首页> 外文会议>Optical Biopsy VI; Progress in Biomedical Optics and Imaging; vol.7 no.14 >In vivo multiphoton and second harmonic generation microscopy of epithelial carcinogenesis
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In vivo multiphoton and second harmonic generation microscopy of epithelial carcinogenesis

机译:上皮癌变的体内多光子和二次谐波产生显微镜

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Multiphoton microscopy and second harmonic generation microscopy were used to image epithelial changes in a hamster model for oral malignant transformation. In vivo imaging was performed to characterize morphometric alterations in normal and precancerous regions. Morphometric measurements such as cell nucleus area and epithelial thicknesses obtained from MPM-SHGM were in excellent agreement with histology obtained after in vivo imaging. MPM-SHGM was highly sensitive to spectroscopic and architectural alterations throughout carcinogenesis, showing statistically significant changes in morphology. MPM revealed hyperkeratosis, nuclear enlargement/crowding in dysplasia, and immune cell infiltration. SHGM revealed alterations in submucosal architecture, with a decrease in SHG density evident during early stages of precancer. By combining MPM with SHGM, the basement membrane could be identified in normal, hyperplasia, and dysplasia samples and in some cases of early invasion. The combined technique of MPM-SHGM has the potential to serve as an adjunct to biopsy for assessing precancerous changes and will be investigated further for that purpose. Additionally, the method can provide spatiotemporal assessment of early neoplastic changes in order to elucidate the stages of transformation in vivo and could be used to assess therapeutic efficacy of agents being tested for the treatment of epithelial precancers/cancer.
机译:使用多光子显微镜和二次谐波显微镜对仓鼠模型中的上皮变化进行成像,以进行口腔恶性转化。进行体内成像以表征正常和癌前区域的形态变化。从MPM-SHGM获得的形态测量值(如细胞核面积和上皮厚度)与体内成像后获得的组织学非常吻合。 MPM-SHGM对整个致癌过程中的光谱和结构变化高度敏感,显示出统计学上显着的形态变化。 MPM显示角化过度,异型增生中的核增大/拥挤以及免疫细胞浸润。 SHGM揭示了粘膜下结构的改变,在癌前期的早期,SHG密度明显降低。通过将MPM与SHGM结合,可以在正常,增生和不典型增生的样本中以及在某些早期侵袭的病例中鉴定出基底膜。 MPM-SHGM的组合技术有可能作为活检的辅助手段,以评估癌前变化,并将对此进行进一步研究。另外,该方法可以提供早期肿瘤变化的时空评估,以便阐明体内转化的阶段,并且可以用于评估被测试用于治疗上皮癌前体/癌症的药剂的治疗功效。

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