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Prognostic Value of HHLA2 in Patients with Solid Tumors: A Meta-Analysis
Agnieszka Kula1, Miriam Dawidowicz1, Sylwia Mielcarska2
1Department of Oncological Surgery, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 41-808 Katowice, Poland.
International Journal of Molecular Sciences
|May 11, 2024
Summary
High HHLA2 expression in solid tumors correlates with worse patient outcomes. This meta-analysis found elevated HHLA2 levels are linked to shorter survival and increased recurrence rates in cancer patients.
Area of Science:
- Immunology
- Oncology
- Biomarker Research
Background:
- HHLA2 is a B7 family checkpoint molecule with dual co-stimulatory/co-inhibitory functions in cancer immunity.
- Its precise impact on solid cancer patient prognosis remains incompletely understood.
Purpose of the Study:
- To conduct a meta-analysis evaluating the association between HHLA2 expression levels and prognosis in patients with solid cancers.
- To synthesize evidence from multiple studies to determine the clinical significance of HHLA2 in solid tumors.
Main Methods:
- Systematic literature search of PubMed, Embase, Web of Science, Cochrane, and SCOPUS databases.
- Meta-analysis of 18 studies including 2880 patients, assessing overall survival (OS), recurrence-free survival (RFS), and disease-free survival (DFS).
- Hazard ratios (HR) were pooled using R studio software to quantify survival outcomes.
Main Results:
- High HHLA2 expression was significantly associated with worse OS (HR = 1.58).
- Elevated HHLA2 levels correlated with shorter RFS (HR = 1.95) and worse DFS (HR = 1.45).
- These findings were consistent across multiple solid cancer types.
Conclusions:
- High HHLA2 expression serves as a negative prognostic biomarker in solid cancers.
- Targeting HHLA2 may represent a potential therapeutic strategy to improve patient outcomes.
- Further research is warranted to elucidate the mechanisms underlying HHLA2's role in cancer progression.
Keywords:
HHLA2disease-free survival (DFS)meta-analysisoverall survival (OS)progression-free survival (PFS)recurrence-free survival (RFS)solid cancers
