结直肠癌细胞凋亡通路的预后价值:免疫组织化学鉴定的生物标志物文献综述

Eliane C M Zeestraten, Anne Benard, Marlies S Reimers, Philip C Schouten, Gerrit J Liefers, Cornelis J H van de Velde, Peter J K Kuppen
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引用次数: 73

摘要

预测结直肠癌(CRC)患者预后的生物标志物研究正在迅速扩大。然而,这些生物标志物都没有被美国临床肿瘤协会或欧洲肿瘤标志物组织推荐使用。目前的分期标准导致大量CRC患者治疗不足或过度。逃避细胞凋亡是肿瘤发生的一个特征,已知与患者预后相关。我们回顾了1998年至2011年间基于免疫组织化学的研究文献,这些研究描述了CRC中这一途径的生物标志物,并确定了26个标志物。最常见的描述是p53、Bcl-2、survivin、Fas和TRAILR1受体及其配体。所回顾的研究中没有一项为在当前临床实践中实施单一标记物提供足够的支持。这可能是由于这一途径的复杂生物学特性。我们建议将重点放在细胞凋亡通路内的关键标记物的组合上,这些标记物共同代表了“凋亡肿瘤谱”,从而更好地反映了该通路在肿瘤中的地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The prognostic value of the apoptosis pathway in colorectal cancer: a review of the literature on biomarkers identified by immunohistochemistry.

The prognostic value of the apoptosis pathway in colorectal cancer: a review of the literature on biomarkers identified by immunohistochemistry.

Research towards biomarkers that predict patient outcome in colorectal cancer (CRC) is rapidly expanding. However, none of these biomarkers have been recommended by the American Association of Clinical Oncology or the European Group on Tumor Markers. Current staging criteria result in substantial under-and over-treatment of CRC patients. Evasion of apoptosis, a characteristic feature of tumorigenesis, is known to correlate with patient outcome. We reviewed the literature on immunohistochemistry-based studies between 1998 and 2011 describing biomarkers in this pathway in CRC and identified 26 markers. Most frequently described were p53, Bcl-2, survivin, and the Fas and TRAILR1 receptors and their ligands. None of the studies reviewed provided sufficient support for implementing a single marker into current clinical practice. This is likely due to the complex biology of this pathway. We suggest focusing on the combination of key markers within the apoptosis pathway that together represent an 'apoptotic tumor profile', which better reflects the status of this pathway in a tumor.

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