Pre-clinical and clinical importance of miR-21 in human cancers: Tumorigenesis, therapy response, delivery approaches and targeting agents
Abstract
The field of non-coding RNA (ncRNA) has made significant progress in understanding the pathogenesis of diseases and has broadened our knowledge towards their targeting, especially in cancer therapy. ncRNAs are a large family of RNAs with microRNAs (miRNAs) being one kind of endogenous RNA which lack encoded proteins. By now, miRNAs have been well-coined in pathogenesis and development of cancer. The current review focuses on the role of miR-21 in cancers and its association with tumor progression. miR-21 has both oncogenic and onco-suppressor functions and most of the experiments are in agreement with the tumor-promoting function of this miRNA. miR-21 primarily decreases PTEN expression to induce PI3K/Akt signaling in cancer progression. Overexpression of miR-21 inhibits apoptosis and is vital for inducing pro-survival autophagy. miR-21 is vital for metabolic reprogramming and can induce glycolysis to enhance tumor progression. miR-21 stimulates EMT mechanisms and increases expression of MMP-2 and MMP-9 thereby elevating tumor metastasis. miR-21 is a target of anti-cancer agents such as curcumin and curcumol and its down-regulation impairs tumor progression. Upregulation of miR-21 results in cancer resistance to chemotherapy and radiotherapy. Increasing evidence has revealed the role of miR-21 as a biomarker as it is present in both the serum and exosomes making them beneficial biomarkers for non-invasive diagnosis of cancer.
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miR-21 modulates the Wnt/β-catenin and STAT3 signaling pathways.
“This miRNA modulates essential oncogenic pathways, including the Wnt/β-catenin signaling pathway, which is crucial for cell proliferation and differentiation, and the STAT3 (Signal Transducer and Activator of Transcription 3) pathway, which plays a significant role in tumorigenesis and immune evasion [12].”
From miR-21 as a diagnostic and prognostic biomarker in glioma: tissue and serum expression analysis in a Pakistani cohort (2026) · cites this paper as [12]
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- Authors
- Hashemi, M., Mirdamadi, M. S. A., Talebi, Y., Khaniabad, N., Banaei, G., Daneii, P., Gholami, S., Ghorbani, A., Tavakolpournegari, A., Farsani, Z. M., Zarrabi, A., Nabavi, N., Zandieh, M. A., Rashidi, M., Taheriazam, A., Entezari, M., & Khan, H.
- Affiliations
- Islamic Azad University, Tehran (IR)
- Universitat Autònoma de Barcelona (ES)
- Istinye University (TR)
- University of British Columbia (CA)
- University of Tehran (IR)
- Mazandaran University of Medical Sciences (IR)
- Abdul Wali Khan University Mardan (PK)
- Corresponding author
- Rashidi, Mohsen
- Taheriazam, Afshin
- Entezari, Maliheh
- Khan, Haroon
- ORCID
- Venue
- Pharmacological Research
- Publisher
- Elsevier BV
- Published
- 2023-01
- Volume
- 187
- Pages
- 106568
- ISSN
- 1043-6618 (ISSN-L)
- OpenAlex
- W4309763967
- Cited by
- 153
- References
- 8
- Citations by year
- 2026: 38 · 2025: 62 · 2024: 41 · 2023: 12
- FWCI
- 3.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Pharmacological Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Keywords
- miR-21, microRNA, carcinogenesis, PTEN, PI3K/Akt signaling, apoptosis, autophagy, metabolic reprogramming, glycolysis, epithelial-mesenchymal transition, MMP-2, MMP-9, metastasis, curcumin, curcumol, chemoresistance, radiotherapy resistance, tumor markers, exosomes, serum biomarkers, non-invasive cancer diagnosis, microRNA delivery
- MeSH terms
- Clinical Relevance, Cell Transformation, Neoplastic, Humans, Neoplasms, Gene Expression Regulation, Neoplastic, Phosphatidylinositol 3-Kinases, MicroRNAs, Cell Line, Tumor, Cell Proliferation, Carcinogenesis
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