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采用差异分泌组学方法鉴定结直肠癌转移的血清生物标志物。

Identification of serum biomarkers for colorectal cancer metastasis using a differential secretome approach.

机构信息

Department of Pathology & Pathophysiology, Affiliated Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

出版信息

J Proteome Res. 2010 Jan;9(1):545-55. doi: 10.1021/pr9008817.

Abstract

Lymph node metastasis is the major concern that causes death in colorectal cancers. However, biomarkers for cancer metastasis are still lacking. In this study, we applied an LC-MS/MS-based label-free quantitative proteomics approach to compare the differential secretome of a primary cell line SW480 and its lymph node metastatic cell line SW620 from the same colorectal cancer patient. We identified a total of 910 proteins from the conditioned media and 145 differential proteins between SW480 and SW620 (>1.5-fold change). The differential expression pattern of 6 candidate proteins was validated by Western blot analysis. Among them, trefoil factor 3 and growth/differentiation factor 15, two up-regulated proteins in SW620, were further analyzed in a large cohort of clinical tissue and serum samples. Sandwich ELISA assay showed that the serum levels of both proteins were significantly higher in lymph node metastatic colorectal cancers. Receiver operating characteristic curve analysis confirmed that serum trefoil factor 3 and growth/differentiation factor 15 could provide a discriminatory diagnostic test for predicting colorectal cancer metastasis. Immunohistochemical analysis also showed that the overexpression of trefoil factor 3 or growth/differentiation factor 15 in colorectal cancer was associated with lymph node metastatic behavior. This study showed an accurate, sensitive, and robust label-free quantitation approach for differential analysis of cancer secretome. The comparison of the cancer secretome in vitro is a feasible strategy to obtain valuable biomarkers for potential clinical application. Both trefoil factor 3 and growth/differentiation factor 15 could serve as potential biomarkers for the prediction of colorectal cancer metastasis.

摘要

淋巴结转移是导致结直肠癌患者死亡的主要关注点。然而,癌症转移的生物标志物仍然缺乏。在这项研究中,我们应用基于 LC-MS/MS 的无标记定量蛋白质组学方法比较了来自同一结直肠癌患者的原发性细胞系 SW480 和其淋巴结转移细胞系 SW620 的差异分泌组。我们从条件培养基中鉴定出了总共 910 种蛋白质和 SW480 与 SW620 之间的 145 种差异蛋白质 (>1.5 倍变化)。通过 Western blot 分析验证了 6 种候选蛋白的差异表达模式。其中,在 SW620 中上调的两种蛋白三叶因子 3 和生长/分化因子 15 的表达模式通过进一步在大量临床组织和血清样本中进行分析。夹心 ELISA 检测表明,淋巴结转移结直肠癌患者血清中这两种蛋白的水平明显升高。接受者操作特征曲线分析证实,血清三叶因子 3 和生长/分化因子 15 可提供用于预测结直肠癌转移的鉴别诊断测试。免疫组织化学分析还表明,三叶因子 3 或生长/分化因子 15 在结直肠癌中的过表达与淋巴结转移行为相关。本研究显示了一种准确、敏感、稳健的无标记定量分析癌症分泌组的方法。体外比较癌症分泌组是获得潜在临床应用有价值生物标志物的可行策略。三叶因子 3 和生长/分化因子 15 均可作为预测结直肠癌转移的潜在生物标志物。

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