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High-throughput mass spectrometry and bioinformatics analysis of breast cancer proteomic data

机译:乳腺癌蛋白质组学数据的高通量质谱和生物信息学分析

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Data present here describe a comparative proteomic analysis among the malignant [primary breast tumor (PT) and axillary metastatic lymph nodes (LN)], and the non-tumor [contralateral (NCT) and adjacent (ANT)] breast tissues. Protein identification and quantification were performed through label-free mass spectrometry using a nano-liquid chromatography coupled to an electrospray ionization–mass spectrometry (nLC-ESI-MS/MS). The mass spectrometry proteomic data have been deposited to the ProteomeXchange Consortium via PRIDE partner repository with the dataset identifier PXD012431. A total of 462 differentially expressed proteins was identified among these tissues and was analyzed in six groups' comparisons (named NCTxANT, PTxNCT, PTxANT, LNxNCT, LNxANT and PTxLN). Proteins at 1.5 log2 fold change were submitted to the Ingenuity?Pathway Analysis (IPA) software version 2.3 (QIAGEN Inc.) to identify biological pathways, disease and function annotation, and interaction networks related to cancer biology. The detailed data present here provides information about the proteome alterations and their role on breast tumorigenesis. This information can lead to novel biological insights on cancer research. For further interpretation of these data, please see our research article ‘Quantitative label-free mass spectrometry using contralateral and adjacent breast tissues reveal differentially expressed proteins and their predicted impacts on pathways and cellular functions in breast cancer’ [2].
机译:此处提供的数据描述了恶性[原发性乳腺肿瘤(PT)和腋窝转移性淋巴结(LN)]以及非肿瘤[对侧(NCT)和邻近(ANT)]乳腺组织之间的比较蛋白质组学分析。蛋白质的鉴定和定量通过无标记质谱法进行,使用纳米液相色谱法与电喷雾电离质谱联用(nLC-ESI-MS / MS)。质谱蛋白质组学数据已通过PRIDE合作伙伴存储库以数据集标识符PXD012431存放到ProteomeXchange联盟。在这些组织中鉴定出总共462种差异表达的蛋白质,并在六组比较中进行了分析(命名为NCTxANT,PTxNCT,PTxANT,LNxNCT,LNxANT和PTxLN)。将1.5 log2倍变化的蛋白质提交给Ingenuity?Pathway Analysis(IPA)软件2.3版(QIAGEN Inc.),以鉴定生物学途径,疾病和功能注释以及与癌症生物学有关的相互作用网络。这里提供的详细数据提供了有关蛋白质组改变及其在乳腺肿瘤发生中的作用的信息。这些信息可以导致对癌症研究的新颖生物学见解。有关这些数据的进一步解释,请参见我们的研究文章“使用对侧和邻近乳腺组织的定量无标记质谱技术揭示差异表达的蛋白质及其对乳腺癌通路和细胞功能的预期影响” [2]。

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