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Prognostic value of aberrant hypermethylation in pleural effusion of lung adenocarcinoma

机译:甲基化异常在肺腺癌胸腔积液中的预后价值

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摘要

Lung adenocarcinoma is one of the most frequent causes of malignant pleural effusions (MPE ). The presence of MPE bears a poor prognosis. Although epigenetic changes are commonly related to human neoplasia, scarce date is available on patients with MPE . We aimed to estimate the prognostic value of DNA methylation of tumor suppressor genes from pleural fluid. Thirty patients with MPE due to lung adenocarcinoma were prospectively included. Methylation-specific (MS) PCR was used to study the methylation status of the promoter region of tumor suppressor genes p16/INK4a, MGMT, BRCA1 and RARβ in pleural fluid. Clinical data and survival were collected. Survival analysis was performed using Kaplan-Meier plots and Cox regression. Hypermethylation in at least one gene was detected in 25 patients (83.3%). On multivariate analysis factors significantly associated with shorter survival were the lack of hypermethylation in any of the studied genes (hazard ratio = 9.3; p = 0.001), Charlson index ≥ 3 (hazard ratio = 9.6, p = 0.002) and no oncological treatment (hazard ratio = 11.1; p < 0.001). Analysis of aberrant promoter hypermethylation of tumor suppressor genes may be useful in predicting prognosis, but further studies are needed to validate our findings.
机译:肺腺癌是恶性胸腔积液(MPE)的最常见原因之一。 MPE的存在预后不良。尽管表观遗传学改变通常与人类瘤形成有关,但MPE患者的病因稀少。我们旨在评估胸膜液中抑癌基因DNA甲基化的预后价值。前瞻性纳入了30例因肺腺癌引起的MPE患者。甲基化特异性(MS)PCR用于研究胸水中抑癌基因p16 / INK4a,MGMT,BRCA1和RARβ的启动子区域的甲基化状态。收集临床数据和生存率。使用Kaplan-Meier图和Cox回归进行生存分析。在25例患者中检测到至少一个基因的甲基化过高(83.3%)。在与较短生存期显着相关的多元分析因素上,任何研究的基因均缺乏高甲基化(危险比= 9.3; p = 0.001),查尔森指数≥3(危险比= 9.6,p = 0.002)和未进行肿瘤治疗(危险比= 11.1; p <0.001)。肿瘤抑制基因异常启动子甲基化的分析可能有助于预测预后,但是需要进一步的研究来验证我们的发现。

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