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Comprehensive Review: Unveiling the Pro-Oncogenic Roles of IL-1ß and PD-1/PD-L1 in NSCLC Development and Targeting
Dani Ran Castillo1, Won Jin Jeon2, Daniel Park3
1Division of Hematology and Oncology, Loma Linda University Cancer Center, Loma Linda, CA 92354, USA.
Interleukin-1 beta (IL-1β) shows promise as a therapeutic target for non-small cell lung cancer (NSCLC), especially for patients lacking targetable mutations. Combining IL-1β inhibitors with immune-checkpoint inhibitors may improve treatment outcomes.
Area of Science:
- Oncology
- Immunology
- Inflammation Biology
Background:
- Targeted therapies and immune-checkpoint inhibitors (ICIs) have advanced non-small cell lung cancer (NSCLC) treatment.
- Patients without targetable mutations or with limited response to ICIs present a clinical challenge.
- Programmed death ligand 1 (PD-L1) expression predicts ICI response, but new biomarkers in the tumor microenvironment (TME) are needed.
Purpose of the Study:
- To review the role of interleukin-1 beta (IL-1β) in NSCLC.
- To explore IL-1β's involvement in inflammatory pathways and its crosstalk with the PD-1/PD-L1 pathway.
- To investigate the potential of IL-1β as a therapeutic target for NSCLC.
Main Methods:
- Literature review on IL-1β, inflammation, PD-1/PD-L1 pathway, and NSCLC.
- Analysis of the relationship between IL-1β, oncogenesis, and cancer development.
- Exploration of combinatorial approaches involving IL-1β inhibitors and ICIs.
Main Results:
- IL-1β is implicated in NSCLC development and influences patient outcomes.
- The IL-1β/PD-1/PD-L1 pathway is a key area of focus for understanding inflammation in NSCLC.
- Combinatorial strategies targeting IL-1β and PD-1/PD-L1 may benefit patients lacking targetable mutations.
Conclusions:
- IL-1β plays a significant role in NSCLC and inflammatory processes.
- Targeting the IL-1β/PD-1/PD-L1 pathway offers potential for novel NSCLC treatments.
- Further research is needed to overcome treatment resistance associated with this pathway.
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