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Published on: May 30, 2025
The regulatory role of long non- coding RNAs as a novel controller of immune response against cancer cells
Dina Mofed1, Jihad I Omran1, Salwa Sabet2
1Molecular Biology and Virology lab, Biomedical Sciences Program, UST, Zewail City of Science and Technology, October Gardens, 6th of October City, 12578, Giza, Egypt.
Abstract:
Immunotherapy has been established as a promising therapy for different cancer types. However, many patients experience primary or secondary resistance to treatment. Immune cells and anti-inflammatory factors are regulated by long noncoding RNAs (lncRNAs). In addition, lncRNAs have a role in immune resistance through antigen presentation loss or attenuation, PD-L1 upregulation, loss of T-cell activities, and activation of G-MDSCs and Tregs in the tumor environment. LncRNAs can also influence the interaction between cancer stem cells and immune cells in the tumor microenvironment, potentially resulting in cancer stem cell resistance to immunotherapy. Immunological-related lncRNAs can influence immune responses either directly by affecting neighboring protein-coding genes or indirectly by sponging miRNAs through various mechanisms. We have emphasized the role and levels of expression of lncRNAs that have been linked to immune cell formation, differentiation, and activation, which may have an influence on immunotherapy efficacy.
Insights
Long noncoding RNAs (lncRNAs) regulate immune cells and influence immunotherapy resistance in cancer. Understanding lncRNA expression is key to overcoming treatment challenges.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Immunotherapy is a promising cancer treatment, but resistance remains a significant clinical challenge.
- Long noncoding RNAs (lncRNAs) are critical regulators of immune responses and inflammation.
- lncRNAs play multifaceted roles in the tumor microenvironment, impacting immune cell function and cancer progression.
Purpose of the Study:
- To explore the role of lncRNAs in modulating immune responses relevant to cancer immunotherapy.
- To investigate how lncRNAs contribute to primary and secondary resistance to cancer immunotherapy.
- To highlight the potential of immunological-related lncRNAs as biomarkers or therapeutic targets.
Main Methods:
- Review and synthesis of existing literature on lncRNAs and immunotherapy.
- Analysis of mechanisms by which lncRNAs affect immune cell function and tumor immune evasion.
- Examination of lncRNA involvement in cancer stem cell interactions within the tumor microenvironment.
Main Results:
- lncRNAs regulate immune cell differentiation, activation, and function.
- lncRNAs contribute to immunotherapy resistance via mechanisms like antigen presentation loss, PD-L1 upregulation, and altered T-cell activity.
- lncRNAs influence the tumor microenvironment by affecting myeloid-derived suppressor cells (G-MDSCs) and regulatory T cells (Tregs).
- lncRNAs impact cancer stem cell interactions, potentially leading to immunotherapy resistance.
Conclusions:
- lncRNAs are crucial regulators of the immune response in cancer and significantly influence immunotherapy efficacy.
- Targeting specific lncRNAs or modulating their expression may offer novel strategies to overcome immunotherapy resistance.
- Further research into immunological-related lncRNAs is warranted to develop more effective cancer treatments.
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