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对体外X射线诱导转化不同阶段分离出的DNA进行分子分析。

Molecular analysis of DNA isolated from the different stages of x-ray-induced transformation in vitro.

作者信息

Krolewski B, Little J B

机构信息

Laboratory of Radiobiology, Harvard School of Public Health, Boston, Massachusetts 02115.

出版信息

Mol Carcinog. 1989;2(1):27-33. doi: 10.1002/mc.2940020105.

DOI:10.1002/mc.2940020105
PMID:2730762
Abstract

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.

摘要

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。

相似文献

1
Molecular analysis of DNA isolated from the different stages of x-ray-induced transformation in vitro.对体外X射线诱导转化不同阶段分离出的DNA进行分子分析。
Mol Carcinog. 1989;2(1):27-33. doi: 10.1002/mc.2940020105.
2
Distinctive transforming genes in x-ray-transformed mammalian cells.X射线转化的哺乳动物细胞中的独特转化基因。
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Hamster cell line suitable for transfection assay of transforming genes.适用于转化基因转染分析的仓鼠细胞系。
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引用本文的文献

1
Osteosarcomagenic doses of radium (224Ra) and infectious endogenous retroviruses enhance proliferation and osteogenic differentiation of skeletal tissue differentiating in vitro.致癌剂量的镭(224Ra)和传染性内源性逆转录病毒可增强体外分化的骨骼组织的增殖和成骨分化。
Radiat Environ Biophys. 1994;33(1):69-79. doi: 10.1007/BF01255275.
2
Inducible cellular responses to ultraviolet light irradiation and other mediators of DNA damage in mammalian cells.哺乳动物细胞对紫外线照射及其他DNA损伤介质的诱导性细胞反应。
Cell Biol Toxicol. 1990 Jan;6(1):105-26. doi: 10.1007/BF00135030.
3
Differential gene expression during multistage carcinogenesis.
多阶段致癌过程中的差异基因表达。
Environ Health Perspect. 1991 Jun;93:51-6. doi: 10.1289/ehp.919351.
4
Oncogenes and radiation carcinogenesis.癌基因与辐射致癌作用
Environ Health Perspect. 1991 Jun;93:45-9. doi: 10.1289/ehp.919345.