首页> 外文期刊>European journal of oral sciences >Expression and prognostic significance of the P53‐related DNA damage repair proteins checkpoint kinase 1 (CHK1) and growth arrest and DNA‐damage‐inducible 45 alpha (GADD45A) in human oral squamous cell carcinoma
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Expression and prognostic significance of the P53‐related DNA damage repair proteins checkpoint kinase 1 (CHK1) and growth arrest and DNA‐damage‐inducible 45 alpha (GADD45A) in human oral squamous cell carcinoma

机译:P53相关DNA损伤修复蛋白检查点激酶1(CHK1)和生长停滞和DNA损伤诱导45α(GADD45A)在人口鳞状细胞癌中的表达及预后意义

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摘要

DNA damage repair is a key factor in the maintenance of cell genome stability, plays an important role in the regulation of tumour evolution, and can affect the prognosis of cancer patients. This study aimed to detect the protein expression of the DNA damage repair protein P53 and its upstream and downstream regulators, CHK1, GADD45A, and MDM2, in oral squamous cell carcinoma (OSCC), in order to analyse the association between the expression of these proteins and overall survival, and to assess their prognostic implications for OSCC patients. The expression of the above proteins was detected by immunohistochemistry in 80 human OSCC tissue samples and in non‐cancerous tissue samples. Compared to that in the non‐cancerous tissue, the expression of CHK1, GADD45A, and MDM2 in OSCC tissue was significantly increased. The protein expression of the tumour suppressor gene P53 was also increased. Patients with high CHK1 and MDM2 expression levels had a reduced survival time and a poor prognosis, whereas patients with high GADD45A expression levels had a good prognosis. Our results indicate that high CHK1 expression is an independent risk factor for poor OSCC prognosis, and that CHK1 may be a potential target for OSCC clinical treatment.
机译:DNA损伤修复是维持细胞基因组稳定性的关键因素,在肿瘤进化调节中起重要作用,并可能影响癌症患者的预后。本研究旨在检测口腔鳞状细胞癌(OSCC)中DNA损伤修复蛋白P53及其上游和下游调节剂,CHK1,GADD45A和MDM2的蛋白质表达,以分析这些蛋白质表达之间的关联和整体生存,并评估其对OSCC患者的预后影响。通过免疫组织化学在80人OSCC组织样品和非癌组织样品中检测上述蛋白质的表达。与非癌组织中的表达相比,OSCC组织中CHK1,GADD45A和MDM2的表达显着增加。肿瘤抑制基因P53的蛋白质表达也增加。 HIGK1和MDM2表达水平的患者减少了生存时间和预后差,而高态度的表达水平患者具有良好的预后。我们的结果表明,高CHK1表达是OSCC预后不良的独立危险因素,并且CHK1可能是OSCC临床治疗的潜在目标。

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