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Expression and clinical significance of the phosphatidylinositol 3-kinase/protein kinase B signal transduction pathway in non-small cell lung carcinoma

机译:磷脂酰肌醇3-激酶/蛋白激酶B信号转导通路在非小细胞肺癌中的表达及其临床意义

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摘要

The overactivation of the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) signal transduction pathway has been examined in various carcinomas and is reported to be significantly correlated with prognosis. However, little is known with regard to the PI3K/Akt signal transduction pathway in advanced non-small cell lung carcinoma (NSCLC). The present study investigated the expression of PI3K and phosphorylated (p)-Akt protein and its clinical significance in NSCLC. The clinical records of 157 patients with NSCLC (70 stage I–IIIA and 87 stage IIIB–IV cases), consisting of 75 cases of squamous cell carcinoma and 82 cases of adenocarcinoma, together with 30 resected lung cancer tumor-adjacent tissue samples, were retrospectively evaluated. PI3K and p-Akt expression in the NSCLC and tumor-adjacent tissues were measured using an immunohistochemical method, and its correlation with the clinicopathological data and prognosis in advanced NSCLC was evaluated. PI3K and p-Akt expression was significantly higher in the cancer tissues (χ2=14.8455; P=0.001) than in the tumor-adjacent tissues (χ2=14.2615; P=0.001). The overexpression of p-Akt in stage I–IIIA NSCLC was associated with lymph node metastasis (χ2=6.1189; P=0.013) and tumor-node-metastasis (TNM) stage (χ2=8.9752; P=0.011), however, no correlation was observed with gender, age, pathological type and histological grade. The overexpression of p-Akt in stage IIIB–IV NSCLC was only associated with TNM stage (χ2=5.7501; P=0.016), and no correlation was observed with gender, age, pathological type, histological grade and Eastern Cooperative Oncology Group (ECOG) performance status (PS). The overexpression of PI3K was not found to correlate with the aforementioned clinicopathological variables in all patients. Survival was significantly improved in advanced NSCLC with PI3K- and p-Akt-negative expression compared with PI3K- and p-Akt-positive expression [P13K: 17.70 months (95% confidence interval (CI), 15.11–20.28 months) vs. 13.43 months (95% CI, 11.83–15.02 months); P=0.004; and p-Akt: 17.13 months (95% CI, 14.93–19.34 months) vs. 13.07 months (95% CI, 11.32–14.82 months); P=0.007]. Multivariate analysis showed that PI3K [hazard ratio (HR)=2.143; 95% CI, 1.211–3.790; P=0.009], p-Akt (HR=1.991; 95% CI, 1.009–3.927; P=0.047), TNM stage (HR=4.788; 95% CI, 2.591–8.848; P=0.001) and ECOG-PS (HR=3.272; 95% CI, 1.701–6.296; P=0.001) were independent predictors for survival in stage IIIB–IV NSCLC. These results indicated that p-Akt overexpression closely correlates with factors of an unfavorable prognosis in NSCLC. PI3K and p-Akt overexpression are independent markers of a poor prognosis in advanced NSCLC.
机译:磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(Akt)信号转导通路的过度激活已在各种癌症中进行了检查,并据报道与预后显着相关。然而,关于晚期非小细胞肺癌(NSCLC)中PI3K / Akt信号转导途径的了解甚少。本研究调查了PI3K和磷酸化(p)-Akt蛋白在NSCLC中的表达及其临床意义。记录了157例NSCLC患者的临床记录(70例I–IIIA期和87例IIIB–IV期),包括75例鳞状细胞癌和82例腺癌,以及30例切除的肺癌肿瘤附近组织样本。回顾性评估。用免疫组织化学方法检测非小细胞肺癌和癌旁组织中PI3K和p-Akt的表达,并评估其与晚期非小细胞肺癌临床病理资料和预后的关系。癌组织中的PI3K和p-Akt表达(χ 2 = 14.8455; P = 0.001)显着高于癌旁组织(χ 2 = 14.2615; P <0.001)。 P = 0.001)。 I–IIIA期非小细胞肺癌中p-Akt的过度表达与淋巴结转移(χ 2 = 6.1189; P = 0.013)和肿瘤-淋巴结转移(TNM)期有关(χ 2 = 8.9752; P = 0.011),但与性别,年龄,病理类型和组织学分级无相关性。 IIIB–IV期非小细胞肺癌中p-Akt的过度表达仅与TNM分期有关(χ 2 = 5.7501; P = 0.016),与性别,年龄,病理类型,组织学无相关性。年级和东部合作肿瘤小组(ECOG)的表现状态(PS)。在所有患者中均未发现PI3K的过表达与上述临床病理变量相关。与PI3K和p-Akt阳性表达相比,PI3K和p-Akt阴性表达的晚期NSCLC患者的生存率显着提高[P13K:17.70个月(95%置信区间(CI),15.11–20.28个月),相对于13.43。个月(95%CI,11.83–15.02个月); P = 0.004;和p-Akt:17.13个月(95%CI,14.93-19.34个月)与13.07个月(95%CI,11.32-14.82个月); P = 0.007]。多因素分析表明,PI3K [危险比(HR)= 2.143; 95%CI,1.211–3.790; P = 0.009],p-Akt(HR = 1.991; 95%CI,1.009–3.927; P = 0.047),TNM分期(HR = 4.788; 95%CI,2.591–8.848; P = 0.001)和ECOG-PS( HR = 3.272; 95%CI,1.701-6.296; P = 0.001)是IIIB-IV期NSCLC生存的独立预测因子。这些结果表明,p-Akt的过度表达与NSCLC预后不良的因素密切相关。 PI3K和p-Akt过表达是晚期NSCLC预后不良的独立标志。

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