MicroRNA-122 in human cancers: from mechanistic to clinical perspectives
Open accessAbstract
MicroRNAs (miRNAs) are endogenous short non-coding RNAs that can regulate the expression of target genes post-transcriptionally and interact with mRNA-coding genes. MiRNAs play vital roles in many biological functions, and abnormal miRNA expression has been linked to various illnesses, including cancer. Among the miRNAs, miR-122, miR-206, miR-21, miR-210, miR-223, and miR-424 have been extensively studied in various cancers. Although research in miRNAs has grown considerably over the last decade, much is yet to be discovered, especially regarding their role in cancer therapies. Several kinds of cancer have been linked to dysregulation and abnormal expression of miR-122, indicating that miR-122 may serve as a diagnostic and/or prognostic biomarker for human cancer. Consequently, in this review literature, miR-122 has been analyzed in numerous cancer types to sort out the function of cancer cells miR-122 and enhance patient response to standard therapy.
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The three selected miRNAs-hsa-miR-122-5p, hsa-let-7a-5p, and hsa-miR-26a-5p-provide complementary and comprehensive coverage of almost all critical genes associated with the MAPK signaling pathway.
“From this analysis, we selected the three abundant miRNAs-hsa-miR-122-5p, hsa-let-7a-5p, and hsa-miR26a-5p-based on their complementary and comprehensive coverage of almost all the critical genes associated with the MAPK signaling pathway 27-33 as analyzed using miRTarBase version 8.0 and TarBase v8.0 integrated within miRNet (Figure S1).”
From rAAV-mediated Multi-miRNA Delivery Targeting MAPK Pathway Suppresses Laser-induced Choroidal Neovascularization in Mice (2026) · cites this paper as [33]
The section “Mechanism of miR-122 in human cancers > Reproductive system” reports that miR-122-5p acts through MAPK signaling in triple-negative breast cancer. It does not assess the three-miRNA combination or show that they collectively cover almost all critical MAPK-pathway genes; the citing sentence describes that coverage as the citing authors’ own analysis. (LLM, conf=0.86)
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- Authors
- Faramin Lashkarian, M., Hashemipour, N., Niaraki, N., Soghala, S., Moradi, A., Sarhangi, S., Hatami, M., Aghaei-Zarch, F., Khosravifar, M., Mohammadzadeh, A., Najafi, S., Majidpoor, J., Farnia, P., & Aghaei-Zarch, S. M.
- Affiliations
- Yazd University (IR)
- Shahid Beheshti University (IR)
- Islamic Azad University, Tehran (IR)
- Kerman University of Medical Sciences (IR)
- University of Pennsylvania (US)
- Gonabad University of Medical Sciences (IR)
- Masih Daneshvari Hospital (IR)
- Corresponding author
- Aghaei-Zarch, Fatemehsadat
- Najafi, Sajad
- Majidpoor, Jamal
- Farnia, Poopak
- ORCID
- Venue
- Cancer Cell International
- Published
- 2023-02-20
- Volume
- 23
- Issue
- 1
- Pages
- 29-29
- ISSN
- 1475-2867 (ISSN-L)
- PMC
- PMC9940444
- OpenAlex
- W4321371253
- Cited by
- 105
- References
- 121
- Citations by year
- 2026: 9 · 2025: 36 · 2024: 30 · 2023: 30
- FWCI
- 3.35
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Cancer Cell International (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- 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-122, microRNA, cancer, post-transcriptional regulation, microRNA dysregulation, diagnostic biomarkers, prognostic factors, cancer therapy response, miR-21, miR-210, miR-223, miR-424, miR-206
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