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体内定量每克隆形成细胞的放射性甲状腺癌发生频率。

Quantifying the frequency of radiogenic thyroid cancer per clonogenic cell in vivo.

作者信息

Domann F E, Freitas M A, Gould M N, Clifton K H

机构信息

Department of Human Oncology, University of Wisconsin Clinical Cancer Center, Madison 53792.

出版信息

Radiat Res. 1994 Mar;137(3):330-7.

PMID:8146276
Abstract

We used quantitative cell transplantation to evaluate the frequencies of the formation of radiogenic thyroid cancer per clonogenic rat thyroid epithelial cell in vivo. Irradiation of thyroid cells with 5 Gy 137Cs gamma rays before transplantation significantly increased the incidence of thyroid carcinoma formation in such grafts compared to similar grafts of unirradiated thyroid cells. We calculated the frequencies of radiogenic cancer by subtracting cancer incidences in unirradiated groups from incidences in irradiated groups and dividing by the number of clonogens grafted. The highest observed frequencies of radiogenic thyroid cancer so calculated were 0.141 and 0.046 cancers per surviving irradiated clonogenic cell. These cancer frequencies occurred in grafts containing averages of three and ten clonogens per site, respectively, and represent one cancer per approximately 7 and approximately 22 irradiated clonogens. We conclude that the highest observed frequencies of radiogenic cancer are likely to be the best estimates of the "real" frequency per irradiated clonogen in that virtually all the methodological sources of inaccuracy tend to decrease the observed frequency compared to the "real" frequency. Radiogenic initiation of cancer is thus a highly common cellular event among surviving irradiated clonogenic thyroid cells. To examine the role of endocrine-mediated tumor promotion on the expression of radiogenic cancer, we attenuated the intensity of thyrotropin (TSH)-mediated tumor promotion in some groups of recipient animals. We found that the incidence rates for radiation-associated cancer were significantly higher in rats with higher serum TSH levels compared to rats with lower TSH levels. We conclude from these data that (1) radiogenic thyroid cancer occurs with a high frequency and (2) chronic TSH stimulation accelerates progression of radiogenic neoplasms to overt carcinomas and promotes development of later-arising carcinomas in grafts of unirradiated thyroid clonogens.

摘要

我们采用定量细胞移植的方法,在体内评估每克隆源性大鼠甲状腺上皮细胞形成放射性甲状腺癌的频率。与未照射甲状腺细胞的类似移植相比,移植前用5 Gy的137Csγ射线照射甲状腺细胞显著增加了此类移植中甲状腺癌形成的发生率。我们通过用照射组的癌症发生率减去未照射组的癌症发生率,再除以移植的克隆原数量来计算放射性癌症的频率。如此计算得出的放射性甲状腺癌的最高观察频率分别为每存活的照射克隆源性细胞0.141例癌症和0.046例癌症。这些癌症频率分别出现在每个位点平均含有3个和10个克隆原的移植中,分别代表每约7个和约22个照射克隆原中有1例癌症。我们得出结论,观察到的放射性癌症的最高频率很可能是每个照射克隆原“真实”频率的最佳估计,因为与“真实”频率相比,几乎所有方法学上的不准确来源都倾向于降低观察到的频率。因此,放射性致癌起始在存活的照射克隆源性甲状腺细胞中是一种非常常见的细胞事件。为了研究内分泌介导的肿瘤促进对放射性癌症表达的作用,我们在一些受体动物组中减弱了促甲状腺激素(TSH)介导的肿瘤促进强度。我们发现,血清TSH水平较高的大鼠与TSH水平较低的大鼠相比,辐射相关癌症的发病率显著更高。我们从这些数据中得出结论:(1)放射性甲状腺癌发生率很高;(2)慢性TSH刺激加速放射性肿瘤向明显癌的进展,并促进未照射甲状腺克隆原移植中晚期出现癌症的发生。

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