Xu Xiaoyun, Cheng Jie, Thrall Michael J, Liu Zhengfan, Wang Xi, Wong Stephen T C
Systems Medicine and Bioengineering Department, Houston Methodist Research Institute, Weill Cornell Medical College, Houston, Texas 77030 USA ; Authors contributed equally to this work.
Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Weill Cornell Medical College, Houston, Texas 77030 USA.
Biomed Opt Express. 2013 Nov 15;4(12):2855-68. doi: 10.1364/BOE.4.002855. eCollection 2013.
Lung carcinoma is the leading cause of cancer-related death in the United States, and non-small cell carcinoma accounts for 85% of all lung cancer cases. One major characteristic of non-small cell carcinoma is the appearance of desmoplasia and deposition of dense extracellular collagen around the tumor. The desmoplastic response provides a radiologic target but may impair sampling during traditional image-guided needle biopsy and is difficult to differentiate from normal tissues using single label free imaging modality; for translational purposes, label-free techniques provide a more promising route to clinics. We thus investigated the potential of using multimodal, label free optical microscopy that incorporates Coherent Anti-Stokes Raman Scattering (CARS), Two-Photon Excited AutoFluorescence (TPEAF), and Second Harmonic Generation (SHG) techniques for differentiating lung cancer from normal and desmoplastic tissues. Lung tissue samples from patients were imaged using CARS, TPEAF, and SHG for comparison and showed that the combination of the three non-linear optics techniques is essential for attaining reliable differentiation. These images also illustrated good pathological correlation with hematoxylin and eosin (H&E) stained sections from the same tissue samples. Automated image analysis algorithms were developed for quantitative segmentation and feature extraction to enable lung tissue differentiation. Our results indicate that coupled with automated morphology analysis, the proposed tri-modal nonlinear optical imaging technique potentially offers a powerful translational strategy to differentiate cancer lesions reliably from surrounding non-tumor and desmoplastic tissues.
肺癌是美国癌症相关死亡的主要原因,非小细胞癌占所有肺癌病例的85%。非小细胞癌的一个主要特征是肿瘤周围出现促结缔组织增生和致密细胞外胶原蛋白沉积。促结缔组织增生反应提供了一个放射学靶点,但可能会影响传统图像引导下针吸活检的取样,并且使用单一的无标记成像模式很难与正常组织区分开来;为了实现转化应用,无标记技术为临床应用提供了更有前景的途径。因此,我们研究了使用结合了相干反斯托克斯拉曼散射(CARS)、双光子激发自发荧光(TPEAF)和二次谐波产生(SHG)技术的多模态无标记光学显微镜来区分肺癌与正常组织和促结缔组织增生组织的潜力。对患者的肺组织样本进行了CARS、TPEAF和SHG成像以作比较,结果表明这三种非线性光学技术的结合对于实现可靠的区分至关重要。这些图像还显示出与来自相同组织样本的苏木精和伊红(H&E)染色切片具有良好的病理相关性。开发了自动图像分析算法用于定量分割和特征提取,以实现肺组织的区分。我们的结果表明,结合自动形态分析,所提出的三模态非线性光学成像技术有可能提供一种强大的转化策略,以可靠地将癌性病变与周围的非肿瘤组织和促结缔组织增生组织区分开来。