# Pan-cancer analysis of integrin alpha family and prognosis validation in head and neck squamous cell carcinoma

**Authors:** Shaojie Ji, Fang Hao, Chenghui Zhang, Chunyan Hu, Henglei Ren, Qiang Huang, Jifeng Gu

PMC · DOI: 10.3389/fonc.2025.1556226 · Frontiers in Oncology · 2026-01-12

## TL;DR

This study explores how integrin alpha family genes are linked to cancer progression and poor outcomes, especially in head and neck squamous cell carcinoma.

## Contribution

The study identifies ITGA family genes as potential biomarkers and therapeutic targets through pan-cancer analysis and HNSC validation.

## Key findings

- ITGA family genes are abnormally expressed in most tumors and linked to poor prognosis.
- High expression of ITGA3/5/6 in HNSC is associated with poor patient outcomes.
- Genetic changes in ITGA genes, like amplifications, correlate with worse survival.

## Abstract

Integrins are cell-surface receptors involved in the interaction of cells with the extracellular matrix and are essential for processes such as cell adhesion, migration, and proliferation. However, the specific mechanisms by which integrin α family (ITGA) genes contribute to tumorigenesis and progression remain to be thoroughly explored.

In this study, based on The Cancer Genome Atlas, we explored the differential expression of ITGA family genes in 33 types of tumors and normal tissues. Univariate COX regression was employed to analyze its association with the survival outcomes of pan-cancer patients. Online tools were utilized to analyze genetic changes of the genes, study the relationship with immune subtypes and evaluate immune cells, and analyze the relationship with tumor mutational burden and stemness. Additionally, immunohistochemistry experiments were conducted on Head and neck squamous cell carcinoma (HNSC) tissue samples to assess the impact of ITGA3 and others on patient prognosis.

ITGA family genes are abnormally expressed in most tumors and are significantly associated with poor prognosis. Genetic changes in these genes are mainly amplifications, and the mutation group has a poor prognosis. The differential expression of ITGA family genes is related to increased immune-related scores and immune cells. In HNSC, the high expression of ITGA3/5/6 serves as a biomarker for poor prognosis.

Our research results indicate that ITGA family genes can serve as valuable prognostic biomarkers and therapeutic targets for tumors.

## Linked entities

- **Genes:** ITGA3 (integrin subunit alpha 3) [NCBI Gene 3675], ITGA5 (integrin subunit alpha 5) [NCBI Gene 3678], ITGA6 (integrin subunit alpha 6) [NCBI Gene 3655]
- **Diseases:** Head and neck squamous cell carcinoma (MONDO:0010150), cancer (MONDO:0004992)

## Full-text entities

- **Genes:** ITGA3 (integrin subunit alpha 3) [NCBI Gene 3675] {aka CD49C, FRP-2, GAP-B3, GAPB3, ILNEB, JEB7}
- **Diseases:** HNSC (MESH:D000077195), Cancer (MESH:D009369), tumorigenesis (MESH:D063646)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12833762/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833762/full.md

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Source: https://tomesphere.com/paper/PMC12833762