TY - JOUR
T1 - Remodeling of the epithelial-connective tissue interface in oral epithelial dysplasia as visualized by noninvasive 3D imaging
AU - Pal, Rahul
AU - Shilagard, Tuya
AU - Yang, Jinping
AU - Villarreal, Paula
AU - Brown, Tyra
AU - Qiu, Suimin
AU - McCammon, Susan
AU - Resto, Vicente
AU - Vargas, Gracie
N1 - Publisher Copyright:
© 2016 American Association for Cancer Research.
PY - 2016/8/15
Y1 - 2016/8/15
N2 - 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.
AB - 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.
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U2 - 10.1158/0008-5472.CAN-16-0252
DO - 10.1158/0008-5472.CAN-16-0252
M3 - Article
C2 - 27302162
AN - SCOPUS:84982130992
SN - 0008-5472
VL - 76
SP - 4637
EP - 4647
JO - Cancer Research
JF - Cancer Research
IS - 16
ER -