Department of Biomedical Engineering, Texas A&M University, College Station, TX 77840, USA.
IEEE Trans Biomed Eng. 2010 Oct;57(10):2596-9. doi: 10.1109/TBME.2010.2060485. Epub 2010 Jul 23.
Early detection of cancer is key to reducing morbidity and mortality. Morphological and chemical biomarkers presage the transition from normal to cancerous tissue. We have developed a noninvasive imaging system incorporating optical coherence tomography (OCT) and fluorescence lifetime imaging microscopy (FLIM) into a single optical system for the first time, in order to acquire both sets of biomarkers. OCT can provide morphological images of tissue with high resolution, while FLIM can provide biochemical tissue maps. Coregistered OCT volumes and FLIM images have been acquired simultaneously in an in vivo hamster cheek pouch model of oral cancer. The OCT images indicate morphological biomarkers for cancer including thickening of the epithelial layer and loss of the layered structure. The FLIM images indicate chemical biomarkers including increased nicotinamide adenine dinucleotide and reduced collagen emission. While both sets of biomarkers can differentiate normal and cancerous tissue, we believe their combination will enable the discrimination of benign lesions possessing some of the indicated biomarkers, e.g., scarring or inflammation.
癌症的早期检测是降低发病率和死亡率的关键。形态和化学生物标志物预示着正常组织向癌变组织的转变。我们首次开发了一种将光学相干断层扫描(OCT)和荧光寿命成像显微镜(FLIM)集成到单个光学系统中的非侵入性成像系统,以便同时获取这两种生物标志物。OCT 可以提供具有高分辨率的组织形态图像,而 FLIM 可以提供生化组织图谱。我们在体内仓鼠颊囊口腔癌模型中同时获取 OCT 体积和 FLIM 图像。OCT 图像显示了癌症的形态学生物标志物,包括上皮层增厚和分层结构的丧失。FLIM 图像显示了包括烟酰胺腺嘌呤二核苷酸增加和胶原蛋白发射减少在内的化学生物标志物。虽然这两种生物标志物都可以区分正常组织和癌变组织,但我们相信它们的组合将能够区分具有某些指示生物标志物的良性病变,例如疤痕或炎症。