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A non-invasive approach for monitoring breast tumor cells during therapeutic intervention.

机译:一种在治疗干预期间监测乳腺肿瘤细胞的非侵入性方法。

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OBJECTIVE: This study was performed to develop a non-invasive imaging method to evaluate non-palpable tumors in a breast xenograft model undergoing therapy. METHODS: Human breast cancer cells were infected with an adenoviral (Ad) vector encoding enhanced Green Fluorescent Protein (GFP). GFP-positive breast cancer cells were treated with doxorubicin 12 h after plating cells and sequentially imaged. Nude mice were implanted with GFP-positive tumor cells, treated with doxorubicin 24 h after implantation, and imaged at 1, 3, and 5 days after treatment. In vitro and in vivo images of the GFP-positive cells were collected using an inverted microscope and a fluorescent stereomicroscope, respectively. The fluorescence of GFP and of doxorubicin was simultaneously detected using two different GFP filters. RESULTS: Over 99% of tumor cells were GFP-positive following Ad-GFP infection. Doxorubicin therapy killed GFP-positive cancer cells and gradually eliminated GFP fluorescence in vitro and in vivo. Loss of GFP fluorescence was verified as cell death. Incorporation of doxorubicin into tumor cells and detection of single GFP-positive cells was observed in vivo through light-based imaging. CONCLUSION: The response of GFP-positive breast tumor cells to doxorubicin treatment was non-invasively imaged using light-based microscopy. This approach provides many useful applications for the evaluation of new anti-tumor drugs.
机译:目的:本研究旨在开发一种非侵入性成像方法,以评估正在接受治疗的乳腺癌异种移植模型中不可触及的肿瘤。方法:用编码增强型绿色荧光蛋白(GFP)的腺病毒(Ad)载体感染人乳腺癌细胞。铺板细胞后12小时,用阿霉素处理GFP阳性乳腺癌细胞,并进行顺序成像。裸鼠植入GFP阳性肿瘤细胞,植入后24小时用阿霉素处理,并在处理后的1、3和5天成像。分别使用倒置显微镜和荧光立体显微镜收集GFP阳性细胞的体外和体内图像。使用两种不同的GFP滤光片同时检测GFP和阿霉素的荧光。结果:Ad-GFP感染后超过99%的肿瘤细胞为GFP阳性。阿霉素治疗可杀死GFP阳性癌细胞,并在体内和体外逐渐消除GFP荧光。证实GFP荧光的丧失是细胞死亡。通过光成像在体内观察到将阿霉素掺入肿瘤细胞并检测到单个GFP阳性细胞。结论:利用光镜观察了GFP阳性乳腺肿瘤细胞对阿霉素治疗的反应。这种方法为评估新的抗肿瘤药物提供了许多有用的应用。

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