Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Oncol.

Sec. Neuro-Oncology and Neurosurgical Oncology

ASPHD1 Is a Tumor-Suppressive and Prognostic Marker in Glioma

Provisionally accepted
Jinhua  YangJinhua YangFenfei  GaoFenfei Gao*Xiaowan  WangXiaowan WangYanmei  ZhangYanmei Zhang
  • Shantou University Medical College, Shantou, China

The final, formatted version of the article will be published soon.

Glioma is a highly aggressive primary brain tumor. To identify novel prognostic biomolecules and potential therapeutic targets, we investigated Aspartate beta-hydroxylase domain-containing protein 1 (ASPHD1), encoded by the ASPHD1 gene and predicted to function as a Fe (II)/2-oxoglutarate–dependent dioxygenase involved in peptide amino-acid modification. ASPHD1 has not previously been characterized in glioma. We assessed its expression and prognostic value using transcriptomic data from the Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), and Chinese Glioma Genome Atlas (CGGA). Co-expressed gene enrichment and DNA-methylation analyses were performed, and associations between ASPHD1 expression and overall survival (OS) were evaluated. Gene Ontology and KEGG analyses of ASPHD1 co-expressed genes indicated enrichment in synaptic signaling, ion-channel activity, and calcium-signaling pathways, suggesting a link with neuronal and synaptic function. ASPHD1 expression showed a pronounced inverse correlation with WHO grade, and higher ASPHD1 expression was associated with prolonged OS; multivariable Cox models identified low ASPHD1 as an independent adverse prognostic factor. Pan-cancer analysis further revealed that higher ASPHD1 expression was associated with longer OS in skin cutaneous melanoma (SKCM), uveal melanoma (UVM), and mesothelioma (MESO). In glioma cell lines, ASPHD1 overexpression suppressed proliferation, migration, and invasion in vitro, and inhibited tumor growth in a subcutaneous U87 xenograft model. ASPHD1 overexpression also upregulated neuronal differentiation–related genes, produced more negative resting membrane potentials on whole-cell patch-clamp recordings, enhanced depolarization-evoked Ca²⁺ transients on calcium imaging, and increased NeuN protein expression. Together, these findings identify ASPHD1 as a favorable prognostic biomarker in glioma and suggest that high ASPHD1 expression restrains glioma progression while promoting neuron-like differentiation of glioma cells.

Keywords: ASPHD1, Glioma, proliferation, neuronal differentiation, Calcium Signaling, Diagnostic biomarker, prognostic biomarker

Received: 28 Aug 2025; Accepted: 08 Dec 2025.

Copyright: © 2025 Yang, Gao, Wang and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Fenfei Gao

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.