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首页> 外文期刊>Oncology letters >Intravital imaging of the effects of 5-fluorouracil on the murine liver microenvironment using 2-photon laser scanning microscopy
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Intravital imaging of the effects of 5-fluorouracil on the murine liver microenvironment using 2-photon laser scanning microscopy

机译:使用2-光子激光扫描显微镜对5-氟尿嘧啶对小鼠肝脏微环境的影响进行体内成像

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摘要

5-fluorouracil (5FU) is often used in the treatment of colorectal cancer. 5FU improves the median overall and disease-free survival rates and reduces recurrence rates in patients who have undergone curative surgical resection. However, in the adjuvant setting, whether 5FU eradicates clinically undetectable micrometastases in target organs such as the liver, or whether 5-FU inhibits the adhesion of circulating tumor cells has not yet been established. In the present study, 5FU was administered following the inoculation of red fluorescent protein-expressing HT29 cells into green fluorescent protein (GFP)-transgenic nude mice to examine its inhibitory effect. 2-photon laser scanning microscopy was performed at selected time points for time-series imaging of liver metastasis of GFP-transgenic mice. The cell number in vessels was quantified to evaluate the response of the tumor microenvironment to chemotherapy. HT29 cells were visualized in hepatic sinusoids at the single-cell level. A total of 2 hours after the injection (early stage), time-series imaging revealed that the number of caught tumor cells gradually reduced over time. In the 5FU treatment group, no significant difference was observed in the cell number in the early stage. One week after the injection (late stage), a difference in morphology was observed. The results of the present study indicated that 5FU eradicated clinically undetectable micrometastases in liver tissues by acting as a cytotoxic agent opposed to preventing adhesion. The present study indicated that time-series intravital 2-photon laser scanning microscopic imaging of metastatic tumor xenografts may facilitate the screening and evaluation of novel chemotherapeutic agents with less interindividual variability.
机译:5-氟尿嘧啶(5FU)通常用于治疗大肠癌。 5FU可提高接受根治性手术切除的患者的总体中位和无病生存率,并降低复发率。然而,在佐剂中,尚未确定5FU是否根除目标器官(如肝脏)中临床上无法检测到的微转移,或5-FU是否抑制循环肿瘤细胞的粘附。在本研究中,将表达红色荧光蛋白的HT29细胞接种到绿色荧光蛋白(GFP)转基因裸鼠中后,给予5FU,以检查其抑制作用。在选定的时间点进行2光子激光扫描显微镜检查,以便对GFP转基因小鼠的肝转移进行时序成像。量化血管中的细胞数以评估肿瘤微环境对化学疗法的反应。 HT29细胞在肝窦中以单细胞水平可见。注射后(早期)总共2个小时,时间序列成像显示捕获的肿瘤细胞数量随时间逐渐减少。在5FU治疗组中,早期的细胞数没有显着差异。注射后一周(晚期),观察到形态学差异。本研究的结果表明,5FU通过充当细胞毒剂而不是防止粘连,从而消除了肝组织中临床上无法检测到的微转移。本研究表明,转移性肿瘤异种移植物的时间序列活体2光子激光扫描显微成像可能有助于筛选和评估个体差异较小的新型化疗药物。

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