Dorofeeva Anna, Kobzeva Ksenia, Soldatov Vladislav, Bushueva Olga
Laboratory of Genomic Research, Research Institute for Genetic and Molecular Epidemiology, Kursk State Medical University, Kursk, Russia.
Laboratory of Brain Circuit Therapeutics, Achucarro Basque Center for Neuroscience, Leioa, Bizkaia, Spain.
Neuromolecular Med. 2025 Sep 4;27(1):62. doi: 10.1007/s12017-025-08885-7.
The recently discovered family of heat-resistant obscure (Hero) proteins represents a novel class with chaperone-like activity and unique protective properties. These proteins may contribute to cellular survival in ischemic stroke (IS) conditions. Herein, we aimed to investigate the expression dynamics of six Hero genes during the acute and subacute phases of IS. Peripheral blood samples were collected from IS patients in the acute (day 1, n = 47) and subacute (day 7, n = 41) phases, along with healthy controls (n = 42). Gene expression was assessed via quantitative PCR. Statistical analysis included group comparisons, multivariate regression modelling, and correlation analysis. In the acute phase, C9orf16 (P = 0.006), C11orf58 (P = 0.00001), and SERBP1 (P = 0.006) were significantly downregulated compared to controls. By day 7, SERBP1 expression normalized, while C9orf16 (P = 0.002) and C11orf58 (P = 0.0004) remained downregulated. Multivariate regression identified C11orf58 expression as a potential biomarker of IS. Expression levels of SERBP1 and C11orf58 negatively correlated with infarct size during both the acute (R = - 0.59, P = 0.00012; R = - 0.49, P = 0.004) and subacute phases (R = - 0.54, P = 0.0024; R = - 0.44, P = 0.032). eQTL analysis showed that SERBP1 SNPs were associated with reduced expression only in controls. Our findings underscore the potential relevance of Hero proteins as biomarkers or therapeutic targets in IS, warranting further investigation into their mechanistic involvement in neuroprotection and recovery.
最近发现的耐热性未知(Hero)蛋白家族代表了一类具有伴侣样活性和独特保护特性的新型蛋白。这些蛋白可能有助于细胞在缺血性中风(IS)条件下存活。在此,我们旨在研究六种Hero基因在IS急性期和亚急性期的表达动态。收集了IS急性期(第1天,n = 47)和亚急性期(第7天,n = 41)患者的外周血样本,以及健康对照(n = 42)。通过定量PCR评估基因表达。统计分析包括组间比较、多变量回归建模和相关性分析。在急性期,与对照组相比,C9orf16(P = 0.006)、C11orf58(P = 0.00001)和SERBP1(P = 0.006)显著下调。到第7天,SERBP1表达恢复正常,而C9orf16(P = 0.002)和C11orf58(P = 0.0004)仍下调。多变量回归确定C11orf58表达为IS的潜在生物标志物。在急性期(R = - 0.59,P = 0.00012;R = - 0.49,P = 0.004)和亚急性期(R = - 0.54,P = 0.0024;R = - 0.44,P = 0.032),SERBP1和C11orf58的表达水平与梗死面积均呈负相关。eQTL分析表明,SERBP1单核苷酸多态性仅在对照组中与表达降低相关。我们的研究结果强调了Hero蛋白作为IS生物标志物或治疗靶点的潜在相关性,有必要进一步研究它们在神经保护和恢复中的机制作用。