Warenius H M, Bleehen N M
Br J Cancer. 1982 Jul;46(1):45-50. doi: 10.1038/bjc.1982.163.
The HT29R human colonic adenocarcinoma cell line grows as locally invasive, mucin-secreting tumours in immunosuppressed mice with a doubling time of 6 days. These tumours may be disaggregated to give single-cell suspensions with plating efficiencies of 25-45% in technically simple in vivo-in vitro cell-survival assays. The effect of maximum tolerated doses of 5-fluorouracil, melphalan and cyclo-phosphamide on in situ growth is only slight. In vivo-in vitro cell-survival assays phosphamide on in situ growth is only slight. In vivo-in vitro cell-survival assays are consistent with these in situ results. The relative ease of experimental manipulation and the high clonogenic efficiency of this tumour make it a useful addition to human tumour xenograft models.
HT29R人结肠腺癌细胞系在免疫抑制小鼠体内生长为局部浸润性、分泌粘蛋白的肿瘤,倍增时间为6天。在技术简单的体内-体外细胞存活试验中,这些肿瘤可以被解离成单细胞悬液,接种效率为25%-45%。5-氟尿嘧啶、美法仑和环磷酰胺的最大耐受剂量对原位生长的影响很小。体内-体外细胞存活试验与这些原位结果一致。这种肿瘤实验操作相对简便且克隆形成效率高,使其成为人类肿瘤异种移植模型中的有用补充。