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Prognostic value of indoleamine 2,3-dioxygenase expression in high grade osteosarcoma

机译:吲哚胺2,3-双加氧酶表达在高级骨肉瘤中的预后价值

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摘要

Indoleamine 2,3-dioxygenase (IDO) is a tryptophan-catabolising enzyme inducing immune tolerance. Some reports have noted a clinical correlation between IDO expression and outcome in some malignant tumors. This study aimed to investigate IDO expression as related to prognosis in osteosarcoma. IDO expression was immunohistochemically scored as five grades. IDO was expressed in most of the cases. Univariate analysis revealed no significant correlation between IDO staining intensity and various variables including sex, age, anatomical site, chemotherapy regimen, necrosis after chemotherapy, and surgical stage. Patients with high IDO expression had significantly lower metastasis-free survival (P = 0.016) and overall survival (P = 0.005). On univariate analysis, age over 20 years and high IDO expression were found to be independent risk factors of lower overall survival and metastasis-free survival. On multivariate analysis, there was no significant correlation between high IDO expression and metastasis-free survival (P = 0.070) and overall survival (P = 0.066). The immune tolerance mediated through IDO may have an important role in the tumorigenesis of osteosarcoma and may exert an impact on the clinical outcome, and thus may lend itself as a therapeutic target of immunotherapy for osteosarcoma.
机译:吲哚胺2,3-二加氧酶(IDO)是一种色氨酸分解酶,可诱导免疫耐受。一些报告指出了IDO表达与某些恶性肿瘤的预后之间的临床相关性。这项研究旨在调查与骨肉瘤预后相关的IDO表达。免疫组织化学IDO的表达分为五个等级。在大多数情况下都表示有IDO。单因素分析显示IDO染色强度与各种变量之间无显着相关性,这些变量包括性别,年龄,解剖部位,化疗方案,化疗后坏死和手术阶段。 IDO表达高的患者的无转移生存期(P = 0.016)和总生存期(P = 0.005)明显较低。在单因素分析中,发现20岁以上的年龄和较高的IDO表达是降低总生存率和无转移生存率的独立危险因素。在多变量分析中,高IDO表达与无转移生存期(P = 0.070)和总生存期(P = 0.066)之间没有显着相关性。通过IDO介导的免疫耐受可能在骨肉瘤的肿瘤发生中起重要作用,并且可能对临床结果产生影响,因此可以作为骨肉瘤免疫治疗的治疗目标。

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