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Proteomic Profiling of Inherited Breast Cancer: Identification of Molecular Targets for Early Detection, Prognosis and Treatment, and Related Bioinformatics Tools

机译:遗传乳腺癌蛋白质组学分析:鉴定早期检测,预后和治疗和相关生物信息学工具的分子靶标

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Proteomic-based approaches are quickly becoming a powerful and widely used technique to identify specific "molecular signatures" in several pathologic conditions. In particular, cancer, which is one of the most challenging and socially important diseases, is currently under intensive investigation in order to overcome limitations still affecting conventional diagnostic strategies. In particular, one of the major goals in this field is the identification of reliable markers for early diagnosis, as well as for prognosis and treatment. Among cancer, breast carcinoma is the most important malignant disease for western women. A hereditary form has been identified which is related to inherited cancer-predisposing germ-line mutations. Germ-line mutations of BRCA1 gene have been identified in 15-20% of women with a family history of breast cancer and 60-80% with family history of both breast and ovarian cancer. Pathological as well as molecular profiling studies support the concept that inherited breast tumors are different forms of disease, suggesting the intriguing possibility of tailored chemopreventive and therapeutic approaches in this setting. Bioinformatics, and in particular pattern recognition learning algorithms, offer the enabling analysis tools, so the paper also discusses a software environment to conduct such data-intensive computations over Computational Grids.
机译:基于蛋白质组学的方法迅速成为一种强大而广泛使用的技术,以识别若干病理条件中的特定“分子签发”。特别是,癌症是最具挑战性和社会重要性的疾病之一,目前正在密集调查中,以克服仍然影响常规诊断策略的局限性。特别是,该领域的主要目标之一是鉴定早期诊断的可靠标志物,以及预后和治疗。在癌症中,乳腺癌是西方女性最重要的恶性疾病。已经鉴定了一种遗传形式,其与遗传癌症易感性突变有关。 BRCA1基因的生细胞突变已在15-20%的患有乳腺癌家族史和60-80%的女性中鉴定出乳腺癌和卵巢癌的家族史。病理以及分子剖面研究支持遗传患乳腺肿瘤的概念是不同形式的疾病,这表明在该环境中定制了化学预防和治疗方法的兴趣可能性。生物信息学,特别是模式识别学习算法,提供了启用分析工具,因此本文还讨论了在计算网格上进行此类数据密集型计算的软件环境。

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