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循环细胞外囊泡 DNA 中检测到的 TP53 突变与肝细胞癌患者的预后相关。

TP53 mutation detected in circulating exosomal DNA is associated with prognosis of patients with hepatocellular carcinoma.

机构信息

Department of Hepatobiliary and Pancreatic Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang, China.

Department of Hepatobiliary and Pancreatic Surgery, Jiangxi Provincial People's Hospital, Nanchang, China.

出版信息

Cancer Biol Ther. 2022 Dec 31;23(1):439-445. doi: 10.1080/15384047.2022.2094666.

Abstract

Exosome DNA (exoDNA) can be used for liquid biopsy. This study was the first to use droplet digital PCR (ddPCR) to detect tumor-specific mutations in exoDNA and to evaluate the prognosis of hepatocellular carcinoma (HCC) patients. 60 HCC patients were enrolled in the study. We used ddPCR to detect c.747 G > T mutation in TP53 gene. We analyzed the correlation between detectable mutation in exoDNA and clinicopathologic characteristics using Multivariate logistics regression analysis. We performed Cox regression to assess the correlation between mutation frequency (mutant droplets/total droplets, MD/TD) and prognostic. We found that 48 of 60 patients had c.747 G > T mutation in TP53 gene in exoDNA (80.0%). We found that detectable mutation in exoDNA and age were associated with microvascular invasion (MVI) (P < .01). The ROC curve analysis revealed that the best cutoff value of mutation frequency to predict MVI was 67% (sensitivity 48.15%, specificity 93.94%,), the corresponding AUC was 0.761 (95%CI, 0.640-0.866; P < .01). Furthermore, we found that patients suffered high-frequency mutation (>67%) had shorted median recurrence-free survival (RFS) with 63 days (range, 53-202 days), compared with 368 days (range, 51-576 days) for patients with low-frequency mutation (<67%) (HR:4.61; 95% CI, 1.70-12.48; P = 0 .003). We also found that high-frequency mutation was associated with poor prognosis though patients had better pathological characteristics, such as AFP (<400 ng/mL), Liver cirrhosis (Negative), Tumor thrombus (Negative), Tumor numbers (Single) and Post-operation TACE (Executed). We provided evidence that the mutations in exoDNA might be used to predict patients with poor RFS. TP53: Tumor protein p53; ExoDNA: Exosomal DNA; HCC: Hepatocellular carcinoma; ddPCR: Droplet digital Polymerase Chain Reaction (PCR); MD/TD: The ratio of mutant droplets/total droplets; AFP: Alpha-fetoprotein; MVI: Microvascular invasion; RFS: Recurrence-free survival.

摘要

外泌体 DNA(exoDNA)可用于液体活检。本研究首次使用液滴数字 PCR(ddPCR)检测外泌体中的肿瘤特异性突变,并评估肝癌(HCC)患者的预后。共纳入 60 例 HCC 患者。我们使用 ddPCR 检测 TP53 基因中的 c.747 G > T 突变。采用多因素逻辑回归分析,分析外泌体中可检测到的突变与临床病理特征的相关性。采用 Cox 回归评估突变频率(突变液滴/总液滴,MD/TD)与预后的相关性。结果发现,60 例患者中有 48 例(80.0%)在 exoDNA 中存在 TP53 基因 c.747 G > T 突变。我们发现,外泌体中可检测到的突变和年龄与微血管侵犯(MVI)相关(P <.01)。ROC 曲线分析显示,突变频率预测 MVI 的最佳截断值为 67%(灵敏度 48.15%,特异性 93.94%),相应 AUC 为 0.761(95%CI,0.640-0.866;P <.01)。此外,我们发现高频突变(>67%)患者的中位无复发生存期(RFS)较短,为 63 天(范围为 53-202 天),而低频突变(<67%)患者的 RFS 为 368 天(范围为 51-576 天)(HR:4.61;95%CI,1.70-12.48;P =.003)。我们还发现,尽管高频突变患者具有更好的病理特征,如 AFP(<400ng/mL)、肝硬化(阴性)、肿瘤血栓(阴性)、肿瘤数量(单发)和术后 TACE(执行),但高频突变与不良预后相关。我们提供的证据表明,外泌体中的突变可用于预测 RFS 较差的患者。TP53:肿瘤蛋白 p53;ExoDNA:外泌体 DNA;HCC:肝细胞癌;ddPCR:液滴数字聚合酶链反应(PCR);MD/TD:突变液滴/总液滴的比值;AFP:甲胎蛋白;MVI:微血管侵犯;RFS:无复发生存期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec0d/9354767/84fc614b7c6b/KCBT_A_2094666_F0001_OC.jpg

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