Pal Rahul, Shilagard Tuya, Yang Jinping, Villarreal Paula, Brown Tyra, Qiu Suimin, McCammon Susan, Resto Vicente, Vargas Gracie
Center for Biomedical Engineering, The University of Texas Medical Branch, Galveston, Texas. Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, Texas.
Center for Biomedical Engineering, The University of Texas Medical Branch, Galveston, Texas.
Cancer Res. 2016 Aug 15;76(16):4637-47. doi: 10.1158/0008-5472.CAN-16-0252. Epub 2016 Jun 14.
Early neoplastic features in oral epithelial dysplasia are first evident at the basal epithelium positioned at the epithelial-connective tissue interface (ECTI), separating the basal epithelium from the underlying lamina propria. The ECTI undergoes significant deformation in early neoplasia due to focal epithelial expansion and proteolytic remodeling of the lamina propria, but few studies have examined these changes. In the present study, we quantitated alterations in ECTI topography in dysplasia using in vivo volumetric multiphoton autofluorescence microscopy and second harmonic generation microscopy. The label-free method allows direct noninvasive visualization of the ECTI surface without perturbing the epithelium. An image-based parameter, "ECTI contour," is described that indicates deformation of the ECTI surface. ECTI contour was higher in dysplasia than control or inflamed specimens, indicating transition from flat to a deformed surface. Cellular parameters of nuclear area, nuclear density, coefficient of variation in nuclear area in the basal epithelium and collagen density in areas adjacent to ECTI were measured. ECTI contour differentiated dysplasia from control/benign mucosa with higher sensitivity and specificity than basal nuclear density or basal nuclear area, comparable with coefficient of variation in nuclear area and collagen density. The presented method offers a unique opportunity to study ECTI in intact mucosa with simultaneous assessment of cellular and extracellular matrix features, expanding opportunities for studies of early neoplastic events near this critical interface and potentially leading to development of new approaches for detecting neoplasia in vivo Cancer Res; 76(16); 4637-47. ©2016 AACR.
口腔上皮发育异常的早期肿瘤特征首先在位于上皮-结缔组织界面(ECTI)的基底上皮中显现,该界面将基底上皮与下方的固有层分隔开来。由于局灶性上皮扩张和固有层的蛋白水解重塑,ECTI在早期肿瘤形成过程中会发生显著变形,但很少有研究探讨这些变化。在本研究中,我们使用体内体积多光子自发荧光显微镜和二次谐波产生显微镜对发育异常中ECTI的地形变化进行了定量分析。这种无标记方法能够在不干扰上皮的情况下直接对ECTI表面进行非侵入性可视化。我们描述了一个基于图像的参数“ECTI轮廓”,它可指示ECTI表面的变形情况。发育异常标本中的ECTI轮廓高于对照或炎症标本,表明其表面从平坦转变为变形。我们还测量了基底上皮细胞核面积、核密度、核面积变异系数以及ECTI相邻区域的胶原密度等细胞参数。ECTI轮廓区分发育异常与对照/良性黏膜的敏感性和特异性高于基底核密度或基底核面积,与核面积变异系数和胶原密度相当。所提出的方法为在完整黏膜中研究ECTI提供了独特机会,可同时评估细胞和细胞外基质特征,拓展了对这一关键界面附近早期肿瘤事件的研究机会,并有可能推动体内肿瘤检测新方法的开发。《癌症研究》;76(16);4637 - 47。©2016美国癌症研究协会。