Lee Haneul, Lee Eun Ju, Park Kwangmin, Lee Dong Geon, Kim Ah Yeoung, Park Sunyoung, Kim Jungho
Department of Forensic Science, Graduate school, Catholic University of Pusan, Busan 46252, Republic of Korea; Next-Generation Industrial Field-Based Specialist Program for Molecular Diagnostics, Brain Busan 21 Plus Project, Graduate School, Catholic University of Pusan, Republic of Korea.
Department of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Republic of Korea; Next-Generation Industrial Field-Based Specialist Program for Molecular Diagnostics, Brain Busan 21 Plus Project, Graduate School, Catholic University of Pusan, Republic of Korea; Korea Mycobacterium Resource Center (KMRC), Department of Research and Development, The Korean Institute of Tuberculosis, Osong, 28158, Republic of Korea.
Forensic Sci Int. 2025 May;370:112473. doi: 10.1016/j.forsciint.2025.112473. Epub 2025 Apr 12.
Estimating the post-mortem interval (PMI) is a critical aspect of forensic science; however, current methods often lack precision because of the variability in external and internal factors. This study investigated the potential use of microRNAs (miRNAs) as stable molecular biomarkers for PMI estimation. We analysed the miRNA expression profiles in myocardial tissue from 18 BALB/c mice sampled at six PMIs (0, 12, 24, 36, 48 h, and 6 d) using high-throughput sequencing and qRT-PCR. In total, 154 differentially expressed (DE) miRNAs were identified, of which 55 were upregulated and 99 were downregulated. Five upregulated (miR-206-3p, miR-200a-3p, miR-205-5p, miR-200b-3p, miR-429-3p) and four downregulated (miR-541-5p, miR-455-3p, miR-30c-5p, and miR-149-5p) apoptosis-related miRNAs were validated through qRT-PCR analysis, indicating their potential as supportive biomarkers in PMI estimation. Gene ontology analysis revealed their involvement in processes such as cardiac muscle cell proliferation, nuclear migration, and miRNA metabolic regulation. Linear regression models demonstrated significant correlations between specific miRNA expression levels and the PMI. These findings provide a molecular basis that may contribute to improving PMI estimation accuracy and supporting forensic methodologies.
估计死后间隔时间(PMI)是法医学的一个关键方面;然而,由于外部和内部因素的变异性,目前的方法往往缺乏精确性。本研究调查了微小RNA(miRNA)作为稳定分子生物标志物用于PMI估计的潜在用途。我们使用高通量测序和qRT-PCR分析了在六个PMI(0、12、24、36、48小时和6天)采集的18只BALB/c小鼠心肌组织中的miRNA表达谱。总共鉴定出154个差异表达(DE)的miRNA,其中55个上调,99个下调。通过qRT-PCR分析验证了五个上调的(miR-206-3p、miR-200a-3p、miR-205-5p、miR-200b-3p、miR-429-3p)和四个下调的(miR-541-5p、miR-455-3p、miR-30c-5p和miR-149-5p)凋亡相关miRNA,表明它们作为PMI估计中辅助生物标志物的潜力。基因本体分析揭示了它们参与心肌细胞增殖、核迁移和miRNA代谢调控等过程。线性回归模型显示特定miRNA表达水平与PMI之间存在显著相关性。这些发现提供了一个分子基础,可能有助于提高PMI估计的准确性并支持法医方法。