC and as such, there is an urgent need to identify novel treatment targets. Here, we provide detailed information regarding the design of a multi-platform dataset that describes genome-wide assessment of miRNA (assessed by microarray, GSE38167) and gene expression (assessed by microarray, GSE61723), as well as methylation (assessed by Illumina HM450K BeadChip, GSE78751) in TNBCs, matched normal adjacent tissues and matched lymph node metastases. The use of this multi-platform dataset is likely to uncover novel markers and key pathways involved in progression to lymph node metastasis in TNBC.

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