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2D-DIGE Proteomic Analysis of Changes in Estrogen/Progesterone-Induced Rat Breast Hyperplasia upon Treatment with the Mongolian Remedy RuXian-I

机译:2D-DIGE蛋白质组学分析蒙古药如仙-I治疗后雌激素/孕酮诱发的大鼠乳腺增生的变化

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摘要

RuXian-I has traditionally been used as a remedy for breast hyperplasia in the Inner Mongolia Autonomous Region of China. As a first step toward the investigation of biomarkers associated with RuXian-I treatment, a proteome-wide analysis of rat breast tissue was conducted. First, rat breast hyperplasia was induced by injection of estradiol and progesterone. After treatment with RuXian-I, there is a marked decrease in the hyperplasia, as can be shown by decreases in the nipple diameter and the pathological changes in breast. Subsequently, we used an approach that integrates size-based 2D-DIGE, MALDI-TOF/TOF-MS, and bioinformatics to analyze data from the control group, the model group and the RuXian-I treatment group. Using this approach, seventeen affected proteins were identified. Among these, 15 (including annexin A1, annexin A2, superoxide dismutase [Mn], peroxiredoxin-1, translationally-controlled tumor protein and α B-crystallin) were significantly up-regulated in the model group and down-regulated upon treatment with RuXian-I, and two (Tpil protein and myosin-4) have the opposite change trend. The expression of annexin A1 was confirmed using immunohistochemistry. The expression of superoxide dismutase (SOD) activity was confirmed biochemically. These results indicated that RuXian-I treats rat breast hyperplasia through regulation of cell cycle, immune system, metabolic, signal transduction, etc. The differential expressions of these proteins (annexin A1, superoxide dismutase [Mn], alpha B-crystallins and translationally controlled tumor protein, among others) were associated with occurrence and metastasis of breast cancer. These findings might provide not only far-reaching valuable insights into the mechanism of RuXian-I action, but also leads for prognosis and diagnosis of breast hyperplasia and breast cancer.
机译:在中国内蒙古自治区,传统上将乳腺I用作乳腺增生的药物。作为研究与乳腺Ⅰ治疗相关的生物标志物的第一步,对大鼠乳房组织进行了蛋白质组范围的分析。首先,通过注射雌二醇和孕酮诱导大鼠乳腺增生。用乳仙I治疗后,乳头直径的减少和乳房的病理变化可以显示出增生的明显减少。随后,我们使用了一种集成基于大小的2D-DIGE,MALDI-TOF / TOF-MS和生物信息学的方法来分析来自对照组,模型组和入贤I治疗组的数据。使用这种方法,鉴定了十七种受影响的蛋白质。其中,模型组中15种(包括膜联蛋白A1,膜联蛋白A2,超氧化物歧化酶[Mn],过氧化物酶-1,翻译控制的肿瘤蛋白和αB-晶状蛋白)显着上调,而如仙治疗后下调-I和两个(Tpil蛋白和肌球蛋白-4)的变化趋势相反。使用免疫组织化学证实膜联蛋白A1的表达。生化证实超氧化物歧化酶(SOD)活性的表达。这些结果表明如仙I通过调节细胞周期,免疫系统,代谢,信号转导等来治疗大鼠乳腺增生。这些蛋白的差异表达(annexin A1,超氧化物歧化酶[Mn],αB-晶状体蛋白和翻译控制)肿瘤蛋白等)与乳腺癌的发生和转移有关。这些发现不仅可以提供对入纤Ⅰ作用机理的深远有价值的见解,而且可以为乳腺增生和乳腺癌的预后和诊断提供指导。

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