Department of Medical Oncology, OncoProteomics Laboratory, VU University Medical Center, Amsterdam, the Netherlands.
Clin Biochem. 2013 Apr;46(6):466-79. doi: 10.1016/j.clinbiochem.2012.10.039. Epub 2012 Nov 13.
Colorectal cancer (CRC) is a major cause of cancer-related death in the western world. Screening to detect the disease in an early stage is the most effective approach to tackle this problem. In addition, better diagnostic tools for assessment of prognosis and prediction of response to drug therapy will allow for personalized therapies and better outcomes. Protein biomarkers that reflect tumor biology have the potential to address a wide range of clinical needs. These include diagnostic (screening) biomarkers for early detection, prognostic biomarkers for estimation of disease outcome, predictive biomarkers for adjuvant treatment stratification, and surveillance biomarkers for disease monitoring and treatment response. An important source for the discovery of potential biomarkers comes from mass spectrometry based proteomics research of the biology of CRC development. Here, we review recent colon cancer proteomics studies directed at identification of biomarker proteins. These include studies that use preclinical models (i.e. cell lines or murine tissues) as well as clinical materials (e.g. tissue and stool samples). We separately highlight some studies that focused on identification of cancer stem cell (CSC) related proteins in tumor spheroids, an in vitro model system for investigating CRC treatment response. Recent proteomics studies have generated many new candidate protein biomarkers. However, the lack of follow-up studies that lead to biomarker verification and/or validation remains a limiting factor in the translation of these candidate biomarkers into clinical applications. This is partly due to technological limitations which are bound to diminish with new technologies, including selected reaction monitoring mass spectrometry (SRM-MS). Antibodies are still required, though, both to perform high-throughput validation as well as to develop cost-effective tests for routine use in a clinical setting.
结直肠癌(CRC)是西方世界癌症相关死亡的主要原因。通过筛查在早期发现疾病是解决这个问题的最有效方法。此外,更好的诊断工具用于评估预后和预测药物治疗反应将允许个性化治疗和更好的结果。反映肿瘤生物学的蛋白质生物标志物有可能满足广泛的临床需求。这些包括用于早期检测的诊断(筛选)生物标志物、用于估计疾病结果的预后生物标志物、用于辅助治疗分层的预测生物标志物以及用于疾病监测和治疗反应的监测生物标志物。发现潜在生物标志物的一个重要来源是基于 CRC 发展生物学的质谱蛋白质组学研究。在这里,我们回顾了最近针对生物标志物蛋白鉴定的结肠癌蛋白质组学研究。这些研究包括使用临床前模型(即细胞系或鼠组织)和临床材料(例如组织和粪便样本)的研究。我们分别强调了一些研究,这些研究集中在鉴定肿瘤球体中的癌症干细胞(CSC)相关蛋白,肿瘤球体是一种用于研究 CRC 治疗反应的体外模型系统。最近的蛋白质组学研究产生了许多新的候选蛋白生物标志物。然而,缺乏导致生物标志物验证和/或验证的后续研究仍然是将这些候选生物标志物转化为临床应用的一个限制因素。这部分是由于技术限制,这些限制随着新技术的出现,包括选择反应监测质谱(SRM-MS),必然会减少。仍然需要抗体,既需要进行高通量验证,也需要开发用于临床常规使用的具有成本效益的测试。