Stevens Richard G, Swede Helen, Rosenberg Daniel W
Colon Cancer Prevention Program (CCPP), Neag Comprehensive Cancer Center, University of Connecticut Health Center (UCHC), 263 Farmington Avenue, Farmington, CT 06030-6325, United States.
Cancer Lett. 2007 Jul 18;252(2):171-83. doi: 10.1016/j.canlet.2006.11.009. Epub 2006 Dec 19.
Since first described in a rodent model in 1987, aberrant crypt foci (ACF) in the colon have been shown to exhibit many of the molecular features of the more advanced colonic neoplasms including cancer. Therefore, they may be early lesions with potential for progression, and be valuable biomarkers for reduction of risk of colorectal cancer (CRC). For this review, we searched PubMed, and reference lists of recent publications, for studies which reported on associations of features of ACF in humans, such as number or size, with subject characteristics, such as age or family history of CRC. Over 150 papers have reported on ACF in humans. However, the vast majority of these publications are concerned with molecular and morphological features of biopsied lesions, and not their epidemiology. None of the epidemiological studies were of optimum design, primarily due to their absence of a well-defined subject sampling frame or method. Given their 'first-generation' nature, consistent findings were of increased ACF number with age and with synchronous advanced colonic neoplasia. One study reported a higher mean number of ACF in subjects with a family history of CRC than in those without. The strongest evidence on the ability of ACF to predict a diagnosis of CRC will be from prospective studies with baseline ACF assessment in a large sample of disease-free persons (many thousands) who are followed carefully for many years. In the interim, because ACF are asymptomatic, well-designed cross-sectional studies are feasible and will yield valuable information on the relation of ACF to the known risk factors for CRC. This information can then be used to improve the design of prospective studies, and of clinical intervention trials that use ACF as an intermediate endpoint.
自1987年在啮齿动物模型中首次被描述以来,结肠中的异常隐窝灶(ACF)已被证明具有包括癌症在内的更晚期结肠肿瘤的许多分子特征。因此,它们可能是具有进展潜力的早期病变,并且是降低结直肠癌(CRC)风险的有价值的生物标志物。在本次综述中,我们在PubMed以及近期出版物的参考文献列表中搜索了有关人类ACF特征(如数量或大小)与受试者特征(如年龄或CRC家族史)之间关联的研究。已有150多篇论文报道了人类ACF的情况。然而,这些出版物绝大多数关注的是活检病变的分子和形态特征,而非其流行病学。没有一项流行病学研究设计得尽善尽美,主要原因是缺乏明确的受试者抽样框架或方法。鉴于其“第一代”的性质,一致的研究结果是ACF数量随年龄增长以及与同步发生的晚期结肠肿瘤增加。一项研究报告称,有CRC家族史的受试者中ACF的平均数量高于无家族史者。关于ACF预测CRC诊断能力的最有力证据将来自对大量(数千名)无病个体进行基线ACF评估并进行多年仔细随访的前瞻性研究。在此期间,由于ACF无症状,设计良好的横断面研究是可行的,并且将产生关于ACF与CRC已知风险因素之间关系的有价值信息。然后,这些信息可用于改进前瞻性研究以及将ACF用作中间终点的临床干预试验的设计。