Elevated expression of transferrin receptor-1 in pancreatic cancer: clinical implications and prognostic significance
- Li Zhongqing 1,2, Shahab Uddin 3, Zhou Wence 4,5
- Li Zhongqing 1,2, Shahab Uddin 3, Zhou Wence 4,5
- 1Department of General Surgery, The Second Hospital of Lanzhou University & The Second Clinical Medical School, Lanzhou University, Lanzhou, People's Republic of China.
- 2Gansu Province Hepatobiliary Pancreatic Disease Precision Diagnosis and Treatment Engineering Research Center, Cuiyingmen, Lanzhou, People's Republic of China.
- 3Institute of Microbiology, School of Life Sciences, Lanzhou University, Tianshui Road No. 222, Lanzhou, 730000, Gansu Province, People's Republic of China.
- 4Department of General Surgery, The Second Hospital of Lanzhou University & The Second Clinical Medical School, Lanzhou University, Lanzhou, People's Republic of China. zhouwc129@163.com.
- 5Gansu Province Hepatobiliary Pancreatic Disease Precision Diagnosis and Treatment Engineering Research Center, Cuiyingmen, Lanzhou, People's Republic of China. zhouwc129@163.com.
- 0Department of General Surgery, The Second Hospital of Lanzhou University & The Second Clinical Medical School, Lanzhou University, Lanzhou, People's Republic of China.
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View abstract on PubMed
Summary
This summary is machine-generated.High transferrin receptor-1 (TfR1) expression indicates poor outcomes in pancreatic cancer. This finding suggests TfR1 as a potential prognostic biomarker and therapeutic target for this fatal disease.
Area Of Science
- Oncology
- Molecular Biology
- Genetics
Background
- Pancreatic cancer, particularly advanced stages, has a poor prognosis, necessitating reliable prognostic indicators.
- Transferrin receptor-1 (TfR1) is a cell surface protein involved in iron uptake, with potential roles in cancer progression.
Purpose Of The Study
- To investigate the expression of TfR1 in pancreatic cancer tissues and cell lines.
- To evaluate the clinical and therapeutic potential of TfR1 as a prognostic biomarker in pancreatic cancer.
Main Methods
- Analysis of TFRC gene expression in pancreatic cancer and normal tissues using TCGA and GTEx data.
- Assessment of TfR1 protein levels in pancreatic cancer cell lines via Western blotting and immunofluorescence.
- Immunohistochemistry (IHC) staining of TfR1 in 90 patient tissue samples.
- Statistical analyses including ROC curves, Kaplan-Meier, Log-rank tests, and COX regression.
Main Results
- Significantly elevated TFRC mRNA levels in pancreatic cancer tissues compared to normal tissues (AUC = 0.936).
- Increased TfR1 protein expression observed in pancreatic cancer cell lines and patient tissues (30.1% vs 11.1% in paracancer).
- Higher TfR1 expression correlated with poorer overall survival (OS) and progression-free survival (PFS), identified as an independent prognostic factor.
Conclusions
- Elevated TfR1 expression is significantly associated with adverse outcomes in pancreatic cancer.
- TfR1 demonstrates potential as a valuable prognostic biomarker for pancreatic cancer.
- TfR1 may serve as a promising therapeutic target for pancreatic cancer treatment.
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