Teicher Beverly A
Genzyme Corporation, 1 Mountain Road, Framingham, MA 01701, USA.
Mol Cancer Ther. 2006 Oct;5(10):2435-43. doi: 10.1158/1535-7163.MCT-06-0391.
The first in vivo tumor models were developed in the mid-1960s. These models were mouse leukemia models grown as ascites. The growth pattern was like that of bacteria in vivo and therefore it was possible to apply similar mathematics of growth and response to these tumors as had been worked out for bacteria. Since the development of the murine leukemia models, investigators have devoted a large effort to modeling solid tumors in mice. There are now a variety of models including syngeneic mouse tumors and human tumor xenografts grown as s.c. nodules, syngeneic mouse tumors and human tumor xenografts grown in orthotopic sites, models of disseminated disease, "labeled" tumor models that can be visualized using varied technologies, and transgenic tumor models. Each of these types of models has advantages and disadvantages to the "drug hunter" searching for improved treatments.
首个体内肿瘤模型于20世纪60年代中期建立。这些模型是作为腹水生长的小鼠白血病模型。其生长模式与体内细菌的生长模式相似,因此有可能将已应用于细菌的类似生长和反应数学方法应用于这些肿瘤。自小鼠白血病模型建立以来,研究人员在小鼠实体瘤建模方面投入了大量精力。现在有多种模型,包括作为皮下结节生长的同基因小鼠肿瘤和人肿瘤异种移植模型、在原位生长的同基因小鼠肿瘤和人肿瘤异种移植模型、播散性疾病模型、可使用各种技术可视化的“标记”肿瘤模型以及转基因肿瘤模型。对于寻求改进治疗方法的“药物研发人员”而言,每种类型的模型都有其优缺点。