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In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol
Published on: December 30, 2016
The role of FOXP3 in non-small cell lung cancer and its therapeutic potentials
Jia Peng1, Shucai Yang2, Calvin S H Ng1
1Department of Surgery, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Abstract:
Although in the last few decades we have witnessed the rapid development of treatments for non-small cell lung cancer (NSCLC), it still remains the leading cause of cancer-related death. Increasing efforts have been devoted to exploring potential biomarkers and molecular targets for NSCLC. Foxp3, a transcription factor that was discovered as a master regulator of regulatory T cells (Tregs), has been found to express abnormally in tumoral cells including lung cancer cells. In recent years, increasing evidence have surfaced, revealing the carcinogenic effect of FOXP3 in lung cancer. In this review, we analyzed and summarized the function of FOXP3, its regulation and therapeutic potentials in NSCLC, with a hope to facilitate the development of novel treatments for NSCLC.
Insights
Forkhead box protein P3 (FOXP3) shows abnormal expression in non-small cell lung cancer (NSCLC). This review explores FOXP3
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Non-small cell lung cancer (NSCLC) remains a leading cause of cancer mortality despite treatment advancements.
- Forkhead box protein P3 (FOXP3), a key regulator of regulatory T cells (Tregs), is aberrantly expressed in various tumor cells, including lung cancer.
- Emerging evidence suggests a carcinogenic role for FOXP3 in lung cancer development and progression.
Purpose of the Study:
- To review the multifaceted functions of FOXP3 in the context of NSCLC.
- To analyze the regulatory mechanisms governing FOXP3 expression in lung cancer.
- To explore the therapeutic potential of targeting FOXP3 for novel NSCLC treatments.
Main Methods:
- Comprehensive literature review of studies investigating FOXP3 in NSCLC.
- Analysis of existing data on FOXP3 expression patterns and functional roles.
- Synthesis of information regarding FOXP3 regulation and its implications for therapy.
Main Results:
- FOXP3 expression is dysregulated in NSCLC tumoral cells.
- FOXP3 exhibits a pro-tumorigenic effect in lung cancer.
- Understanding FOXP3's function and regulation is crucial for NSCLC research.
Conclusions:
- FOXP3 represents a significant molecular target for NSCLC intervention.
- Targeting FOXP3 may offer a novel therapeutic strategy for NSCLC patients.
- Further research into FOXP3's role can accelerate the development of effective NSCLC treatments.
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