...
首页> 外文期刊>Tumour biology : >A superficial colon tumor model involving subcutaneous colon translocation and orthotopic transplantation of green fluorescent protein-expressing human colon tumor.
【24h】

A superficial colon tumor model involving subcutaneous colon translocation and orthotopic transplantation of green fluorescent protein-expressing human colon tumor.

机译:一种浅表结肠肿瘤模型,涉及皮下结肠移位和表达绿色荧光蛋白的人结肠肿瘤的原位移植。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The orthotopic transplantation model of human tumor has been demonstrated to be more patient-like animal tumor model. However, observations of tumor progression and metastasis are limited by the deep location of the colon or limited deep penetration ability of fluorescence through tissue. The purpose of this study is to establish a superficial orthotopic model to allow easier real-time visualization and more sensitive monitoring of fluorescent orthotopic colon tumor. Human colon cancer HT-29 cells were transduced with a pLPCX expression retroviral vector containing green fluorescent protein and neomycin resistance genes. For superficial orthotopic transplantation model, the cecum was identified and pulled out of the peritoneal cavity, the space between the cecum and peritoneum was sutured, the cecum was pulled to subcutaneous tissue, and incision was made on the cecal serosa followed by the implantation of a 1-mm tumor tissue to the cecum. For comparison, a conventional orthotopic transplantation model was established in a separate group of mice simultaneously. When tumor sizes reached 5 mm in diameter, half the mice in each model received 5-FU treatment. Primary tumor and metastases were monitored by fluorescent imaging or caliber measurement. Tumor fluorescence was observed as early as 3 days (median time of 4.7 +/- 1.3 days) post-transplantation in the superficial orthotopic transplantation model, which was much earlier than 21 days (median time of 26.2 +/- 9.9 days) in conventional orthotopic transplantation model. Although tumor growth of 5-FU-treated mice in conventional orthotopic model was lower than those of the untreated mice, the difference was not significant. However, in superficial orthotopic model, tumor growth was significantly inhibited in 5-FU-treated mice relative to the untreated mice. Fluorescence imaging showed similar metastasis incidence between the superficial and conventional orthotopic transplantation models. The fluorescent superficial orthotopic transplantation colon model allows easier real-time visualization and more sensitive monitoring of tumor growth as well as convenient repeated sampling. It is a valuable orthotopic implantation model for study of colon cancer and evaluation of new anti-cancer therapy.
机译:人类肿瘤的原位移植模型已被证明是更像患者的动物肿瘤模型。然而,对肿瘤进展和转移的观察受到结肠深处位置或荧光通过组织的深层穿透能力的限制。这项研究的目的是建立一个浅表的原位模型,以使荧光原位结肠癌的实时可视化和敏感监测更加容易。用含有绿色荧光蛋白和新霉素抗性基因的pLPCX表达逆转录病毒载体转导人结肠癌HT-29细胞。对于浅表原位移植模型,确定盲肠并从腹膜腔中拉出,缝合盲肠和腹膜之间的空间,将盲肠拉到皮下组织,在盲肠浆膜上切开切口,然后植入盲肠1mm肿瘤组织。为了进行比较,同时在单独的一组小鼠中建立了常规的原位移植模型。当肿瘤直径达到5毫米时,每种模型中的一半小鼠接受5-FU治疗。通过荧光成像或口径测量监测原发性肿瘤和转移。在浅表原位移植模型中,最早在移植后3天(中间时间为4.7 +/- 1.3天)就观察到了肿瘤荧光,这比常规的21天(中间时间为26.2 +/- 9.9天)要早得多。原位移植模型。尽管在常规原位模型中用5-FU处理的小鼠的肿瘤生长低于未处理小鼠的肿瘤生长,但差异并不显着。但是,在浅表原位模型中,相对于未治疗的小鼠,经5-FU治疗的小鼠的肿瘤生长受到明显抑制。荧光成像显示浅表和常规原位移植模型之间的转移发生率相似。荧光浅表原位移植结肠模型可以更轻松地进行实时可视化,对肿瘤生长进行更灵敏的监测,并方便重复采样。这是用于结肠癌研究和评估新抗癌治疗的有价值的原位植入模型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号