Programmed cell death ligand 1 in correlation with BRAFV600E mutation, molecular characteristics and biological behavior in ameloblastoma - Report - MDSpire

Programmed cell death ligand 1 in correlation with BRAFV600E mutation, molecular characteristics and biological behavior in ameloblastoma

  • By

  • Aijing Pan

  • Zhipeng Xie

  • Jianhui Zhan

  • Yifeng Zhao

  • Yue Du

  • Kai Zhang

  • June 16, 2026

  • 0 min

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Clinical Report: Association of PD-L1 with BRAFV600E Mutation in Ameloblastoma

Overview

Revise to specify the clinical relevance of CD8+ T cell infiltration in relation to PD-L1 expression.

Background

Ameloblastoma is a prevalent odontogenic tumor with a high recurrence rate and potential for malignant transformation. The BRAFV600E mutation is commonly found in AM, suggesting a role in tumor pathogenesis and potential targeted therapies. Understanding the immune microenvironment, particularly PD-L1 expression, may inform treatment strategies and improve patient outcomes.

Data Highlights

ParameterFindings
PD-L1 Positive Cases42/50 (84%)
BRAF Mutation Positive41/50 (82%)
PD-L1 Positivity in BRAF Positive38/41 (92.68%)
Correlation p-value0.003
CD8+ T Cell Infiltration and DFSHR = 0.112, p = 0.041

Key Findings

  • 84% of AM patients showed PD-L1 positivity.
  • 92.68% of BRAF mutation-positive cases were PD-L1 positive (p = 0.003).
  • No significant correlation between PD-L1 and CD8+ T cells or FoxP3+ cells.
  • High CD8+ T cell infiltration is associated with improved disease-free survival (HR = 0.112, p = 0.041).
  • PD-L1 expression does not correlate with major clinicopathological parameters of AM.

Clinical Implications

The high prevalence of PD-L1 expression in BRAFV600E-mutated AM suggests that PD-L1 may serve as a potential therapeutic target. Additionally, assessing CD8+ T cell infiltration could provide prognostic information regarding disease-free survival, guiding treatment decisions.

Conclusion

The findings highlight the significant association between PD-L1 expression and the BRAFV600E mutation in ameloblastoma, with implications for targeted therapy and immunotherapy. Further studies are warranted to validate these results in larger cohorts.

Related Resources & Content

  1. Blood Cancer Journal, 2015 -- BRAF V600E mutation in early-stage multiple myeloma: good response to broad acting drugs and no relation to prognosis
  2. Blood Cancer Journal, 2013 -- Lack of BRAF V600E mutation in human myeloma cell lines established from myeloma patients with extramedullary disease
  3. Acta Neuropathologica, 2014 -- BRAF V600E Mutations Are Distinctive in Papillary Craniopharyngioma and May Occur Alongside CTNNB1 Mutations in Adamantinomatous Craniopharyngioma
  4. Blood Cancer Journal, 2022 -- Implications for Treatment and Diagnosis of BRAF Fusions in Histiocytic Disorders
  5. Precision therapy for BRAF V600E–mutated ameloblastoma: Systematic review insights - ScienceDirect
  6. Molecular-targeted therapy in ameloblastoma: a systematic review - PMC
  7. Programmed death-ligand 1 regulates ameloblastoma growth and recurrence
  8. Contemporary management of ameloblastoma
  9. Molecular-targeted therapy in ameloblastoma
  10. Programmed death-ligand 1 regulates ameloblastoma growth and recurrence

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