# InfoScan: A New Transcript Identification Tool Based on scRNA-Seq and Its Application in Glioblastoma

**Authors:** Shiqiang Mei, Jinjin Huang, Zhen Zhang, Haotian Lei, Qiaojuan Huang, Lianghu Qu, Lingling Zheng

PMC · DOI: 10.3390/ijms26052208 · International Journal of Molecular Sciences · 2025-02-28

## TL;DR

InfoScan is a new tool for analyzing scRNA-seq data that helps identify rare cell types in glioblastoma and reveals potential treatment targets.

## Contribution

InfoScan introduces a novel method for identifying unannotated transcripts and rare cell populations in scRNA-seq data.

## Key findings

- A rare 'neoplastic-stemness' subpopulation with cancer stem cell-like features was identified in glioblastoma.
- TAMs secrete SPP1, which activates the PI3K/AKT pathway in neoplastic-stemness cells to promote metastasis.
- Neoplastic-stemness cells may be sensitive to omipalisib, a PI3K inhibitor, suggesting a potential therapeutic strategy.

## Abstract

InfoScan is a novel bioinformatics tool designed for the comprehensive analysis of full-length single-cell RNA sequencing (scRNA-seq) data. It enables the identification of unannotated transcripts and rare cell populations, providing a powerful platform for transcriptome characterization. In this study, InfoScan was applied to glioblastoma multiforme (GBM), identifying a rare “neoplastic-stemness” subpopulation exhibiting cancer stem cell-like features. Functional analyses suggested that tumor-associated macrophages (TAMs) secrete SPP1, which binds to CD44 on neoplastic-stemness cells, activating the PI3K/AKT pathway and driving lncRNA transcription to promote metastasis. Integration of TCGA and CGGA datasets further supported these findings, highlighting key mutations associated with the neoplastic-stemness subpopulation. Drug sensitivity assays indicated that neoplastic-stemness cells might be sensitive to omipalisib, a PI3K inhibitor, pointing to a potential therapeutic target. InfoScan offers a robust framework for exploring complex transcriptomic landscapes and characterizing rare cell populations, providing valuable insights into GBM biology and advancing precision cancer therapy.

## Linked entities

- **Genes:** CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207]
- **Proteins:** SPP1 (secreted phosphoprotein 1)
- **Chemicals:** omipalisib (PubChem CID 25167777)
- **Diseases:** glioblastoma multiforme (MONDO:0018177), glioblastoma (MONDO:0018177)

## Full-text entities

- **Genes:** SPP1 (secreted phosphoprotein 1) [NCBI Gene 6696] {aka BNSP, BSPI, ETA-1, OPN}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}
- **Diseases:** cancer (MESH:D009369), metastasis (MESH:D009362), GBM (MESH:D005909)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11900204/full.md

## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC11900204/full.md

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Source: https://tomesphere.com/paper/PMC11900204