ORIGINAL RESEARCH article

Front. Cell Dev. Biol.

Sec. Cancer Cell Biology

AC005034.3/hsa-miR-126-5p/EIF3H Axis: Bioinformatics Analysis, Expression Validation, and Association with Prognosis and Immunosuppressive Microenvironment in Pancreatic Adenocarcinoma

  • 1. Ganzhou Cancer Hospital, Ganzhou 341000, Jiangxi Province, China., Ganzhou, China

  • 2. Zhangye People's Hospital Affiliated to Hexi University, Zhangye, China

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Abstract

Background: Pancreatic adenocarcinoma (PAAD) ranks among the most lethal human solid tumors, distinguished by its swift progression and limited effective treatment options. The eukaryotic translation initiation factor 3 subunit H (EIF3H) is postulated to be a critical factor in translational initiation, with emerging research indicating its potential involvement in promoting tumor invasion and metastasis. Nevertheless, the precise role of EIF3H within tumors remains insufficiently understood. Methods and Results: Employing a comprehensive pan-cancer methodology, we conducted an analysis of datasets from The Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), ArrayExpress, and the International Cancer Genome Consortium (ICGC). This analysis systematically assessed the prognostic significance, clinical associations, signaling pathways, immune infiltration profiles, and chemotherapeutic sensitivity associated with EIF3H expression. Through a series of correlation, expression, and survival analyses, we identified noncoding RNAs (ncRNAs) that contribute to the upregulation of EIF3H in pancreatic adenocarcinoma (PAAD). Notably, we identified the AC005034.3/hsa-miR-126-5p axis as the most promising upstream ncRNA-related pathway influencing EIF3H expression in PAAD. The differential expression of these three genes between PAAD and normal pancreatic tissues was further validated using reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and immunohistochemistry (IHC). Additionally, we demonstrated significant correlations between EIF3H expression and immune infiltration profiles, as well as chemotherapeutic sensitivity in PAAD. Furthermore, we constructed a protein-protein interaction (PPI) network and performed functional annotations involving EIF3H. Conclusion: our findings indicate that ncRNA-driven overexpression of EIF3H is associated with poor prognosis and tumor immune cell infiltration in PAAD, suggesting that the AC005034.3/hsa-miR-126-5p/EIF3H axis may serve as a promising prognostic biomarker and therapeutic target in PAAD

Summary

Keywords

EIF3H, Immune infiltration, ncRNAs, Pancreatic adenocarcinoma, prognosis

Received

14 October 2025

Accepted

31 January 2026

Copyright

© 2026 Sun, Song, Zhang, Wang, Wen, Wang and Qiu. 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: Kai Sun

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