Mahdei Nasirmahalleh Nima, Hemmati Mina, Parsamanesh Negin
Student Research Committee, Department of Medical Biochemistry, School of Medicine, Zanjan, Iran.
Department of Clinical Biochemistry, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Iran J Pathol. 2025 Spring;20(2):181-197. doi: 10.30699/ijp.2025.2030953.3311. Epub 2025 Mar 10.
BACKGROUND & OBJECTIVE: Breast cancer (BC) is the most common type of malignant neoplasm and is the primary cause of mortality among women aged 45 to 55 years. Studies indicate that cancer displays irregular metabolic patterns in contrast to normal tissue. Furthermore, there is compelling evidence supporting the significant role of peroxisomes in the intricate metabolic processes of cancer. Peroxisomal biogenesis factors (PEXs), which are peroxisomal proteins, control activities such as the degradation and biogenesis of peroxisomes. Hence, the correlation between peroxisomal biogenesis factor expression and BC was explored, to introduce key proteins and potential biomarkers by analyzing.
This study utilized UALCAN, GenExMiner v4.8, Metascape, STRING, TIMER, the Kaplan-Meier plotter, The Human Protein Atlas, MirTarBase, and cBioportal.
The transcriptional levels of PEX6/7/10/11B/13/16 in BC tissues were significantly elevated, whereas the transcriptional levels of PEX2/3/5/11A/12/19 were significantly reduced. High expression levels of PEX 2/3/10/12/11G /26/13/16/14 were significantly related to shorter relapse-free survival, and higher mRNA expression of PEX 11B/11G/11A/12/19 was significantly associated with longer overall survival of BC patients. We identified has-miR-4318 and has-7106-3p as more correlated miRNAs with the PEX family.
Our results may provide novel insights for the selection of therapeutic targets and prognostic biomarkers for BC.
乳腺癌(BC)是最常见的恶性肿瘤类型,是45至55岁女性死亡的主要原因。研究表明,与正常组织相比,癌症表现出不规则的代谢模式。此外,有确凿证据支持过氧化物酶体在癌症复杂代谢过程中的重要作用。过氧化物酶体生物发生因子(PEXs)是过氧化物酶体蛋白,控制过氧化物酶体的降解和生物发生等活动。因此,本研究探讨了过氧化物酶体生物发生因子表达与BC之间的相关性,通过分析引入关键蛋白和潜在生物标志物。
本研究利用了UALCAN、GenExMiner v4.8、Metascape、STRING、TIMER、Kaplan-Meier绘图仪、人类蛋白质图谱、MirTarBase和cBioportal。
BC组织中PEX6/7/10/11B/13/16的转录水平显著升高,而PEX2/3/5/11A/12/19的转录水平显著降低。PEX 2/3/10/12/11G /26/13/16/14的高表达水平与无复发生存期缩短显著相关,PEX 11B/11G/11A/12/19的较高mRNA表达与BC患者较长的总生存期显著相关。我们确定了has-miR-4318和has-7106-3p是与PEX家族相关性更高的miRNA。
我们的结果可能为BC治疗靶点的选择和预后生物标志物提供新的见解。