Rashid Sana, Sun Yingchuan, Ali Khan Saddozai Umair, Hayyat Sikandar, Munir Muhammad Usman, Akbar Muhammad Usman, Khawar Muhammad Babar, Ren Zhiguang, Ji Xinying, Ihsan Ullah Khan Malik
Institute of Molecular Biology and Biotechnology, University of Lahore, Lahore 54590, Pakistan.
Department of Internal Oncology (Section I), Xuchang Municipal Central Hospital, Xuchang 461000, China.
Chin J Cancer Res. 2024 Apr 30;36(2):195-214. doi: 10.21147/j.issn.1000-9604.2024.02.07.
Hepatocellular carcinoma (HCC) is considered the fifth most prevalent cancer among all types of cancers and has the third most morbidity value. It has the most frequent duplication time and a high recurrence rate. Recently, the most unique technique used is liquid biopsies, which carry many markers; the most prominent is circulating tumor DNA (ctDNA). Varied methods are used to investigate ctDNA, including various forms of polymerase chain reaction (PCR) [emulsion PCR (ePCR), digital PCR (dPCR), and bead, emulsion, amplification, magnetic (BEAMing) PCR]. Hence ctDNA is being recognized as a potential biomarker that permits early cancer detection, treatment monitoring, and predictive data on tumor burden are subjective to therapy or surgery. Numerous ctDNA biomarkers have been investigated based on their alterations such as 1) single nucleotide variations (either insertion or deletion of a nucleotide) markers including TP53, KRAS, and CCND1; 2) copy number variations which include markers such as CDK6, EFGR, MYC and BRAF; 3) DNA methylation (RASSF1A, SEPT9, KMT2C and CCNA2); 4) homozygous mutation includes ctDNA markers as CDKN2A, AXIN1; and 5) gain or loss of function of the genes, particularly for HCC. Various researchers have conducted many studies and gotten fruitful results. Still, there are some drawbacks to ctDNA namely low quantity, fragment heterogeneity, less stability, limited mutant copies and standards, and differential sensitivity. However, plenty of investigations demonstrate ctDNA's significance as a polyvalent biomarker for cancer and can be viewed as a future diagnostic, prognostic and therapeutic agent. This article overviews many conditions in genetic changes linked to the onset and development of HCC, such as dysregulated signaling pathways, somatic mutations, single-nucleotide polymorphisms, and genomic instability. Additionally, efforts are also made to develop treatments for HCC that are molecularly targeted and to unravel some of the genetic pathways that facilitate its early identification.
肝细胞癌(HCC)被认为是所有类型癌症中第五大常见癌症,发病率位列第三。它具有最频繁的复制时间和高复发率。最近,使用的最独特技术是液体活检,其携带多种标志物;最突出的是循环肿瘤DNA(ctDNA)。人们采用多种方法来研究ctDNA,包括各种形式的聚合酶链反应(PCR)[乳液PCR(ePCR)、数字PCR(dPCR)以及磁珠、乳液、扩增、磁性(BEAMing)PCR]。因此,ctDNA正被视为一种潜在的生物标志物,它能够实现癌症的早期检测、治疗监测,并且肿瘤负荷的预测数据对于治疗或手术具有主观性。基于其改变,众多ctDNA生物标志物已被研究,例如:1)单核苷酸变异(核苷酸的插入或缺失)标志物,包括TP53、KRAS和CCND1;2)拷贝数变异,包括CDK6、EFGR、MYC和BRAF等标志物;3)DNA甲基化(RASSF1A、SEPT9、KMT2C和CCNA2);4)纯合突变,包括CDKN2A、AXIN1等ctDNA标志物;5)基因的功能获得或丧失,特别是对于HCC。众多研究人员进行了许多研究并取得了丰硕成果。然而,ctDNA仍存在一些缺点,即数量少、片段异质性、稳定性较差、突变拷贝和标准有限以及灵敏度差异。尽管如此,大量研究表明ctDNA作为一种多价癌症生物标志物具有重要意义,并且可被视为未来的诊断、预后和治疗手段。本文概述了与HCC发生和发展相关的许多遗传变化情况,如信号通路失调、体细胞突变、单核苷酸多态性和基因组不稳定性。此外,还努力开发针对HCC的分子靶向治疗方法,并揭示一些有助于早期识别的遗传途径。