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本文引用的文献

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J Pathol. 2012 Jun;227(2):223-33. doi: 10.1002/path.3986. Epub 2012 Feb 17.
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Sorafenib-induced mitochondrial complex I inactivation and cell death in human neuroblastoma cells.索拉非尼诱导人神经母细胞瘤细胞线粒体复合物 I 失活和细胞死亡。
J Proteome Res. 2012 Mar 2;11(3):1609-20. doi: 10.1021/pr200790e. Epub 2012 Feb 15.
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Cancer statistics, 2012.癌症统计数据,2012 年。
CA Cancer J Clin. 2012 Jan-Feb;62(1):10-29. doi: 10.3322/caac.20138. Epub 2012 Jan 4.
4
Tumor classification of six common cancer types based on proteomic profiling by MALDI imaging.基于 MALDI 成像的蛋白质组特征分析对六种常见癌症类型的肿瘤分类。
J Proteome Res. 2012 Mar 2;11(3):1996-2003. doi: 10.1021/pr200784p. Epub 2012 Feb 3.
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Protein significance analysis in selected reaction monitoring (SRM) measurements.选择反应监测(SRM)测量中的蛋白质意义分析。
Mol Cell Proteomics. 2012 Apr;11(4):M111.014662. doi: 10.1074/mcp.M111.014662. Epub 2011 Dec 21.
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Clinical proteomics identified ATP-dependent RNA helicase DDX39 as a novel biomarker to predict poor prognosis of patients with gastrointestinal stromal tumor.临床蛋白质组学鉴定 ATP 依赖的 RNA 解旋酶 DDX39 作为预测胃肠道间质瘤患者不良预后的新型生物标志物。
J Proteomics. 2012 Feb 2;75(4):1089-98. doi: 10.1016/j.jprot.2011.10.005. Epub 2011 Oct 25.
7
Repercussion of Mitochondria Deformity Induced by Anti-Hsp90 Drug 17AAG in Human Tumor Cells.抗Hsp90药物17AAG诱导的线粒体畸形对人肿瘤细胞的影响
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Proteomic study of malignant pleural mesothelioma by laser microdissection and two-dimensional difference gel electrophoresis identified cathepsin D as a novel candidate for a differential diagnosis biomarker.激光显微切割和二维差异凝胶电泳的恶性胸膜间皮瘤蛋白质组学研究鉴定组织蛋白酶 D 为一种新的鉴别诊断生物标志物候选物。
J Proteomics. 2012 Jan 4;75(3):833-44. doi: 10.1016/j.jprot.2011.09.026. Epub 2011 Oct 5.
9
Proteomics-based identification of spontaneous regression-associated proteins in neuroblastoma.基于蛋白质组学的神经母细胞瘤自发消退相关蛋白的鉴定。
J Pediatr Surg. 2011 Oct;46(10):1948-55. doi: 10.1016/j.jpedsurg.2011.06.024.
10
Comparison of humoral immune responses to Epstein-Barr virus and Kaposi's sarcoma-associated herpesvirus using a viral proteome microarray.采用病毒蛋白质组微阵列比较针对 Epstein-Barr 病毒和卡波西肉瘤相关疱疹病毒的体液免疫反应。
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蛋白质组学在软组织肉瘤中的应用。

Application of proteomics to soft tissue sarcomas.

作者信息

Kondo Tadashi, Kubota Daisuke, Kawai Akira

机构信息

Division of Pharmacoproteomics, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.

出版信息

Int J Proteomics. 2012;2012:876401. doi: 10.1155/2012/876401. Epub 2012 Jun 19.

DOI:10.1155/2012/876401
PMID:22778956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3388341/
Abstract

Soft tissue sarcomas are rare and account for less than 1% of all malignant cancers. Other than development of intensive therapies, the clinical outcome of patients with soft tissue sarcoma remains very poor, particularly when diagnosed at a late stage. Unique mutations have been associated with certain soft tissue sarcomas, but their etiologies remain unknown. The proteome is a functional translation of a genome, which directly regulates the malignant features of tumors. Thus, proteomics is a promising approach for investigating soft tissue sarcomas. Various proteomic approaches and clinical materials have been used to address clinical and biological issues, including biomarker development, molecular target identification, and study of disease mechanisms. Several cancer-associated proteins have been identified using conventional technologies such as 2D-PAGE, mass spectrometry, and array technology. The functional backgrounds of proteins identified were assessed extensively using in vitro experiments, thus supporting expression analysis. These observations demonstrate the applicability of proteomics to soft tissue sarcoma studies. However, the sample size in each study was insufficient to allow conclusive results. Given the low frequency of soft tissue sarcomas, multi-institutional collaborations are required to validate the results of proteomic approaches.

摘要

软组织肉瘤较为罕见,在所有恶性肿瘤中所占比例不到1%。除了强化治疗的发展外,软组织肉瘤患者的临床结局仍然很差,尤其是在晚期被诊断出来时。独特的突变与某些软组织肉瘤有关,但其病因仍不清楚。蛋白质组是基因组的功能性翻译产物,直接调控肿瘤的恶性特征。因此,蛋白质组学是研究软组织肉瘤的一种很有前景的方法。各种蛋白质组学方法和临床材料已被用于解决临床和生物学问题,包括生物标志物开发、分子靶点鉴定和疾病机制研究。使用二维聚丙烯酰胺凝胶电泳、质谱分析和阵列技术等传统技术已鉴定出几种与癌症相关的蛋白质。通过体外实验广泛评估了所鉴定蛋白质的功能背景情况从而支持表达分析。这些观察结果证明了蛋白质组学在软组织肉瘤研究中的适用性。然而,每项研究中的样本量都不足以得出确凿的结果。鉴于软组织肉瘤的发病率较低,需要多机构合作来验证蛋白质组学方法的结果。