Priya Shivani, Kma Lakhon
Department of Chemistry & Biochemistry, Sharda School of Basic Sciences & Research, Sharda University, Noida, UP, India.
Department of Biochemistry, North Eastern Hill University, Shillong, India.
Biochem Biophys Rep. 2025 Jan 10;41:101896. doi: 10.1016/j.bbrep.2024.101896. eCollection 2025 Mar.
Hepatocellular carcinoma (HCC) is the most fatal cancer that has affected both male and female populations globally. With poor diagnosis and patient survival rates, it has become a global need for scientists to come to the aid. The main objective of the study was to profile the miRNAs in the serum of Control and DEN-treated mice at different time intervals (4 Weeks, 8 Weeks, 12 Weeks, and 16 Weeks) and identify HCC-associated miRNA as putative early biomarkers along with the miRNA regulated candidate gene which may be involved in HCC. Our study group involves 4,8,12, & 16 weeks 16-week-old treated male mice. Each group was sacrificed and analyzed for the stages of HCC. We employed techniques for the small RNA-Seq and bioinformatics pipeline for further analysis. Our analysis revealed over 400 differentially expressed miRNAs in each treated sample and 10 novel miRNAs. The downstream analysis of these differentially expressed miRNAs, and their target genes opened an arena of different biological processes and pathways that these miRNAs affect during the development of HCC. The work has a promising role as the miRNAs predicted through this study can be used as biomarkers for early detection of HCC.
肝细胞癌(HCC)是全球影响男性和女性人群的最致命癌症。由于诊断和患者生存率较低,科学家们迫切需要提供帮助。该研究的主要目的是分析对照小鼠和经二乙基亚硝胺(DEN)处理的小鼠在不同时间间隔(4周、8周、12周和16周)血清中的微小RNA(miRNA),并将与HCC相关的miRNA鉴定为假定的早期生物标志物,同时鉴定可能参与HCC的miRNA调控候选基因。我们的研究组包括4周、8周、12周和16周龄经处理的雄性小鼠。每组小鼠处死后进行HCC阶段分析。我们采用了小RNA测序技术和生物信息学流程进行进一步分析。我们的分析在每个处理样本中发现了400多个差异表达的miRNA和10个新的miRNA。对这些差异表达的miRNA及其靶基因的下游分析揭示了这些miRNA在HCC发生过程中影响的不同生物学过程和途径。这项工作具有重要意义,因为通过本研究预测的miRNA可作为HCC早期检测的生物标志物。