Stage-specific analysis of plasma protein profiles in ovarian cancer: Difference in-gel electrophoresis analysis of pooled clinical samples.

Q1 Environmental Science
Journal of Carcinogenesis Pub Date : 2013-06-29 Print Date: 2013-01-01 DOI:10.4103/1477-3163.114216
Mark J Bailey, Kristy L Shield-Artin, Karen Oliva, Mustafa Ayhan, Simone Reisman, Gregory E Rice
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引用次数: 14

Abstract

Introduction: Ovarian cancer is the leading cause of death from gynecological cancer. Non-specific symptoms early in disease and the lack of specific biomarkers hinder early diagnosis. Multi-marker blood screening tests have shown promise for improving identification of early stage disease; however, available tests lack sensitivity, and specificity.

Materials and methods: In this study, pooled deeply-depleted plasma from women with Stage 1, 2 or 3 ovarian cancer and healthy controls were used to compare the 2-dimensional gel electrophoresis (2-DE) protein profiles and identify potential novel markers of ovarian cancer progression.

Results/discussion: Stage-specific variation in biomarker expression was observed. For example, apolipoprotein A1 expression is relatively low in control and Stage 1, but shows a substantial increase in Stage 2 and 3, thus, potential of utility for disease confirmation rather than early detection. A better marker for early stage disease was tropomyosin 4 (TPM4). The expression of TPM4 increased by 2-fold in Stage 2 before returning to "normal" levels in Stage 3 disease. Multiple isoforms were also identified for some proteins and in some cases, displayed stage-specific expression. An interesting example was fibrinogen alpha, for which 8 isoforms were identified. Four displayed a moderate increase at Stage 1 and a substantial increase for Stages 2 and 3 while the other 4 showed only moderate increases.

Conclusion: Herein is provided an improved summary of blood protein profiles for women with ovarian cancer stratified by stage.

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卵巢癌血浆蛋白谱的分期特异性分析:汇集临床样本的凝胶电泳分析差异
卵巢癌是导致妇科癌症死亡的主要原因。疾病早期的非特异性症状和缺乏特异性生物标志物阻碍了早期诊断。多标记物血液筛查试验已显示出改善早期疾病识别的希望;然而,现有的检测缺乏敏感性和特异性。材料和方法:在本研究中,收集了来自1期、2期或3期卵巢癌妇女和健康对照者的深度耗尽血浆,用于比较二维凝胶电泳(2- de)蛋白谱,并确定卵巢癌进展的潜在新标志物。结果/讨论:观察到生物标志物表达的阶段性变化。例如,载脂蛋白A1在对照组和第一阶段的表达相对较低,但在第二和第三阶段显示出大量增加,因此,在疾病确认而不是早期发现方面具有潜在的效用。较好的早期疾病标志物是原肌球蛋白4 (TPM4)。TPM4的表达在2期增加了2倍,然后在3期疾病中恢复到“正常”水平。一些蛋白质的多个同种异构体也被鉴定出来,在某些情况下,显示出特定阶段的表达。一个有趣的例子是纤维蛋白原α,鉴定出8种同种异构体。其中4人在第一阶段表现出中度增加,在第二和第三阶段大幅增加,而其他4人仅表现出中度增加。结论:本文提供了一个改进的总结血蛋白谱的妇女卵巢癌分期分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Carcinogenesis
Journal of Carcinogenesis Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
7.50
自引率
0.00%
发文量
0
审稿时长
15 weeks
期刊介绍: Journal of Carcinogenesis considers manuscripts in many areas of carcinogenesis and Chemoprevention. Primary areas of interest to the journal include: physical and chemical carcinogenesis and mutagenesis; processes influencing or modulating carcinogenesis, such as DNA repair; genetics, nutrition, and metabolism of carcinogens; the mechanism of action of carcinogens and modulating agents; epidemiological studies; and, the formation, detection, identification, and quantification of environmental carcinogens. Manuscripts that contribute to the understanding of cancer prevention are especially encouraged for submission
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