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5-氟尿嘧啶、伊立替康和/或肿瘤坏死因子相关凋亡诱导配体处理的新鲜人结肠上皮细胞死亡的无创荧光成像

Non-invasive fluorescence imaging of cell death in fresh human colon epithelia treated with 5-Fluorouracil, CPT-11 and/or TRAIL.

作者信息

Finnberg Niklas, Kim Seok-Hyun, Furth Emma E, Liu Jue Judy, Russo Pierre, Piccoli David A, Grimberg Adda, El-Deiry Wafik S

机构信息

Abramson Comprehensive Cancer Center, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

出版信息

Cancer Biol Ther. 2005 Sep;4(9):937-42. doi: 10.4161/cbt.4.9.2182. Epub 2005 Sep 18.

Abstract

Apoptosis is instrumental in several physiological/pathophysiological processes and is a frequently used end-point in the development of anti-neoplastic compounds. Despite ample data on several colon cancer cell lines, little is known about the susceptibility of human colon to apoptosis following treatment with established chemotherapeutics. By treating fresh human colonic explants with 5-Fluorouracil (200 microg/ml), CPT-11 (100 microg/ml) and/or TRAIL (100 ng/ml) we readily detected a signal in situ using FITC-VAD-FMK at different time points, whereas labeling of colonic explants with EGFP-conjugated Annexin V proved less specific. Although TRAIL treatment alone appeared to cause little apoptosis in human colonic epithelia versus the control, we observed a greater number of cells undergoing apoptosis when a combination of CPT-11 and TRAIL was used as compared to either agent alone. This is the initial demonstration of TRAIL-induced apoptosis with or without a chemotherapeutic agent in fresh primary human colon epithelia explants. Thus, human colonic explants may provide a valuable reference point when candidate therapeutic compounds triggering apoptosis in colon cancer cell lines, xenografts or mouse models are developed. The results support the feasibility of developing non-invasive optical imaging strategies to detect apoptosis through direct visualization of injury to human colonic epithelia in vivo.

摘要

细胞凋亡在多个生理/病理生理过程中发挥作用,并且是抗肿瘤化合物研发中常用的终点指标。尽管已有关于多种结肠癌细胞系的大量数据,但对于用既定化疗药物处理后人类结肠对细胞凋亡的易感性却知之甚少。通过用5-氟尿嘧啶(200微克/毫升)、伊立替康(100微克/毫升)和/或肿瘤坏死因子相关凋亡诱导配体(TRAIL,100纳克/毫升)处理新鲜的人类结肠外植体,我们在不同时间点使用异硫氰酸荧光素-缬氨酸-天冬氨酸-氟甲基酮(FITC-VAD-FMK)很容易地原位检测到了信号,而用绿色荧光蛋白(EGFP)偶联的膜联蛋白V标记结肠外植体的特异性较差。尽管单独使用TRAIL处理与对照组相比似乎在人类结肠上皮中几乎不引起细胞凋亡,但我们观察到,与单独使用任何一种药物相比,当联合使用伊立替康和TRAIL时,发生凋亡的细胞数量更多。这是在新鲜的原发性人类结肠上皮外植体中首次证明TRAIL诱导的细胞凋亡,无论有无化疗药物。因此,在开发能在结肠癌细胞系、异种移植模型或小鼠模型中触发细胞凋亡的候选治疗化合物时,人类结肠外植体可能提供一个有价值的参考点。这些结果支持了开发非侵入性光学成像策略的可行性,该策略可通过直接可视化体内人类结肠上皮损伤来检测细胞凋亡。

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