肿瘤放疗患者的磷酸化P53 (TP53

Amna A. Ali, O. Abdalla, Nuha M. Hassan, Amna A. Yousif, Ammar ME. Hassan, Alkhansa Mahmoud
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摘要

癌症是世界范围内的一种常见疾病,放射治疗是癌症治疗的重要选择。P53肿瘤抑制因子在细胞凋亡和肿瘤治疗反应中起作用。在电离辐射的作用下,共济失调毛细血管扩张突变家族(ATM)的激酶会使P53磷酸化。本研究的目的是通过测量T18上磷酸化P53的表达水平,检测放射治疗前后癌症患者的DND损伤反应。材料与方法:本研究选取28例接受放疗的癌症患者,在放疗前后采集血液样本,并与28例年龄、性别匹配的健康人作为对照组。采用酶联免疫吸附法(ELISA)从CUSABIO获得P53抗体(T18)。结果:乳腺癌21例,头颈部7例,男性6例,女性22例。年龄中位数为44岁。乳腺癌患者的身体质量指数(BMI)中位数为30,头颈部患者的BMI中位数为23。乳腺癌的吸收剂量为40.5Gy。而头颈癌的剂量在20Gy- 66Gy之间。与对照组相比,放疗前患者磷酸化P53表达显著升高(P= <0.0001)。而放疗前组和放疗后组无显著差异(P=0.7)。个别患者放疗后P53磷酸化表达升高19例,放疗后P53低表达9例,其中8例诊断为乳腺癌,1例诊断为食道癌。结论:T18磷酸化可作为癌症的预测指标。磷酸化的P53可通过其激活和促凋亡作用来指示DNA损伤和应答。P53等蛋白表达可作为癌症患者个体放射敏感性的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phosphorylated P53 (TP53) in Cancer Patients Undergoing Radiotherapy
Introduction: Cancer is a common disease worldwide, and radiotherapy is an important option for cancer treatment. P53 tumour suppressor has a role in apoptosis and cancer treatment response. P53 is phosphorylated in response to ionizing radiation by kinases of the ataxia telangiectasia mutation family (ATM). The aim of this study was to detect the DND damage response in cancer patients before and after radiation therapy through measurements the expression levels of phosphorylated P53 on T18. Material and Methods: Total of 28 cancer patients on radiotherapy were participate in this study to collect blood samples pre and post radiotherapy compared to 28 healthy people matched in age and sex as control group. P53 antibody used against Phospho-p53 (T18) was obtained from CUSABIO using enzyme linked immunosorbent assay (ELISA). Results: 21 of patients were breast cancer, and 7 of patients were Head and Neck. 6 male and 22 female. Median of age was 44 years old. Median of body mass index (BMI) for breast cancer patients was 30 while BMI for head and neck was 23. The absorbed dose for breast cancer was 40.5Gy. While the doses for Head and neck cancers were between 20Gy- 66Gy. Phosphorylated P53 expression increased significantly (P= <0.0001) in the patients preradiotherapy compared to the control group. While no significant difference observed between preradiotherapy and postradiotherapy groups (P=0.7). Individually, 19 patients showed increased in phosphorylated P53 expression postradiotherapy, while, nine patients were showed low P53 postradiotherapy, 8 of them diagnosed with breast cancer and 1 diagnosed with Oesophagus. Conclusion: phosphorylated on T18 can be consider a predictive marker for cancer. Phosphorylated P53 can be indict the DNA damage and response through its activation and proapoptotic effects. Protein expression such as P53 can be use as biomarker to demonstrate individual radiation sensitivity in cancer patients.
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