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April 15, 2026Cancer Medicine0 citationsOpen Access

Immunohistochemical Analysis of Potential Therapeutic Targets PRAME , FOLR1 , and CLDN18.2 in Salivary Gland Carcinomas

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LBLukas BrustUniversitätsklinikum des SaarlandesJKJan Philipp KühnSaarland UniversitySKSandrina KörnerSaarland University

Key Points

  • The study aims to assess the expression of PRAME, FOLR1, and CLDN18.2 as potential therapeutic targets in salivary gland carcinomas.
  • Analyzed tumor samples from 54 patients with various subtypes of salivary gland carcinomas.
  • Utilized immunohistochemistry to evaluate biomarker expression.
  • Scored biomarker expression using the Immunoreactive Score.
  • PRAME was strongly expressed in 89% of cases, while FOLR1 and CLDN18.2 were expressed in 41% and 6%, respectively.
  • High PRAME expression was linked to distant metastases across histological subtypes.
  • Patients with low PRAME expression showed improved overall survival according to Kaplan-Meier analysis.

Abstract

Salivary gland carcinomas are rare, heterogeneous, and often resistant to conventional treatments, highlighting the need for new therapeutic strategies. This retrospective study evaluated the expression of three immunologically relevant biomarkers-PRAME, FOLR1, and CLDN18.2-as potential therapeutic targets in salivary gland carcinomas. Tumor samples from 54 patients with seven histological subtypes treated at Saarland University Medical Center between 2013 and 2023 were analyzed using immunohistochemistry and scored with the Immunoreactive Score. PRAME was strongly expressed in 89% of cases, while FOLR1 and CLDN18.2 showed markedly lower expression at 41% and 6%, respectively. High PRAME expression was significantly associated with the presence of distant metastases, regardless of histological subtype. Patients with low PRAME expression tended to have improved overall survival, as indicated by Kaplan-Meier analysis and Log-Rank testing. These findings suggest PRAME as a promising immunotherapeutic and diagnostic target for salivary gland carcinomas, particularly through T-cell-based therapies already under investigation in other malignancies such as acute myeloid leukemia. Further preclinical studies are needed to validate the functional and therapeutic significance of PRAME, FOLR1, and CLDN18.2 in this context.

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Cite This Study

Brust et al. (2026) studied this question.

synapsesocial.com/papers/69df2abce4eeef8a2a6afc5ehttps://doi.org/10.1002/cam4.71799
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