分类
+ 血管生成
+ 癌症生物化学
+ 癌症干细胞
+ 细胞周期检查点(checkpoint)
+ 细胞死亡
+ 细胞能量学
+ 通用技术
+ 基因组不稳定性及突变
+ 炎症
+ 侵袭和转移
+ 微环境
+ 瘤形成
+ 增殖信号转导
+ 无限复制
- 肿瘤免疫学
+ 动物模型
+ 生物化学试验
+ 癌症治疗
+ 细胞生物学试验
药物发现和分析
+ 免疫学试验
- 肿瘤形成
细胞分离和检测
+ 肿瘤微环境
往期刊物

In vivo Efficacy Studies in Cell Line and Patient-derived Xenograft Mouse Models

在细胞系和患者源性异种移植瘤小鼠模型中进行的体内疗效研究

ET Elizabeth A. Tovar
CE Curt J. Essenburg
CG Carrie Graveel
17231 Views
Jan 5, 2017
In vivo xenograft models derived from human cancer cells have been a gold standard for evaluating the genetic drivers of cancer and are valuable preclinical models for evaluating the efficacy of cancer therapeutics. Recently, patient-derived tumorgrafts from multiple tumor types have been developed and shown to more accurately recapitulate the molecular and histological heterogeneity of cancer. Here we detail the procedures for developing patient-derived xenograft models from breast cancer tissue, cell-based xenograft models, serial tumor transplantation, tumor measurement, and drug treatment.

In vivo Bioluminescence Imaging of Luciferase-labeled Cancer Cells

荧光素酶标记癌细胞的体内生物发光成像

Marc Carceles-Cordon Marc Carceles-Cordon
Irene Rodriguez-Fernandez Irene Rodriguez-Fernandez
Veronica Rodriguez-Bravo Veronica Rodriguez-Bravo
CC Carlos Cordon-Cardo
Josep Domingo-Domenech Josep Domingo-Domenech
37652 Views
Mar 20, 2016
Over the past decade, in vivo bioluminescent imaging has emerged as a non-invasive and sensitive tool for studying ongoing biological processes within living organisms (Contag et al., 1997; Contag et al., 1998). Based on the detection and quantitation of the photons produced by the oxidation of luciferin by luciferase enzymes (Harvey, 1927), this technique has proved to be particularly useful in analyzing cancerous cells and monitoring tumor growth (Edinger et al., 1999; Sweeney et al., 1999; Vidal et al., 2015), providing a cost-effective insight into how the disease progresses in vivo, without the need of serial sacrifice of animals. This protocol describes in detail the procedure of obtaining luciferase-tagged tumors in immunocompromised mice that can be studied by bioluminescent imaging through the use of an IVIS Spectrum imager.