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脑胶质瘤患者中丙酮酸激酶 M2(PKM-2)的表达及其预后意义。

Pyruvate kinase M2 (PKM-2) expression and prognostic significance in glioblastoma patients.

机构信息

Department of Radiation Oncology, Meram Medical School, Necmettin Erbakan University, Konya, Turkey.

Department of Pathology, Meram Medical School, Necmettin Erbakan University, Konya, Turkey.

出版信息

J Neurooncol. 2023 Dec;165(3):527-533. doi: 10.1007/s11060-023-04521-1. Epub 2023 Nov 27.

Abstract

PURPOSE

Pyruvate kinase M2 (PKM2) is a key enzyme that catalyzes the irreversible and final step of glycolysis. It is closely associated with cancer development and progression. The relationship between PKM2 and prognosis in glioblastoma (GB) patients is unknown. The aim of this study was to measure PKM2 expression and evaluate its effect on prognosis in GB patients.

METHODS

Patients who underwent radiotherapy (RT) for glioblastoma between 2010 and 2021 were evaluated immunohistochemically. A single pathologist evaluated pathology specimens of all patients. The intensity and extent of staining of tumor cells were scored. Patients were categorized as low and high PKM2.

RESULTS

A total of 119 patients were evaluated. While 80.7% of the cases had a low score, 19.3% had a high PKM2 score. It was observed that the group with high PKM2 expression had lower performance, received more hypofractionated RT and received adjuvant chemotherapy (CT) less frequently. Median overall survival (OS) was 15.77 months in the low PKM2 expression group and 6.50 months in the high PKM2 group. In univariate analyses, PKM2 expression, age, performance status, type of surgery, RT scheme, and concurrent and adjuvant CT were prognostic factors in predicting OS. In multivariate analyses, PKM2 expression, type of surgery, RT scheme and receiving adjuvant CT were prognostic factors for OS.

CONCLUSION

PKM2 is an independent prognostic factor for survival and is associated with poor prognosis in GBM patients treated with radiotherapy. It may be a potential therapeutic target for anticancer therapy.

摘要

目的

丙酮酸激酶 M2(PKM2)是一种关键酶,可催化糖酵解的不可逆和终末步骤。它与癌症的发展和进展密切相关。PKM2 与胶质母细胞瘤(GB)患者预后的关系尚不清楚。本研究旨在测量 PKM2 的表达,并评估其对 GB 患者预后的影响。

方法

评估了 2010 年至 2021 年间接受放疗(RT)的胶质母细胞瘤患者的免疫组织化学。一位单独的病理学家评估了所有患者的病理标本。对肿瘤细胞的染色强度和范围进行评分。患者被分为低 PKM2 和高 PKM2。

结果

共评估了 119 例患者。虽然 80.7%的病例评分较低,但有 19.3%的病例 PKM2 评分较高。观察到高 PKM2 表达组的表现较低,接受了更多的低分割 RT,并且较少接受辅助化疗(CT)。低 PKM2 表达组的中位总生存期(OS)为 15.77 个月,高 PKM2 组为 6.50 个月。在单因素分析中,PKM2 表达、年龄、表现状态、手术类型、RT 方案以及同期和辅助 CT 是预测 OS 的预后因素。在多因素分析中,PKM2 表达、手术类型、RT 方案和接受辅助 CT 是 OS 的预后因素。

结论

PKM2 是生存的独立预后因素,与接受放疗的 GBM 患者的不良预后相关。它可能是抗癌治疗的潜在治疗靶点。

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