ANXA2P2 and PA2G4P4 Pseudogenes Are Associated with the Response to Ionizing Radiation and Could Be Used as Potential

Tomasz Kolenda1,2, Piotr Białas3, Kacper Kamiński4,5

  • 1Research and Implementation Unit, Greater Poland Cancer Center, Garbary Street 15, 61-866 Poznan, Poland.

Biomedicines
|January 28, 2026
PubMed

Insights

Two pseudogenes, ANXA2P2 and PA2G4P4, are upregulated in head and neck squamous cell carcinoma (HNSCC). Their expression correlates with aggressive tumors and poor radiotherapy response, suggesting potential as HNSCC biomarkers.

Area of Science:

  • Oncology
  • Genomics
  • Biomarker Discovery

Background:

  • Head and neck squamous cell carcinoma (HNSCC) is an aggressive cancer with limited prognostic and predictive biomarkers.
  • The clinical significance of pseudogenes, like ANXA2P2 and PA2G4P4, in HNSCC remains largely undefined.
  • Identifying novel biomarkers is crucial for improving HNSCC patient outcomes.

Purpose of the Study:

  • To investigate the expression and clinical relevance of pseudogenes ANXA2P2 and PA2G4P4 in HNSCC.
  • To assess the association of these pseudogenes with clinicopathological features, survival, and treatment response.
  • To explore their potential as prognostic and predictive biomarkers in HNSCC.

Main Methods:

  • Analysis of transcriptomic and clinical data from The Cancer Genome Atlas (TCGA) for HNSCC.
  • Bioinformatic assessment of ANXA2P2 and PA2G4P4 expression in relation to clinicopathological variables, HPV status, molecular subtypes, survival, genomic instability, radiotherapy response, and immune landscape.
  • Statistical analysis to determine correlations and significance.

Main Results:

  • Both ANXA2P2 and PA2G4P4 were significantly upregulated in HNSCC tissues compared to normal tissues.
  • Higher pseudogene expression correlated with adverse clinicopathological features, increased tumor proliferation, unfavorable molecular subtypes, and reduced overall survival.
  • Lower expression of ANXA2P2 and PA2G4P4 was associated with better radiotherapy response, improved survival outcomes, and distinct immune profiles.

Conclusions:

  • ANXA2P2 and PA2G4P4 are clinically relevant pseudogenes in HNSCC, linked to tumor aggressiveness and immune modulation.
  • These pseudogenes demonstrate potential as prognostic and predictive biomarkers for HNSCC patients, particularly concerning radiotherapy response.
  • Further functional studies are warranted to validate their role and therapeutic implications in HNSCC.

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