Research of New Biomarker for Breast Cancer Using Proteomic Patterns

Y. Jung, Ho-Seung Kim, T. Yoon, M. Jeon, Y. Yoon, Y. Lee, Kitty Lee, Hyelim Kim, M. Kim, H. Park
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Abstract

Purpose: Early detection and treatment of cancer is a primary focus of health care. Many serum markers are available for breast cancer, but are not good enough for screening. Cancer antigen CA 15-3 is the most widely used biomarker for breast cancer. However, CA 15-3 has low sensitivity and specificity. This study was performed to analyze the serum proteomic pattern in breast cancer patients by surface-enhanced laser desoption/ionization timeof-flight (SELDI-TOF). Methods: We screened for potential tumor biomarkers in 42 serum samples, including samples from a group of 23 breast cancer patients at different clinical stages [stage I (n=3), stage II (n=11), stage III (n=6), and stage IV (n=1)], and a control group of 19 healthy women. Diluted serum samples were applied to a C16 hydrophobic interaction chip (H4). Complex protein profiles of different groups were compared and analyzed using the Protein Chip software 2.1 (Ciphergen Biosystems). Results: There were 7 significant protein peaks in the breast cancer group and 5 in the control group. Scoring the expression of each peak, the mean score was 8.5 in the cancer group and 3.5 in the control. The results of the combination of each peak were highly sensitive (91.2%) and specific (94.7%). These proteomic patterns did not correlate with tumor stage and hormonal receptor, c-erb B2. Conclusion: In this preliminary report, we identified protein profiles that were differentiated in breast cancer patients. After proper validation, serum proteomic pattern analysis may ultimately be applied in screening breast cancer as a stand-alone or combined with current options. (Journal of Korean Breast Cancer Society 2004;7:22-26) ꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏ
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利用蛋白质组学模式研究乳腺癌新的生物标志物
目的:早期发现和治疗癌症是医疗保健的首要重点。许多血清标记物可用于乳腺癌,但不足以用于筛查。癌抗原ca15 -3是应用最广泛的乳腺癌生物标志物。但CA 15-3的敏感性和特异性较低。本研究采用表面增强激光脱选/电离飞行时间(SELDI-TOF)分析乳腺癌患者血清蛋白质组学模式。方法:在42份血清样本中筛选潜在的肿瘤生物标志物,包括23名不同临床分期的乳腺癌患者[I期(n=3)、II期(n=11)、III期(n=6)和IV期(n=1)],以及19名健康女性的对照组。稀释后的血清样品应用于C16疏水相互作用芯片(H4)。采用protein Chip软件2.1 (Ciphergen Biosystems)对不同组的复杂蛋白谱进行比较分析。结果:乳腺癌组有7个显著蛋白峰,对照组有5个显著蛋白峰。对每个峰的表达进行评分,癌症组的平均得分为8.5,对照组的平均得分为3.5。各峰组合结果敏感性高(91.2%),特异性高(94.7%)。这些蛋白质组学模式与肿瘤分期和激素受体c- erbb B2无关。结论:在这份初步报告中,我们确定了乳腺癌患者中分化的蛋白谱。经过适当的验证后,血清蛋白质组学模式分析可能最终作为一种单独的或与当前选择相结合的方法应用于乳腺癌筛查。(韩国乳腺癌社会杂志2004;7:22-26)ꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏ
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