An Insight into Prognostic Impact of TIPE2 & CD36 Immunohistochemical Expression in Urothelial Carcinoma

Document Type : Original Research

Authors

1 Pathology Department, Faculty of Medicine, Menoufia University, Shebin El Kom, Egypt

2 Department of pathology, Faculty of Medicine, Zagazig University, Egypt

Abstract
Background & Objective: Even though fast advances in the detection and management of bladder carcinoma, the number of deaths remains high. Therefore, the identification of an effective biomarker predicting tumor progression in cancer bladder patients is a crucial issue. This study aims to identify TIPE2 and CD36 expressions in cancer bladder and examine their relationship with clinicopathological data and prognosis.
Methods: Using immunohistochemistry, we investigated 60 specimens of bladder urothelial cancer (UC) for the expression of TIPE2 and CD36 and compared them with clinicopathologic parameters and survival data. Furthermore, we investigate the association between TIPE2 and CD36 expression and Vimentin expression to elucidate the influence of TIPE2 and CD36 on the epithelial-mesenchymal transition (EMT) in UC.
Results: TIPE2 expression was associated with lower stages and prolonged disease-free survival (DFS) and overall survival (OS). Therefore, TIPE2 may be considered a good indicator of UC prognosis. CD36 immuno-positivity was associated with high tumor grade, stages, shorter OS, and DFS. Therefore, the immune positivity of CD36 may be a poor prognostic marker for UC patients. Furthermore, Vimentin expression was directly correlated with CD36 expression and inversely correlated with TIPE2 expression.
Conclusion: TIPE2 and CD36 may be novel biomarkers for predicting tumor metastasis and prognosis in patients with bladder UC and hold promise as therapeutic targets.

Highlights

  • Positive TIPE2 immunohistochemical expression is associated with good prognostic factors of urothelial carcinoma (UC).
  • Positive CD36 immunohistochemical expression is associated with poor prognostic factors of UC.
  • High TIPE2 immunostaining is associated with negative vimentin expression.
  • High CD36 immunostaining is associated with positive vimentin expression.
  • The current results suggest that TIPE2 and CD36 may influence UC metastasis through epithelial-mesenchymal transition.
  • Negative TIPE2 and positive CD36 immunostaining may be beneficial tools for predicting cancer aggressiveness and metastasis and detecting outcomes of UC. They may also serve as potential therapeutic targets.

Keywords

Subjects


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Volume 20, Issue 1
Winter 2025
Pages 58-67

  • Receive Date 25 May 2024
  • Revise Date 19 July 2024
  • Accept Date 07 November 2024