Krolewski B, Little J B
Laboratory of Radiobiology, Harvard School of Public Health, Boston, Massachusetts 02115.
Mol Carcinog. 1989;2(1):27-33. doi: 10.1002/mc.2940020105.
A major challenge in radiation carcinogenesis is to identify the cellular gene or genes involved in initiating the process. We examined the transforming activities of DNAs obtained from C3H10T1/2 cells during x-ray-induced morphological transformation. DNAs extracted from mass cultures of 10T1/2 cells at different times after irradiation with 600 rad and from type III-transformed foci were transfected into NIH 3T3 cells. The results indicate that certain oncogenes are activated beginning 3 wk after irradiation, well before the appearance of macroscopically visible transformed foci. For DNA isolated from x-ray-transformed 10T1/2 cells (type III foci), the frequencies of transfection were 0.003-0.11 foci/microgram of genomic DNA with NIH 3T3 cells and 0.004-0.04 foci/microgram genomic DNA using 10T1/2 cells as recipients. Southern blot analysis of DNAs obtained from 23 primary transfectants and from 23 x-ray-transformed cell lines indicated no gross rearrangements or amplification of any of the 14 oncogenes screened (v-Ha-ras, v-Ki-ras, N-ras, v-myc, v-raf, v-src, v-fes, v-abl, v-mos, v-erbA, v-erbB, v-myb, v-fos, v-sis). This suggests that x-irradiation may activate as yet unidentified oncogenes. The occurrence of positive transfection 3 wk after irradiation is discussed in terms of the hypothesis that transformation may not occur as a direct consequence of the exposure to x-rays but develops as a rare event in the progeny of the irradiated cells at some later time, as a consequence of the delayed activation of certain genes.
辐射致癌作用中的一个主要挑战是确定启动该过程所涉及的一个或多个细胞基因。我们检测了在X射线诱导的形态转化过程中从C3H10T1/2细胞获得的DNA的转化活性。从600拉德照射后不同时间的10T1/2细胞大量培养物以及III型转化灶中提取的DNA被转染到NIH 3T3细胞中。结果表明,某些癌基因在照射后3周开始被激活,远在宏观可见的转化灶出现之前。对于从X射线转化的10T1/2细胞(III型灶)分离的DNA,以NIH 3T3细胞作为受体时,转染频率为0.003 - 0.11个灶/微克基因组DNA,以10T1/2细胞作为受体时为0.004 - 0.04个灶/微克基因组DNA。对从23个原代转染子和23个X射线转化细胞系获得的DNA进行的Southern印迹分析表明,所筛选的14个癌基因(v-Ha-ras、v-Ki-ras、N-ras、v-myc、v-raf、v-src、v-fes、v-abl、v-mos、v-erbA、v-erbB、v-myb、v-fos、v-sis)均未发生明显重排或扩增。这表明X射线照射可能激活了尚未鉴定的癌基因。根据以下假设讨论了照射后3周出现阳性转染的情况:转化可能不是暴露于X射线的直接后果,而是在照射细胞的后代中在稍后某个时间作为罕见事件发生,这是某些基因延迟激活的结果。