Becker Lucas, Janssen Nicole, Layland Shannon L, Mürdter Thomas E, Nies Anne T, Schenke-Layland Katja, Marzi Julia
Department for Medical Technologies and Regenerative Medicine, Institute of Biomedical Engineering, University of Tübingen, 72076 Tübingen, Germany.
Cluster of Excellence iFIT (EXC 2180) "Image-Guided and Functionally Instructed Tumor Therapies", University of Tübingen, 72076 Tübingen, Germany.
Cancers (Basel). 2021 Nov 13;13(22):5682. doi: 10.3390/cancers13225682.
Hurdles for effective tumor therapy are delayed detection and limited effectiveness of systemic drug therapies by patient-specific multidrug resistance. Non-invasive bioimaging tools such as fluorescence lifetime imaging microscopy (FLIM) and Raman-microspectroscopy have evolved over the last decade, providing the potential to be translated into clinics for early-stage disease detection, in vitro drug screening, and drug efficacy studies in personalized medicine. Accessing tissue- and cell-specific spectral signatures, Raman microspectroscopy has emerged as a diagnostic tool to identify precancerous lesions, cancer stages, or cell malignancy. In vivo Raman measurements have been enabled by recent technological advances in Raman endoscopy and signal-enhancing setups such as coherent anti-stokes Raman spectroscopy or surface-enhanced Raman spectroscopy. FLIM enables in situ investigations of metabolic processes such as glycolysis, oxidative stress, or mitochondrial activity by using the autofluorescence of co-enzymes NADH and FAD, which are associated with intrinsic proteins as a direct measure of tumor metabolism, cell death stages and drug efficacy. The combination of non-invasive and molecular-sensitive in situ techniques and advanced 3D tumor models such as patient-derived organoids or microtumors allows the recapitulation of tumor physiology and metabolism in vitro and facilitates the screening for patient-individualized drug treatment options.
有效的肿瘤治疗面临诸多障碍,包括检测延迟以及患者特异性多药耐药导致的全身药物治疗效果有限。在过去十年中,诸如荧光寿命成像显微镜(FLIM)和拉曼显微光谱等非侵入性生物成像工具不断发展,具备了转化应用于临床以进行早期疾病检测、体外药物筛选以及个性化医学中的药物疗效研究的潜力。拉曼显微光谱能够获取组织和细胞特异性光谱特征,已成为一种用于识别癌前病变、癌症分期或细胞恶性程度的诊断工具。近期拉曼内窥镜技术以及诸如相干反斯托克斯拉曼光谱或表面增强拉曼光谱等信号增强装置的技术进步,使得体内拉曼测量得以实现。FLIM通过利用辅酶NADH和FAD的自发荧光,能够对糖酵解、氧化应激或线粒体活性等代谢过程进行原位研究,这些辅酶与内在蛋白质相关联,可直接作为肿瘤代谢、细胞死亡阶段和药物疗效的度量指标。非侵入性和分子敏感的原位技术与先进的3D肿瘤模型(如患者来源的类器官或微肿瘤)相结合,能够在体外重现肿瘤生理和代谢情况,并有助于筛选患者个体化的药物治疗方案。