Akademik Veri Yönetim Sistemi
DISCOVER ONCOLOGY, cilt.16, sa.1, 2025 (SCI-Expanded)
BackgroundOne of the major dilemmas in the treatment of renal cell carcinoma (RCC) is the resistance to therapy that leads to a state of unresponsiveness, which is observed after a certain period. Among the potential causes of this, the impact of autophagy activation and the resulting endoplasmic reticulum (ER) stress due to the accumulation of misfolded or unfolded proteins has not been previously investigated.MethodsPatients treated in medical oncology clinics of a total of 3 centers between January 2011 and May 2022 were included. In the pathology preparations of a total of 83 patients diagnosed with metastatic RCC, we examined the effects of autophagy activation induced by mTOR inhibition through the analysis of LC3 and Beclin1 molecules, the differentiation from classical apoptosis pathways with the Bcl-2 level, the hypoxic condition with the HIF-1 alpha level, and ER stress with the eukaryotic initiation factor 2 alpha (eIF2 alpha) level.Results & Idot;n our study, found no significant effects of LC3 (p = 0.298), Beclin1 (p = 0.287), Bcl-2 (p = 0.435), and HIF-1 alpha (p = 0.179) levels on either progression-free survival or overall survival. However, eIF2 alpha (p = 0.017) was found to be a significantly decisive factor.ConclusionBased on these results, we suggest that eIF2 alpha may serve as a novel biomarker to predict survival and treatment response in metastatic RCC patients.