| 李晶 黄三钱 钟晶敏 欧阳取长 杨小红 吴晖 刘志红 曾亮.ER/PR阳性和阴性乳腺癌的定量蛋白质组学和生物信息学比较研究[J].现代生物医学进展英文版,2016,16(32):6387-6393. |
| ER/PR阳性和阴性乳腺癌的定量蛋白质组学和生物信息学比较研究 |
| Comparative Quantitative Proteomic and Bioinformatics Study on ER/PRPositive and Negative Breast Cancer |
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| DOI： |
| 中文关键词: 雌激素 孕激素 定量蛋白质组学 乳腺癌 |
| 英文关键词: Estrogen receptor Progesterone receptor Quantitative proteomics Breast cancer |
| 基金项目:湖南省科学技术厅科技计划专项项目（2014FJ6090） |
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| 中文摘要: |
| 目的：建立雌/孕激素受体(ER/PR)阴性和阳性乳腺癌的蛋白质表达谱，寻找ER/PR 阴性和阳性乳腺癌中差异表达蛋白，为
乳腺癌患者提供新的预后预测指标和治疗新靶点。方法：应用蛋白质组学iTRAQ技术建立ER/PR 阳性和阴性乳腺癌的蛋白质差
异表达谱，鉴定两组乳腺癌的差异表达蛋白，对部分差异表达蛋白进行生物信息学分析，包括蛋白功能注释和分类GO 分析和
KEGG通路分析。结果：应用iTRAQ 蛋白质组学技术对乳腺癌组织进行了蛋白组学分析，鉴定出ER/PR 阳性和阴性组间有差异
表达的蛋白4999 种，以ER/PR 阳性：ER/PR 阴性≥ 3为上调标准，确定ER/PR 阳性组上调蛋白101 种。以ER/PR 阳性：ER/PR 阴
性≤ 0.5 为下调标准，ER/PR 阳性组下调蛋白122 种。GO 分析结果显示ER/PR 受体阴性和阳性乳腺癌的差异表达蛋白的分子功
能、生物过程、细胞定位较为复杂，并且在上调蛋白和下调蛋白上存在分布差异。KEGG通路分析发现部分差异表达蛋白涉及201
条信号通路。结论：ER/PR阳性和阴性乳腺癌间存在差异表达蛋白，这些蛋白涉及复杂的分子功能、生物过程和信号通路。 |
| 英文摘要: |
| Objective:To establish differentially expressed proteins profiles for ER/PR negative and positive breast cancer and
provide new prognostic markers and therapeutic targets for patients with ER/PR positive breast cancer.Methods:By proteomic iTRAQ
technology, ER/PR positive and negative breast cancer protein expression profiles was established, differences of protein expression were
identified and parts of differential expression protein by bioinformatics analysis, including protein function annotation and GO
classification analysis and KEGG pathway analysis.Results:iTRAQ proteomic analysis of breast cancer tissue with identified ER/PR
positive and negative groups showed 4999 differentially expressed protein. While Ratio of ER/PR(+) /ER/PR (-) was higher than or equal
to 3 for standard cut, 101 up-regulated proteins in ER/PR positive group were identified. In ER/PR(+)/ER/PR (-) less than or equal to 0.5
for standard cut, 122 down-regulated proteins were identified in ER/PR positive group. The results of GO analysis showed that the
cellular composition, molecular function, biological process of differentially expressed proteins were complex between ER/PR positive
and negative breast cancer, and there were differences in the distribution of up-regulated proteins and down-regulation of proteins. KEGG
pathway analysis showed that differentially expressed proteins involved in 201 signal pathways.Conclusion:There were differentially
expressed proteins between ER/PR positive and negative breast cancer, which involved complex molecular function, biological process
and signaling pathway. |
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