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Perspectives from machine learning and multi-omics to decoding the effects of VDAC2 malignant subsets on tumor evolution
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  • Published: 31 March 2026

Perspectives from machine learning and multi-omics to decoding the effects of VDAC2 malignant subsets on tumor evolution

  • Jianing Yan1 na1,
  • Jingzhi Wang2 na1,
  • Haotian Dong1,
  • Guoliang Ye1 &
  • …
  • Yongfu Shao1 

npj Precision Oncology , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomarkers
  • Cancer
  • Computational biology and bioinformatics
  • Oncology

Abstract

VDAC2’s known role in cancer and immune regulation via enhancing the CD8+ T cell-mediated killing, and it is worth systematically digging out the role of VDAC2 in pan-cancer based on this research. Bulk RNA sequencing, single-cell RNA sequencing, and spatial transcriptomic analyses were utilized to explore the role of VDAC2 from multiple perspectives in pan-cancers. RT-PCR, cell co-culture, CCK-8 assay, Transwell invasion assays, and ELISA were performed to validate the expression level and biological function. VDAC2 was upregulated in the majority of pan-cancers, and functional enrichment analyses displayed that VDAC2 may take part in the biological progress of energy metabolism, mitochondrial damage and cell proliferation. The landscape of VDAC2 expression and immune infiltration was constructed, and the VDAC2-BAK1-IFNγ pathway was identified in digestive cancer. VDAC2 had the potential to serve as a novel prognostic, screening cancer indicator and immune therapeutic target sensitive to various drugs. Overexpression of VDAC2 significantly promoted gastric cancer cell proliferation, invasion and immune invasion, as validated in vitro experiments. In short, our pan-cancer analysis constructed a comprehensive landscape of VDAC2’s oncogenic role, establishing VDAC2 + -BAK1-IFNγ as an important pathway in tumor progression and immune evasion. VDAC2 emerges not only as a valuable prognostic biomarker but also as a promising novel therapeutic target.

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Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Acknowledgements

We thank the Home for Researchers editorial team (www.home-for-researchers.com) that helps as for the language editing service and Figdraw for drawing pictures. We thank Sparkle (https://grswsci.top/analyze/) for multi-omics data analysis. This study was funded by the Ningbo Top Medical and Health Research Program (No. 2023020612) and the Key Scientific and Technological Projects of Ningbo (No. 2021Z133).

Author information

Author notes
  1. These authors contributed equally: Jianing Yan, Jingzhi Wang.

Authors and Affiliations

  1. Department of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, China

    Jianing Yan, Haotian Dong, Guoliang Ye & Yongfu Shao

  2. Department of Radiotherapy Oncology, The First People’s Hospital of Yancheng, Yancheng, Jiangsu, China

    Jingzhi Wang

Authors
  1. Jianing Yan
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  2. Jingzhi Wang
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  3. Haotian Dong
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  5. Yongfu Shao
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Contributions

Yan and Shao made outstanding contributions to identify this manuscript. Ye revised it critically for vital intellectual content. Dong and Wang completed PCR and functional experiment in vitro. Yan drew the figure and wrote the draft. All authors contributed to the figures and approved the final submitted manuscript.

Corresponding authors

Correspondence to Guoliang Ye or Yongfu Shao.

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The authors declare no competing interests.

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Cite this article

Yan, J., Wang, J., Dong, H. et al. Perspectives from machine learning and multi-omics to decoding the effects of VDAC2 malignant subsets on tumor evolution. npj Precis. Onc. (2026). https://doi.org/10.1038/s41698-026-01394-1

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  • Received: 24 September 2025

  • Accepted: 16 March 2026

  • Published: 31 March 2026

  • DOI: https://doi.org/10.1038/s41698-026-01394-1

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