mir 155 - Cancer Science

What is miR-155?

miR-155 is a type of microRNA, which are small non-coding RNAs that play critical roles in the regulation of gene expression. MicroRNAs function by binding to complementary sequences in the 3' untranslated regions (3'UTRs) of target messenger RNAs (mRNAs), leading to mRNA degradation or inhibition of translation.

How is miR-155 Linked to Cancer?

miR-155 has been identified as an oncogene in various types of cancers. Its overexpression is frequently observed in malignancies such as breast cancer, lung cancer, lymphoma, and leukemia. Elevated levels of miR-155 contribute to cancer progression by promoting cell proliferation, inhibiting apoptosis, and enhancing metastasis.

What Mechanisms are Involved?

miR-155 exerts its oncogenic effects through various mechanisms:
Regulation of Cell Cycle: miR-155 targets and downregulates the expression of key tumor suppressor genes such as SOCS1 (Suppressor of Cytokine Signaling 1) and TP53INP1 (Tumor Protein 53-Induced Nuclear Protein 1), leading to uncontrolled cell proliferation.
Inhibition of Apoptosis: miR-155 can inhibit apoptosis by targeting pro-apoptotic genes such as FOXO3a (Forkhead Box O3a) and BIM (Bcl-2-like 11).
Enhancement of Angiogenesis: miR-155 promotes angiogenesis by upregulating VEGF (Vascular Endothelial Growth Factor) and downregulating anti-angiogenic factors.
Modulation of Immune Response: miR-155 can alter immune surveillance by affecting the function of immune cells such as T cells and macrophages, contributing to an immunosuppressive tumor microenvironment.

What is the Clinical Significance of miR-155?

Given its pivotal role in cancer, miR-155 is being explored as a potential biomarker for cancer diagnosis, prognosis, and therapy. Elevated levels of miR-155 in blood or tissue samples can serve as an indicator of cancer presence and progression. Moreover, targeting miR-155 with anti-miR-155 molecules is being investigated as a therapeutic strategy to inhibit its oncogenic effects.

How Can miR-155 be Targeted for Therapy?

Several approaches are being developed to target miR-155 for cancer therapy:
Antisense Oligonucleotides (ASOs): These are short, synthetic strands of nucleic acids designed to bind to miR-155 and inhibit its function.
Locked Nucleic Acid (LNA) Inhibitors: LNAs are chemically modified nucleic acids with high affinity for their target miRNAs, providing potent and specific inhibition of miR-155.
Small Molecule Inhibitors: These compounds can interfere with miR-155 biogenesis or function, thereby reducing its oncogenic activity.
Nanoparticle Delivery Systems: Nanoparticles can be employed to deliver miR-155 inhibitors specifically to tumor cells, enhancing therapeutic efficacy and reducing off-target effects.

What Are the Challenges and Future Directions?

Despite the promising potential of targeting miR-155 for cancer therapy, several challenges remain:
Specificity: Ensuring that miR-155 inhibitors specifically target cancer cells without affecting normal cells is crucial to minimize side effects.
Delivery: Efficient delivery of miR-155 inhibitors to tumor sites while avoiding degradation in the bloodstream is a major hurdle.
Resistance: Cancer cells may develop resistance to miR-155 inhibitors, necessitating combination therapies and ongoing research to overcome this issue.
Future research is focused on improving delivery systems, understanding miR-155's role in different cancer types, and developing combination therapies that target multiple pathways involved in cancer progression.



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