外周血单核细胞 DNA 甲基化标记的临床验证,用于准确早期检测亚洲患者的肝细胞癌。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
David Cheishvili, Chifat Wong, Mohammad Mahbubul Karim, Mohammad Golam Kibria, Nusrat Jahan, Pappu Chandra Das, Abul Khair Yousuf, Atikul Islam, Dulal Chandra Das, Sheikh Mohammad Noor-E-Alam, Sarwar Alam, Mustafizur Rahman, Wasif A. Khan, Mamun Al-Mahtab, Moshe Szyf
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引用次数: 0

摘要

背景:肝细胞癌(HCC)是全球癌症相关死亡的主要原因,其早期检测面临巨大挑战。提高诊断的准确性可以极大地影响患者的预后,这就强调了对创新性、非侵入性生物标志物的需求:本研究利用一组 402 名参与者(包括健康对照组、慢性肝炎患者和来自孟加拉国的 HCC 患者)来评估外周血单核细胞(PBMC)中的 DNA 甲基化特征。我们对之前确定的选定基因进行了有针对性的新一代测序,以评估其甲基化动态。根据这些动态变化制定了 M8 和 M4 评分,并使用接收者操作特征(ROC)分析来确定它们在检测早期 HCC 方面的有效性,以及现有标记物(如表肝和甲胎蛋白(AFP))的有效性:结果:将M8和M4评分与肝外周血和甲胎蛋白结合可显著提高早期HCC的诊断灵敏度。M4+epiLiver 评分在 A 期 HCC 中的灵敏度为 79.4%,而将 M4 与 AFP 结合可将所有阶段的灵敏度提高到 88.2-95.7%,这表明与单独使用每个标记物相比,M4+epiLiver 评分的诊断性能更优:我们的研究证实,将基因甲基化图谱与已确立的诊断标记物相结合可大幅提高检测早期 HCC 的灵敏度。这种综合诊断方法有望推动无创癌症诊断的发展,并有可能导致更早的治疗干预和提高高危患者的生存率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical validation of peripheral blood mononuclear cell DNA methylation markers for accurate early detection of hepatocellular carcinoma in Asian patients

Clinical validation of peripheral blood mononuclear cell DNA methylation markers for accurate early detection of hepatocellular carcinoma in Asian patients
Hepatocellular carcinoma (HCC), a leading cause of cancer-related deaths globally, poses significant challenges in early detection. Improved diagnostic accuracy can drastically influence patient outcomes, emphasizing the need for innovative, non-invasive biomarkers. This study utilized a cohort of 402 participants, including healthy controls, chronic hepatitis patients, and HCC patients from Bangladesh, to evaluate DNA methylation signatures in peripheral blood mononuclear cells (PBMC). We performed targeted next-generation sequencing on selected genes previously identified to assess their methylation dynamics. The development of M8 and M4 scores was based on these dynamics, using Receiver Operating Characteristic (ROC) analysis to determine their effectiveness in detecting early-stage HCC alongside existing markers such as epiLiver and alpha-fetoprotein (AFP). Integration of M8 and M4 scores with epiLiver and AFP significantly enhances diagnostic sensitivity for early-stage HCC. The M4+epiLiver score achieves a sensitivity of 79.4% in Stage A HCC, while combining M4 with AFP increases sensitivity to 88.2–95.7% across all stages, indicating a superior diagnostic performance compared to each marker used alone. Our study confirms that combining gene methylation profiles with established diagnostic markers substantially improves the sensitivity of detecting early-stage HCC. This integrated diagnostic approach holds promise for advancing non-invasive cancer diagnostics, potentially leading to earlier treatment interventions and improved survival rates for high-risk patients. Cheishvili et al. investigate the use of DNA methylation markers in peripheral blood mononuclear cells for early detection of hepatocellular carcinoma in an Asian cohort. The study demonstrates that these biomarkers can accurately distinguish between healthy controls and patients across different stages of the disease. Liver cancer is one of the top causes of cancer death worldwide, and finding it early is crucial for successful treatment. This research focuses on using a simple blood test to look for specific DNA changes that signal the early stages of liver cancer. We tested this method on a diverse group of people from Bangladesh, including those already at high risk for liver cancer due to chronic liver infections. By combining this new blood test with other existing tests, we were able to detect liver cancer more accurately and earlier than by using traditional methods alone. This approach could make it easier and less invasive to find liver cancer early, offering a better chance for effective treatment and a hopeful prognosis for those at risk.
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