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Is NF-kappaB a good target for cancer therapy? Hopes and pitfalls
Véronique Baud1, Michael Karin
1Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), 75014, Paris, France. veronique.baud@inserm.fr
Abstract:
Nuclear factor kappaB (NF-kappaB) transcription factors have a key role in many physiological processes such as innate and adaptive immune responses, cell proliferation, cell death, and inflammation. It has become clear that aberrant regulation of NF-kappaB and the signalling pathways that control its activity are involved in cancer development and progression, as well as in resistance to chemotherapy and radiotherapy. This article discusses recent evidence from cancer genetics and cancer genome studies that support the involvement of NF-kappaB in human cancer, particularly in multiple myeloma. The therapeutic potential and benefit of targeting NF-kappaB in cancer, and the possible complications and pitfalls of such an approach, are explored.
Insights
Nuclear factor kappaB (NF-kappaB) is crucial for cell functions but its dysregulation drives cancer. Targeting NF-kappaB shows therapeutic promise in multiple myeloma, despite potential complications.
Area of Science:
- Molecular Biology
- Cancer Research
- Immunology
Background:
- Nuclear factor kappaB (NF-kappaB) transcription factors regulate critical physiological processes including immune responses, cell proliferation, and inflammation.
- Aberrant regulation of NF-kappaB signaling pathways is implicated in the development, progression, and treatment resistance of various cancers.
- Multiple myeloma serves as a key example where NF-kappaB involvement is increasingly evident.
Purpose of the Study:
- To review recent evidence linking NF-kappaB to human cancer, with a focus on multiple myeloma.
- To explore the therapeutic potential and benefits of targeting NF-kappaB in cancer treatment.
- To discuss potential complications and challenges associated with NF-kappaB-targeted therapies.
Main Methods:
- Review of recent findings from cancer genetics studies.
- Analysis of cancer genome data.
- Synthesis of evidence on NF-kappaB pathway dysregulation in human cancers.
- Evaluation of therapeutic strategies targeting NF-kappaB.
Main Results:
- Cancer genetics and genome studies provide strong support for NF-kappaB's role in human cancer.
- NF-kappaB dysregulation is a significant factor in multiple myeloma pathogenesis.
- Targeting NF-kappaB presents a promising therapeutic avenue for cancer treatment.
- Potential pitfalls and complications of NF-kappaB-targeted therapies are identified.
Conclusions:
- NF-kappaB transcription factors are integral to cellular processes, and their aberrant activity drives cancer development and progression.
- Evidence from cancer genetics strongly implicates NF-kappaB in human malignancies, notably multiple myeloma.
- Targeting NF-kappaB offers significant therapeutic potential for cancer, but careful consideration of associated complications is necessary.
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