Biomedical Engineering Department, Northwestern University, Evanston, Illinois, USA.
Cancer Res. 2012 Jun 1;72(11):2720-7. doi: 10.1158/0008-5472.CAN-11-3807. Epub 2012 Apr 6.
Developing a minimally invasive and cost-effective prescreening strategy for colon cancer is critical because of the impossibility of conducting colonoscopy on the entire at-risk population. The concept of field carcinogenesis, in which normal-appearing tissue away from a tumor has molecular and, consequently, nano-architectural abnormalities, offers one attractive approach to identify high-risk patients. In this study, we investigated whether the novel imaging technique partial wave spectroscopic (PWS) microscopy could risk-stratify patients harboring precancerous lesions of the colon, using an optically measured biomarker (L(d)) obtained from microscopically normal but nanoscopically altered cells. Rectal epithelial cells were examined from 146 patients, including 72 control patients, 14 patients with diminutive adenomas, 20 patients with nondiminutive/nonadvanced adenomas, 15 patients with advanced adenomas/high-grade dysplasia, 12 patients with genetic mutation leading to Lynch syndrome, and 13 patients with cancer. We found that the L(d) obtained from rectal colonocytes was well correlated with colon tumorigenicity in our patient cohort and in an independent validation set of 39 additional patients. Therefore, our findings suggest that PWS-measured L(d) is an accurate marker of field carcinogenesis. This approach provides a potential prescreening strategy for risk stratification before colonoscopy.
开发一种微创且具有成本效益的结肠癌初筛策略至关重要,因为不可能对所有高危人群进行结肠镜检查。场致癌的概念是,远离肿瘤的正常组织具有分子和纳米结构异常,这为识别高危患者提供了一种有吸引力的方法。在这项研究中,我们使用从微观上正常但纳米上改变的细胞获得的光学测量生物标志物(L(d)),研究了新型成像技术部分波谱(PWS)显微镜是否可以对患有结肠癌癌前病变的患者进行风险分层。检查了 146 名患者的直肠上皮细胞,包括 72 名对照患者、14 名小腺瘤患者、20 名非小/非晚期腺瘤患者、15 名晚期腺瘤/高级别异型增生患者、12 名遗传突变导致林奇综合征的患者和 13 名癌症患者。我们发现,从直肠结肠细胞获得的 L(d)与我们患者队列和另外 39 名患者的独立验证队列中的结肠肿瘤发生性密切相关。因此,我们的研究结果表明,PWS 测量的 L(d)是场致癌的准确标志物。这种方法为结肠镜检查前的风险分层提供了一种潜在的初筛策略。