首页> 外文期刊>International journal of applied mechanics >Integrative Analyses of Multilevel Omics Reveal Preneoplastic Breast to Possess a Molecular Landscape That is Globally Shared with Invasive Basal-Like Breast Cancer (Running Title: Molecular Landscape of Basal-Like Breast Cancer Progression)
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Integrative Analyses of Multilevel Omics Reveal Preneoplastic Breast to Possess a Molecular Landscape That is Globally Shared with Invasive Basal-Like Breast Cancer (Running Title: Molecular Landscape of Basal-Like Breast Cancer Progression)

机译:多级OMIC的整合分析显示肺骨塑乳房具有全球与侵袭性基础乳腺癌的全球分子景观(跑步标题:基础乳腺癌进展的分子景观)

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摘要

To characterize molecular changes accompanying the stepwise progression to breast cancer and to identify functional target pathways, we performed miRNA and RNA sequencing using MCF10A cell lines based model system that replicates the multi-step progression involving normal, preneoplastic, ductal carcinoma in situ, and invasive carcinoma cells, where the carcinoma most resemble the basal-like subgroup of human breast cancers. These analyses suggest that 70% of miRNA alterations occurred during the initial progression from normal to a preneoplastic stage. Most of these early changes reflected a global upregulation of miRNAs. This was consistent with a global increase in the miRNA-processing enzyme DICER, which was upregulated as a direct result of loss of miRNA let-7b-5p. Several oncogenic and tumor suppressor pathways were also found to change early, prior to histologic stigmata of cancer. Our finding that most genomic changes in the progression to basal-like breast cancer occurred in the earliest stages of histologic progression has implications for breast cancer prevention and selection of appropriate control tissues in molecular studies. Furthermore, in support of a functional significance of let-7b-5p loss, we found its low levels to predict poor disease-free survival and overall survival in breast cancer patients.
机译:表征伴随逐步进展到乳腺癌并鉴定功能靶途径的分子变化,我们使用基于MCF10A细胞系的模型系统进行了miRNA和RNA测序,该模型系统复制了涉及正常,营养的导管癌原位的多步进展,并侵入性癌细胞,癌细胞最像人类乳腺癌的基础亚组。这些分析表明,70%的miRNA改变在初始进展期间发生在正常到促塑性阶段。这些早期变化中的大部分都反映了miRNA的全球上调。这与miRNA加工酶DICER的全局增加一致,这是作为MiRNA Let-7B-5P损失的直接结果上调。在癌症的组织学恶性之前,还发现几种致癌和肿瘤抑制途径早期改变。我们认为,在组织学进展的最早阶段发生进展的大多数基因组变化发生在组织学进展的最早阶段具有对乳腺癌预防和选择分子研究中适当的对照组织的影响。此外,为了支持Let-7B-5P损失的功能性意义,我们发现其低水平以预测乳腺癌患者的无病的生存和整体生存率。

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