Kennedy Ann R, Maity Amit, Sanzari Jenine K
Department of Radiation Oncology Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Radiat Res. 2016 Aug;186(2):121-40. doi: 10.1667/RR14406.1. Epub 2016 Jul 26.
Results from our recent studies have led to the novel hypothesis that radiation-induced coagulopathy (RIC) and associated hemorrhage occurring as part of the acute radiation syndrome (ARS) is a major cause of death resulting from radiation exposure in large mammals, including humans. This article contains information related to RIC, as well as potential strategies for the prevention and treatment of RIC. In addition, new findings are reported here on the occurrence of RIC biomarkers in humans exposed to radiation. To determine whether irradiated humans have RIC biomarkers, blood samples were obtained from radiotherapy patients who received treatment for different types of malignancies. Blood samples from allogeneic hematopoietic cell transplantation (allo-HCT) patients obtained before, during and after irradiation indicated that exposure led to prolonged clot formation times, increased levels of thrombin-antithrombin III (TAT) complex and increased circulating nucleosome/histone (cNH) levels, which suggest potential coagulopathies in the allo-HCT patients. Since these allo-HCT patients received chemotherapy prior to radiotherapy, it is possible that the chemical agents could have influenced the observed results. Frozen plasma samples from radiotherapy patients with prostate, lung and breast cancer were also obtained for analyses of cNH levels. The results indicated that some of these patients had very high cNH blood levels. Analysis of cNH levels in plasma samples from irradiated ferrets also indicated increased cNH levels compared to preirradiation baseline levels. The results from irradiated animals and some radiotherapy patients suggest the possibility that anti-histone antibodies, which block the toxic effects of elevated cNH levels in the blood, might be useful as therapeutic agents for adverse biological radiation-induced effects. The detection of increased levels of cNH in some radiotherapy patient blood samples demonstrates its potential as a biomarker for diagnosing and/or predicting the propensity for developing coagulopathies/hemorrhage, offering possible treatment options with personalized medicine therapies for cancer patients.
我们近期研究的结果引出了一个新的假说,即作为急性放射综合征(ARS)一部分的辐射诱导凝血病(RIC)及相关出血是包括人类在内的大型哺乳动物因辐射暴露导致死亡的主要原因。本文包含了与RIC相关的信息,以及预防和治疗RIC的潜在策略。此外,本文还报告了辐射暴露人类中RIC生物标志物出现情况的新发现。为了确定受辐照人类是否有RIC生物标志物,我们从接受不同类型恶性肿瘤治疗的放疗患者身上采集了血样。同种异体造血细胞移植(allo-HCT)患者在辐照前、辐照期间和辐照后的血样表明,辐射暴露导致凝血形成时间延长、凝血酶 - 抗凝血酶III(TAT)复合物水平升高以及循环核小体/组蛋白(cNH)水平升高,这表明allo-HCT患者存在潜在的凝血病。由于这些allo-HCT患者在放疗前接受了化疗,化学药物有可能影响了观察结果。我们还获取了前列腺癌、肺癌和乳腺癌放疗患者的冷冻血浆样本,用于分析cNH水平。结果表明,其中一些患者的cNH血液水平非常高。对辐照雪貂血浆样本中cNH水平的分析也表明,与辐照前基线水平相比,cNH水平有所升高。辐照动物和一些放疗患者的结果表明,能够阻断血液中升高的cNH水平毒性作用的抗组蛋白抗体,可能作为治疗辐射诱导不良生物学效应的药物。在一些放疗患者血样中检测到cNH水平升高,证明了其作为诊断和/或预测凝血病/出血倾向生物标志物的潜力,为癌症患者提供了个性化药物治疗的可能选择。