Related Experiment Video
Updated: Feb 23, 2026

13:19
Microarray-based Identification of Individual HERV Loci Expression: Application to Biomarker Discovery in Prostate Cancer
Published on: November 2, 2013
17.2K
TRAF2 is a Valuable Prognostic Biomarker in Patients with Prostate Cancer.
Bingbing Wei1, Jiabei Liang2, Jimeng Hu1
1Department of Urology, Huashan Hospital, Fudan University, Shanghai, China (mainland).
Summary
Tumor necrosis factor receptor-associated factor 2 (TRAF2) is upregulated in prostate cancer and predicts poorer recurrence-free survival. TRAF2 influences TRAIL-induced apoptosis, suggesting its potential as a prognostic biomarker.
Area of Science:
- Oncology
- Molecular Biology
Background:
- Tumor necrosis factor receptor-associated factor 2 (TRAF2) plays a role in cancer development and progression.
- Prostate cancer remains a significant health concern, necessitating improved prognostic markers.
Purpose of the Study:
- To evaluate TRAF2 as a prognostic biomarker in prostate cancer.
- To investigate TRAF2's role in regulating TRAIL-induced apoptosis in prostate cancer cells.
Main Methods:
- Utilized TCGA and GEO databases for gene expression analysis of TRAF2.
- Performed immunohistochemistry to assess TRAF2 protein levels in prostate cancer tissues.
- Employed Kaplan-Meier curves, log-rank tests, and Cox regression for survival analysis.
- Investigated TRAF2's effect on TRAIL-induced apoptosis in DU-145 cells.
Main Results:
- TRAF2 expression was significantly upregulated in prostate cancer compared to normal tissues and further elevated in metastatic disease.
- High TRAF2 expression correlated with advanced tumor stage and poorer recurrence-free survival.
- TRAF2 emerged as an independent prognostic factor for predicting recurrence-free survival.
- TRAF2 modulated TRAIL-induced apoptosis by regulating cleaved Caspase-8 and c-Flip expression.
Conclusions:
- TRAF2 is a promising novel prognostic biomarker for predicting recurrence-free survival in prostate cancer patients.
- TRAF2's association with prognosis may involve its regulation of TRAIL-induced apoptosis via the c-Flip/Caspase-8 signaling pathway.

