Chen H L, Carbone D P
Division of Medical Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
Mol Med Today. 1997 Apr;3(4):160-7. doi: 10.1016/S1357-4310(97)01003-4.
The key to specific and non-toxic cancer therapy is likely to be identification and targeting of processes that are absolutely unique to the tumor. One such approach is to target cells expressing mutations in the oncoproteins that led to the development of the cancer, such as p53. In animal model systems, highly mutant p53-specific cytotoxic T cells can be induced, but it remains to be seen whether this can be translated into clinical practice, and what proportion of tumors will respond. In this review, the potential and problems of immunological targeting of mutant p53 in solid tumors are discussed.
特异性且无毒的癌症治疗的关键可能在于识别并靶向肿瘤特有的过程。一种这样的方法是靶向表达导致癌症发生的癌蛋白(如p53)突变的细胞。在动物模型系统中,可以诱导出高度针对突变型p53的细胞毒性T细胞,但这能否转化为临床实践以及有多大比例的肿瘤会产生反应仍有待观察。在这篇综述中,将讨论实体瘤中突变型p53免疫靶向治疗的潜力和问题。