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MTHFD1L是皮肤黑色素瘤中一种新的预后标志物和治疗靶点。

MTHFD1L is a novel prognostic marker and therapeutic target in cutaneous melanoma.

作者信息

Xie Xinlian, Shi Guangfu, Ning Kebin, Wu Zhenjie

机构信息

Department of Bone and Soft Tissue Surgery, Guangxi Medical University Cancer Hospital, Hedi Rd. #71, Nanning, 530021, Guangxi, China.

出版信息

Diagn Pathol. 2025 Jul 10;20(1):83. doi: 10.1186/s13000-025-01680-9.

Abstract

BACKGROUND

Skin cutaneous melanoma (SKCM) is one of the highly malignant tumor. This study aimed to investigate the expression levels of MTHFD1L in cutaneous melanoma and to uncover its potential biological significance.

METHODS

This investigation employed the TCGA-SKCM dataset along with combined GSE15605 and GSE19234 datasets to analyze MTHFD1L expression patterns. Comprehensive bioinformatics analyses were conducted, including GO and KEGG pathway enrichment analyses, protein-protein interaction network construction, and evaluation of the relationship between MTHFD1L expression and immune infiltration. Prognostic significance was assessed using the GEPIA2 database. Experimental validation involved: (1) RT-qPCR, Western blot, and IHC staining to compare MTHFD1L expression between SKCM and normal tissues; (2) establishment of MTHFD1L knockdown models in A375 and 2058 cell lines for functional characterization.

RESULTS

The MTHFD1L level was increasing in SKCM tissues from GSE15605/GSE19234 and TCGA-SKCM, and high MTHFD1L expression correlated with poor overall survival. The RT-qPCR, Western blot and IHC confirmed the accuracy of bioinformatics. Knockdown of MTHFD1L significantly inhibited proliferation, migration, invasion, and clonogenic ability in A375 and A2058 melanoma cells, potentially through regulation of the TGF-β/SMAD signaling pathway.

CONCLUSION

MTHFD1L is a potential biomarker in cutaneous melanoma, and could potentially serve as a therapeutic target for SKCM.

摘要

背景

皮肤黑色素瘤(SKCM)是一种高度恶性的肿瘤。本研究旨在探讨MTHFD1L在皮肤黑色素瘤中的表达水平,并揭示其潜在的生物学意义。

方法

本研究使用TCGA-SKCM数据集以及合并的GSE15605和GSE19234数据集来分析MTHFD1L的表达模式。进行了全面的生物信息学分析,包括GO和KEGG通路富集分析、蛋白质-蛋白质相互作用网络构建以及评估MTHFD1L表达与免疫浸润之间的关系。使用GEPIA2数据库评估预后意义。实验验证包括:(1)RT-qPCR、蛋白质免疫印迹和免疫组化染色,以比较SKCM组织和正常组织中MTHFD1L的表达;(2)在A375和2058细胞系中建立MTHFD1L敲低模型以进行功能表征。

结果

来自GSE15605/GSE19234和TCGA-SKCM的SKCM组织中MTHFD1L水平升高,且MTHFD1L高表达与总体生存率差相关。RT-qPCR、蛋白质免疫印迹和免疫组化证实了生物信息学的准确性。敲低MTHFD1L可显著抑制A375和A2058黑色素瘤细胞的增殖、迁移、侵袭和克隆形成能力,可能是通过调节TGF-β/SMAD信号通路实现的。

结论

MTHFD1L是皮肤黑色素瘤的潜在生物标志物,并可能作为SKCM的治疗靶点。

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