Cancer Biology and Infectious Disease Research Center, Eastern Virginia Medical School, Norfolk, Virginia 23507, USA.
OMICS. 2011 May;15(5):251-9. doi: 10.1089/omi.2010.0120. Epub 2011 Feb 19.
Over the past decade, multiple genetic and histological approaches have accelerated development of new breast cancer diagnostics and treatment paradigms. Multiple distinct genetic subtypes of breast cancers have been defined, and this has progressively led toward more personalized medicine in regard to treatment options. There still remains a deficiency in the development of molecular diagnostic assays that can be used for breast cancer detection and pretherapy clinical decisions. In particular, the type of cancer-specific biomarker typified by a serum or tissue-derived protein. Progress in this regard has been minimal, especially in comparison to the rapid advancements in genetic and histological assays for breast cancers. In this review, some potential reasons for this large gap in developing protein biomarkers will be discussed, as well as new strategies for improving these approaches. Improvements in the study design of protein biomarker discovery strategies in relation to the genetic subtypes and histology of breast cancers is also emphasized. The current successes in use of genetic and histological assays for breast cancer diagnostics are summarized, and in that context, the current limitations of the types of breast cancer-related clinical samples available for protein biomarker assay development are discussed. Based on these limitations, research strategies emphasizing identification of glycoprotein biomarkers in blood and MALDI mass spectrometry imaging of tissues are described.
在过去的十年中,多种遗传和组织学方法加速了新的乳腺癌诊断和治疗模式的发展。已经定义了多种不同的乳腺癌遗传亚型,这逐渐导致了针对治疗选择的更个性化的医学。在用于乳腺癌检测和治疗前临床决策的分子诊断检测方面仍然存在不足。特别是在癌症特异性生物标志物方面,其典型代表是血清或组织来源的蛋白质。在这方面的进展微乎其微,尤其是与乳腺癌的遗传和组织学检测的快速进展相比。在这篇综述中,将讨论在开发蛋白质生物标志物方面存在这种巨大差距的一些潜在原因,以及改进这些方法的新策略。还强调了与乳腺癌的遗传亚型和组织学相关的蛋白质生物标志物发现策略的研究设计的改进。总结了目前在使用遗传和组织学检测进行乳腺癌诊断方面的成功经验,并在此背景下讨论了当前用于蛋白质生物标志物检测开发的乳腺癌相关临床样本类型的局限性。基于这些局限性,描述了强调鉴定血液中糖蛋白生物标志物和组织 MALDI 质谱成像的研究策略。