Department of Dermatology, Firat University Hospital, Elazig, Turkey.
Department of Dermatology. TR23119, Firat University Faculty of Medicine, Elazig, Turkey.
Arch Dermatol Res. 2024 Oct 14;316(10):675. doi: 10.1007/s00403-024-03417-y.
In this study, we aimed to investigate the potential contributions to the disease by examining the immunoreactivities of SPX in LP-affected skin tissue using immunohistochemical methods, in light of its recent prominence as a molecule related to diabetes mellitus, along with apoptosis and ferroptosis mediated by GPX4 and TRPM2 channels facilitating oxidative stress-induced cell death.
This research explored the immunohistochemical expressions of TRPM2, GPX4, and SPX in Lichen Planus (LP) patients compared to healthy individuals.
Forty skin samples were collected, split equally between LP patients and healthy controls, excluding those with other conditions. Samples underwent immunohistochemical staining for TRPM2, SPX, and GPX4, using secondary antibodies and chromogens AEC or DAB. Histoscores were calculated based on staining diffusiveness and severity. Statistical analyses were performed with SPSS 22.0, using t-tests and ANOVA, with significance set at p < 0.05.
There were no demographic differences between groups (p > 0.05). LP patients showed significantly lower TRPM2 and GPX4 histoscores and higher SPX histoscores compared to controls (TRPM2 and GPX4: p < 0.001, SPX: p < 0.001). Gender and age did not affect histoscores significantly.
Findings suggest TRPM2, GPX4, and SPX play roles in LP pathogenesis, indicating a need for further molecular studies to clarify their involvement. This contributes to understanding LP beyond the traditional apoptosis perspective.
在这项研究中,我们旨在通过使用免疫组织化学方法检查 LP 影响皮肤组织中 SPX 的免疫反应性,来研究其作为与糖尿病相关的分子的潜在贡献,同时还研究了 GPX4 和 TRPM2 通道介导的细胞凋亡和铁死亡,以促进氧化应激诱导的细胞死亡。
本研究探讨了与健康个体相比,TRPM2、GPX4 和 SPX 在扁平苔藓(LP)患者中的免疫组织化学表达。
收集了 40 个皮肤样本,平均分为 LP 患者和健康对照组,排除了其他疾病的患者。对样本进行了 TRPM2、SPX 和 GPX4 的免疫组织化学染色,使用了二级抗体和 AEC 或 DAB 显色剂。根据染色扩散度和严重程度计算了组织评分。使用 SPSS 22.0 进行了统计分析,采用了 t 检验和 ANOVA,显著性水平设为 p<0.05。
两组之间在人口统计学方面没有差异(p>0.05)。与对照组相比,LP 患者的 TRPM2 和 GPX4 组织评分显著降低,而 SPX 组织评分显著升高(TRPM2 和 GPX4:p<0.001,SPX:p<0.001)。性别和年龄对组织评分没有显著影响。
研究结果表明,TRPM2、GPX4 和 SPX 在 LP 发病机制中发挥作用,表明需要进一步进行分子研究以阐明其参与的情况。这有助于超越传统的细胞凋亡视角来理解 LP。