Carcinogenic Interactions of Radiation and Chemicals

我们之前证明了敏感的BALB/cByJ和耐药的C57BL/6ByJ小鼠对辐射诱导的乳腺癌的易感性和辐射诱导的细胞遗传不稳定性的品系差异，并提供了这种易感性差异是遗传性状的证据。对这些菌株的cDNA序列分析表明，BALB/c小鼠具有两种独特的多态性。对两种菌株、F1杂交种和回交动物的研究表明，对辐射诱导的细胞遗传不稳定性的易感性与Prkdc （DNA依赖性蛋白激酶催化亚基的编码基因PKcs）之间存在显著关联。BALB/c Prkdc等位基因（Prkdc BALs’c）纯合的小鼠也缺乏辐照后双链断裂的修复，显示出激酶活性降低，western分析显示DNA-PKcs信号强度降低。由于修复缺陷、western信号强度降低、激酶活性降低以及这两种多态性的存在都与辐射诱导的细胞遗传不稳定性易感性增加显著相关，我们现在建议研究该位点与辐射诱导的乳腺癌易感性之间的遗传联系，并更直接地阐明Prkdc BALB/cin辐射诱导的不稳定性和乳腺癌的作用。我们现在也证明了来自BALB/c和SCID的乳腺细胞，它们具有Prkdc的截断突变，辐射导致端粒之间的融合和辐射诱导的双链断裂（DSB），这可能是由于DNA- PKcs作为端粒维持的重要元素的功能缺陷造成的。具体来说，该项目的目的是：1)直接确定PrkdcBALB多态性的功能后果；2)确定Prkdc BALB在辐射诱发乳腺癌易感性中的作用；3)确定端粒功能障碍在辐射诱导的细胞遗传不稳定和乳腺癌中的作用。网站性能 ======================================== 节结束 ===========================================

EXCEED THE SPACE We previously demonstrated strain differences in susceptibility to radiation-induced mammary cancer and radiation- induced cytogenetic instability between sensitive BALB/cByJ, and resistant C57BL/6ByJ mice and provided evidence that such susceptibility differences were heritable traits. Sequence analysis of cDNA from these strains indicate two polymorphisms unique to the BALB/c mouse. Studies in the two strains, F1 hybrids, and in backcross animals have demonstrated a significant association between susceptibility to radiation-induced cytogenetic instability and Prkdc, the gene encoding the catalytic subunit of DNA dependent protein kinase (DNA PKcs). Mice homozygous for the BALB/c Prkdc allele (Prkdc BALs'c) are also deficient in the post-irradiation repair of double strand breaks, showed a reduced kinase activity, and western analyses showed a reduced intensity of signal for DNA-PKcs. Since the repair deficiency, reduced western signal intensity, reduced kinase activity, and the presence of these two polymorphisms are all significantly associated with increased susceptibility to radiation-induced cytogenetic instability, we now propose to examine the genetic linkage between this locus and susceptibility to radiation-induced mammary cancer, and to more directly illucidate the role of Prkdc BALB/cin radiation-induced instability and mammary cancer. We have now also demonstrated that irradiation of mammary cells from BALB/c as well as SCID, which have a truncating mutation of Prkdc, results in fusions between telomeres and radiation-induced double strand breaks (DSB) presumably as a result of a defect in the function of DNA- PKcs as an important element in telomere maintenance. Specifically, the aims of this project are to: 1) directly determine the functional consequence of polymorphorisms in PrkdcBALB; 2) determine the role of Prkdc BALB in susceptibility to radiation-induced mammary cancer; 3) determine the contribution of telomere dysfunction in radiation-induced cytogenetic instability and mammary cancer. PERFORMANCE SITE ========================================Section End===========================================