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Updated: Feb 13, 2026

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Analysis of Side Population in Solid Tumor Cell Lines
Published on: February 23, 2021
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Prognostic value of DcR3 in solid tumors: A meta-analysis
Hua Ge1, Chaojie Liang1, Shulin Ren1
1Department of general surgery, Beijing Tongren hospital, Capital Medical University, Beijing, People's Republic of China.
Summary
Increased expression of Decoy receptor 3 (DcR3) in solid tumors is linked to poorer overall survival for cancer patients. This suggests DcR3 is a potential biomarker for predicting cancer prognosis.
Area of Science:
- Oncology
- Molecular Biology
- Biomarker Discovery
Background:
- Decoy receptor 3 (DcR3) is frequently overexpressed in various solid tumors.
- This overexpression suggests a significant role for DcR3 in cancer development and progression.
Purpose of the Study:
- To evaluate the association between Decoy receptor 3 (DcR3) expression and patient prognosis in solid tumors.
- To synthesize existing evidence through a meta-analysis.
Main Methods:
- A comprehensive literature search was conducted across major scientific databases (PubMed, Web of Science, Cochrane Library, EMBASE, CNKI, Wan Fang).
- Pooled hazard ratios (HRs) for overall survival (OS) and recurrence-free survival (RFS) were calculated.
- Fixed and random effects models were employed for data analysis.
Main Results:
- Analysis of 16 studies involving 2209 patients revealed a significant correlation between DcR3 overexpression and worse overall survival (OS).
- However, DcR3 expression did not appear to be significantly related to recurrence-free survival (RFS) in the analyzed malignancies.
Conclusions:
- Elevated DcR3 expression is associated with poor prognosis in cancer patients.
- DcR3 expression status can serve as a valuable biomarker for predicting prognosis in patients with solid tumors.
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