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AAAGUGC Seed-Containing miRNAs: Master Regulators of Cancer Pathways and Therapeutic Resistance
Chandhru Srinivasan1, Mano Chitra Karthikeyan1, Abirami Jeyaprakash1
1Department of Biochemistry, Molecular Oncology Laboratory, School of Life Sciences, Bharathidasan University, Tiruchirappalli, Tamil Nadu, 620 024, India.
Abstract:
MicroRNAs have emerged as pivotal post-transcriptional regulators, orchestrating a myriad of cellular processes critical to both normal physiology and pathological conditions, particularly cancer. Among these, miRNAs containing the highly conserved AAAGUGC seed sequence have garnered significant attention due to their multifaceted roles in cancer progression, acting as both oncogenes and tumour suppressors across a wide spectrum of malignancies. This review delves deeply into the evolutionary significance of AAAGUGC seed-containing miRNAs, elucidating their conserved nature and intricate roles in the regulation of cancer-related gene expression networks. We focused on eight specific miRNAs- miR-17-5p, miR-20a-5p, miR-93-5p, miR-106a-5p, miR-106b-5p, miR-519d-3p, miR-526b-3p, and miR-20b-5p -each of which demonstrates context-dependent oncogenic or tumour-suppressive behaviour. Through an indepth exploration of the molecular mechanisms by which these miRNAs modulate critical pathways, we highlighted their capacity to influence essential processes, including cell proliferation, apoptosis, epithelial-to-mesenchymal transition (EMT), metastasis, and drug resistance, reflecting the complexity of their regulatory roles. Furthermore, we dissected the intricate interactions between these miRNAs and their downstream targets, showcasing their diverse contributions to the tumour microenvironment. The implications of miRNA dysregulation in chemotherapy resistance were also explored. In conclusion, AAAGUGC seed-containing miRNAs represent a complex and evolutionarily conserved family with implications in cancer biology. Their ability to modulate multiple oncogenic and tumour-suppressive pathways highlights their potential as therapeutic targets or biomarkers in the context of personalized cancer treatment strategies. This review provides a comprehensive depth of current knowledge while proposing avenues for future research into the therapeutic manipulation of these miRNAs in combating cancer.
Insights
MicroRNAs with the AAAGUGC seed sequence are evolutionarily conserved regulators involved in cancer. These microRNAs (miRNAs) can act as oncogenes or tumor suppressors, influencing key cancer pathways and offering potential therapeutic targets.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- MicroRNAs (miRNAs) are key post-transcriptional regulators impacting cellular processes and diseases, especially cancer.
- miRNAs with the conserved AAAGUGC seed sequence play dual roles (oncogenic and tumor-suppressive) in various malignancies.
Purpose of the Study:
- To review the evolutionary significance and roles of AAAGUGC seed-containing miRNAs in cancer.
- To explore the molecular mechanisms and downstream targets of eight specific miRNAs in cancer progression.
Main Methods:
- Literature review focusing on AAAGUGC seed-containing miRNAs.
- Analysis of molecular mechanisms regulating cancer pathways like proliferation, apoptosis, EMT, metastasis, and drug resistance.
- Examination of miRNA interactions within the tumor microenvironment and their link to chemotherapy resistance.
Main Results:
- Eight specific miRNAs (miR-17-5p, miR-20a-5p, miR-93-5p, miR-106a-5p, miR-106b-5p, miR-519d-3p, miR-526b-3p, miR-20b-5p) exhibit context-dependent oncogenic or tumor-suppressive functions.
- These miRNAs modulate critical cancer-related cellular processes and interact with the tumor microenvironment.
- miRNA dysregulation is implicated in chemotherapy resistance.
Conclusions:
- AAAGUGC seed-containing miRNAs are evolutionarily conserved and complex regulators in cancer biology.
- Their ability to influence multiple pathways highlights their potential as therapeutic targets and biomarkers for personalized cancer treatment.
- Further research is needed for therapeutic manipulation of these miRNAs in cancer therapy.
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