Gonzalez-Pons Maria, Cruz-Correa Marcia
Department of Gastrointestinal Oncology and Genetics, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR 00927-6346, USA ; UPR-MDACC Partnership for Excellence in Cancer Research Program, University of Puerto Rico Medical Sciences Campus, San Juan, PR 00936-5067, USA.
Department of Gastrointestinal Oncology and Genetics, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR 00927-6346, USA ; UPR-MDACC Partnership for Excellence in Cancer Research Program, University of Puerto Rico Medical Sciences Campus, San Juan, PR 00936-5067, USA ; Department of Medicine, Biochemistry, and Surgery, University of Puerto Rico School of Medicine, San Juan, PR 00936-5067, USA.
Biomed Res Int. 2015;2015:149014. doi: 10.1155/2015/149014. Epub 2015 May 27.
Colorectal cancer is one of the major causes of cancer-related death in the Western world. Patient survival is highly dependent on the tumor stage at the time of diagnosis. Reduced sensitivity to chemotherapy is still a major obstacle in effective treatment of advanced disease. Due to the fact that colorectal cancer is mostly asymptomatic until it progresses to advanced stages, the implementation of screening programs aimed at early detection is essential to reduce incidence and mortality rates. Current screening and diagnostic methods range from semi-invasive procedures such as colonoscopy to noninvasive stool-based tests. The combination of the absence of symptoms, the semi-invasive nature of currently used methods, and the suboptimal accuracy of fecal blood tests results in colorectal cancer diagnosis at advanced stages in a significant number of individuals. Alterations in gene expression leading to colorectal carcinogenesis are reflected in dysregulated levels of nucleic acids and proteins, which can be used for the development of novel, minimally invasive molecular biomarkers. The purpose of this review is to discuss the commercially available colorectal cancer molecular diagnostic methods as well as to highlight some of the new candidate predictive and prognostic molecular markers for tumor, stool, and blood samples.
在西方世界,结直肠癌是癌症相关死亡的主要原因之一。患者的生存率高度依赖于诊断时的肿瘤分期。对化疗敏感性降低仍然是晚期疾病有效治疗的主要障碍。由于结直肠癌在进展到晚期之前大多没有症状,实施旨在早期检测的筛查计划对于降低发病率和死亡率至关重要。当前的筛查和诊断方法从结肠镜检查等半侵入性程序到基于粪便的非侵入性检测不等。无症状、当前使用方法的半侵入性性质以及粪便潜血检测的准确性欠佳,导致大量个体在晚期才被诊断出患有结直肠癌。导致结直肠癌发生的基因表达改变反映在核酸和蛋白质水平的失调上,这可用于开发新型的、微创分子生物标志物。本综述的目的是讨论市售的结直肠癌分子诊断方法,并突出一些用于肿瘤、粪便和血液样本的新的候选预测和预后分子标志物。