ArticleDiscover oncology2025
hsa-miR-21-5p can serve as a standard biomarker in clear cell renal cell carcinoma by promoting tumor progression and influencing immune evasion.
Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Regulatory networks of non-coding RNAs in renal cell carcinogenesis and therapeutic intervention strategies.World journal of urology · 2026Review
- Multi-omics insights into tumor grade progression in clear cell renal cell carcinoma: from molecular mechanisms to precision therapeutics.Frontiers in cell and developmental biology · 2026Review
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Authors and funding
11 authors.
Funding
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Abstract
The increased expression of hsa-miR-21-5p in clear cell renal cell carcinoma (ccRCC) patients is closely linked to poor overall survival. Our predictive model, validated through tumor grading and staging, corresponds with enrichment analysis results and is further supported by PCR findings. Target gene predictions highlight the role of calcium ion transport and basement membrane functionality, with links to critical signaling pathways like JAK-STAT, cGMP-PKG, and sphingolipid, which play crucial roles in biological processes. Patients with higher levels of hsa-miR-21-5p show reduced responses to immunotherapy. In contrast, drug sensitivity analysis reveals increased vulnerability to drugs such as axitinib, sunitinib, and cabozantinib. This extensive investigation reveals the molecular complexities of ccRCC and suggests potential therapeutic options. In conclusion, upregulation of hsa-miR-21-5p in ccRCC is closely associated with tumor initiation and progression, indicating a poor prognosis. Its impact on the tumor microenvironment impairs the efficacy of immune therapies, contributing to adverse prognostic outcomes.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.