Biosciences Core Laboratories, Research Department, King Abdullah University of Science and Technology Thuwal, Kingdom of Saudi Arabia.
Front Genet. 2014 Aug 27;5:182. doi: 10.3389/fgene.2014.00182. eCollection 2014.
Cell-free nucleic acids (CFNA) have been reported by several authors in blood, stool, and urine of patients with colorectal cancer (CRC). These genetic biomarkers can be an indication of neoplastic colorectal epithelial cells, and can thus potentially be used as noninvasive tests for the detection of the disease in CRC patients and monitor their staging, without the need to use heavier and invasive tools. In a number of test-trials, these genetic tests have shown the advantage of non-invasiveness, making them well accepted by most of the patients, without major side effects. They have also shown a promising sensitivity and specificity in the detection of malignant and premalignant neoplasms. Moreover, costs for performing such tests are very low. Several studies reported and confirmed the proof of the principle for these genetic tests for screening, diagnosis, and prognosis; the main challenge of translating this approach from research to clinical laboratory is the validation from large and long-term randomized trials to prove sustainable high sensitivity and specificity. In this paper, we present a review on the noninvasive genetics biomarkers for CRC detection described in the literature and the challenges that can be encountered for validation processes.
无细胞核酸 (CFNA) 已被多位作者在结直肠癌 (CRC) 患者的血液、粪便和尿液中报道。这些遗传生物标志物可以作为肿瘤性结直肠上皮细胞的指标,因此可以潜在地用作 CRC 患者疾病的非侵入性检测手段,并监测其分期,而无需使用更重和侵入性的工具。在许多试验中,这些遗传测试显示了非侵入性的优势,因此得到了大多数患者的认可,且没有主要的副作用。它们在检测恶性和癌前肿瘤方面也显示出了有前途的敏感性和特异性。此外,执行此类测试的成本非常低。多项研究报告并证实了这些遗传测试在筛查、诊断和预后方面的原理证据;将这种方法从研究转化为临床实验室的主要挑战是通过大样本和长期随机试验来验证其可持续的高敏感性和特异性。在本文中,我们对文献中描述的用于 CRC 检测的非侵入性遗传生物标志物以及验证过程中可能遇到的挑战进行了综述。