Hanania N, Boyano M D, Mangin C, Poupon M F
Biologie des Métastases, IRSC-CNRS, Villejuif, France.
Anticancer Res. 1991 Jan-Feb;11(1):473-80.
The expression of various protooncogenes (myc, Ki-ras, Ha-ras, erbB, fms, sis, jun and fos) and a gene implicated in multidrug resistance (mdr1) was investigated in cell sublines, isolated from a rat rhabdomyosarcoma cell line, and in the corresponding tumors induced by injection of these cells into syngeneic rats. These cell lines and tumors, selected or not by treatment with chlorozotocin (Czt) or adriamycin (Adr), differed in their tumorigenicities and metastatic potentials. Our results showed that 1) an increased expression of some protooncogenes could be correlated with the metastatic potential of tumors; 2) such a correlation was not observed in the cultured cells from which these tumors were derived; 3) mdr1 expression, similarly to that of protooncogenes, was correlated with metastatic potential in all tumors except the Adr-selected tumors.
在从大鼠横纹肌肉瘤细胞系分离得到的细胞亚系以及将这些细胞注射到同基因大鼠体内诱导产生的相应肿瘤中,研究了各种原癌基因(myc、Ki-ras、Ha-ras、erbB、fms、sis、jun和fos)以及一个与多药耐药相关的基因(mdr1)的表达情况。这些细胞系和肿瘤,无论是否经氯脲菌素(Czt)或阿霉素(Adr)处理筛选,其致瘤性和转移潜能均有所不同。我们的结果表明:1)某些原癌基因表达的增加可能与肿瘤的转移潜能相关;2)在这些肿瘤所源自的培养细胞中未观察到这种相关性;3)mdr1的表达与原癌基因类似,在除阿霉素筛选的肿瘤外的所有肿瘤中均与转移潜能相关。