Zhao Junsheng, Hu Zekai, Zheng Xiaoping, Lin Yajie, Liu Xiao, Zhang Junjie, Peng Jing, Gao Hainv
Key Laboratory of Artificial Organs and Computational Medicine in Zhejiang Province, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, China.
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Front Cell Dev Biol. 2024 Nov 22;12:1489836. doi: 10.3389/fcell.2024.1489836. eCollection 2024.
Hepatocellular Carcinoma (HCC) is a malignant tumor with high morbidity and mortality worldwide, which represents a serious threat to human life, health and quality of life. Blood-based detection is essential for HCC screening, early diagnosis, prognosis evaluation, and surveillance. Current non-invasive detection strategy including serum alpha-fetoprotein (AFP), ultrasound, computerized tomography, and magnetic resonance imaging. The limited specificity of an AFP and the dependence on operator experience and diagnostic personnel for ultrasound have constrained their utility in early HCC diagnosis. In recent years, with the development of various detection technologies, there has been an increasing focus on exploring blood-based detection markers for HCC. The types of markers include protein markers, DNA mutation, DNA epigenetic modification, mRNA, miRNA, and so on. However, numerous methodological and biological factors limit the clinical sensitivity and generalization performance of these new biomarkers. In this review, we describe the state-of-the-art technologies for cfDNA analysis, and discuss outstanding biological and technical challenges that, if addressed, would substantially improve HCC diagnostics and patient care.
肝细胞癌(HCC)是一种在全球范围内发病率和死亡率都很高的恶性肿瘤,对人类生命、健康和生活质量构成严重威胁。基于血液的检测对于HCC筛查、早期诊断、预后评估和监测至关重要。当前的非侵入性检测策略包括血清甲胎蛋白(AFP)、超声、计算机断层扫描和磁共振成像。AFP的特异性有限,以及超声对操作者经验和诊断人员的依赖,限制了它们在早期HCC诊断中的应用。近年来,随着各种检测技术的发展,人们越来越关注探索基于血液的HCC检测标志物。标志物类型包括蛋白质标志物、DNA突变、DNA表观遗传修饰、mRNA、miRNA等。然而,众多方法学和生物学因素限制了这些新生物标志物的临床敏感性和推广性能。在本综述中,我们描述了用于游离DNA分析的最新技术,并讨论了一些突出的生物学和技术挑战,如果这些挑战能够得到解决,将显著改善HCC诊断和患者护理。