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用于不同淋巴结状态乳腺癌预后的候选血浆生物标志物的无标记定量蛋白质组学筛查

Label-Free Quantitative Proteomic Screening of Candidate Plasma Biomarkers for the Prognosis of Breast Cancer with Different Lymph Node Statuses.

作者信息

Chen Ling, Zhao Weibo, He Jing, Li Liqi, Meng Dong, Cai Dongyan, Yu Jinjin, Chen Daozhen, Wu Yibo, Zhou Tao

机构信息

Department of Breast Surgery, Affiliated Hospital of Jiangnan University, Wuxi, P. R. China.

Laboratory of Genomic and Precision Medicine, Jiangnan University, Wuxi, P. R. China.

出版信息

Proteomics Clin Appl. 2018 May;12(3):e1700117. doi: 10.1002/prca.201700117. Epub 2018 Feb 14.

Abstract

PURPOSE

Lymph node status is a crucial predictor for the overall survival of invasive breast cancer. However, lymph node involvement is only detected in about half of HER2-positive patients. Since patients with lymph node involvement has less favorable prognosis and higher risk of recurrence, it is important to develop plasma protein biomarkers for distinguishing lymph node metastasis.

EXPERIMENTAL DESIGN

A label-free quantitative proteomic strategy to construct plasma proteomes of ten patients with small size HER2-positive breast cancer (five patients with lymph node metastasis versus five patients without lymph node metastasis) is applied.

RESULTS

A total of 388 proteins are identified, of which 33 proteins are differentially expressed. Statistical analyses suggested the present strategy is low cost and highly efficient in initial screening of plasma biomarkers. In silico analyses using various bioinformatics databases show that these altered proteins are highly associated with breast disease, cancer pathway, lymph node morphology, metastasis, complement pathway, and immune regulation.

CONCLUSIONS AND CLINICAL RELEVANCE

The present dataset provides a list of candidate biomarkers that could be used for early differentiation diagnosis and prognosis of breast cancer with lymph node metastasis.

摘要

目的

淋巴结状态是浸润性乳腺癌总体生存的关键预测指标。然而,仅约一半的HER2阳性患者会检测到淋巴结受累。由于淋巴结受累的患者预后较差且复发风险较高,因此开发用于区分淋巴结转移的血浆蛋白生物标志物非常重要。

实验设计

应用一种无标记定量蛋白质组学策略构建10例小尺寸HER2阳性乳腺癌患者(5例有淋巴结转移,5例无淋巴结转移)的血浆蛋白质组。

结果

共鉴定出388种蛋白质,其中33种蛋白质差异表达。统计分析表明,本策略在血浆生物标志物的初步筛选中成本低且效率高。使用各种生物信息学数据库进行的计算机分析表明,这些改变的蛋白质与乳腺疾病、癌症通路、淋巴结形态、转移、补体通路和免疫调节高度相关。

结论及临床意义

本数据集提供了一份候选生物标志物清单可用于伴淋巴结转移乳腺癌的早期鉴别诊断和预后评估。

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