Stein U, Walther W, Wunderlich V
Laboratory of Drug Discovery Research and Development, National Cancer Institute, Frederick Cancer Research and Development Center, MD 21702-1201.
Eur J Cancer. 1994;30A(10):1541-5. doi: 10.1016/0959-8049(94)00287-f.
Among human sarcomas, osteosarcomas usually display high intrinsic mdr1 expression while malignant fibrous histiocytomas (MFH) do not. A comparative polymerase chain reaction (PCR)-based sequence analysis of the mdr1 promoter revealed point mutations in seven out of nine osteosarcomas at nucleotides +103 (2 cases T-->C) and +137 (5 cases G-->T). No changes were seen in eight MFHs. When COS cells transfected with CAT constructs containing the T-->C chloramphenicol acetyltransferase mutant mdr1 promoters were treated with vincristine or doxorubicin, expression of the CAT gene was enhanced to a higher extent than with constructs containing wild-type or G-->T-mutant mdr1 promoters. We suggest that there is a correlation between the type of mdr1 promoter mutation and responsiveness to MDR relevant drugs.
在人类肉瘤中,骨肉瘤通常显示出较高的内在mdr1表达,而恶性纤维组织细胞瘤(MFH)则不然。基于聚合酶链反应(PCR)的mdr1启动子序列比较分析显示,9例骨肉瘤中有7例在核苷酸+103(2例T→C)和+137(5例G→T)处发生点突变。8例MFH中未见变化。当用长春新碱或阿霉素处理转染了含有T→C氯霉素乙酰转移酶突变型mdr1启动子的CAT构建体的COS细胞时,CAT基因的表达比含有野生型或G→T突变型mdr1启动子的构建体增强的程度更高。我们认为mdr1启动子突变类型与对多药耐药相关药物的反应性之间存在相关性。