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Updated: May 27, 2026

Synthesis and Characterization of an Aspirin-fumarate Prodrug that Inhibits NFκB Activity and Breast Cancer Stem Cells
Published on: January 18, 2017
NF-κB signaling in prostate cancer: a promising therapeutic target?
Garima Jain1, Marcus V Cronauer, Mark Schrader
1Institute of Pathology, University of Ulm, Albert-Einstein-Allee 23, 89070, Ulm, Germany.
Abstract:
Prostate carcinoma (PCa) displays a wide variety of genetic alterations, versatile expression profiles as well as cell surface markers. Despite this heterogeneity, a common treatment for advanced PCa is androgen deprivation therapy (ADT). ADT targets the androgen receptor-a member of the nuclear receptor superfamily-which is required for development and function of the prostate and critical for PCa growth and survival. After an initial regression of the tumor during ADT, a large fraction of tumors progress to so-called castration-resistant prostate carcinoma (CRPca) which is highly resistant toward chemotherapy. The ensuing high mortality rates illustrate the importance of novel therapeutic targets for CRPCa. The transcription factor NF-κB was recently proposed as such a potential target for therapeutic intervention in CRPCa. Although NF-κB is essential for the regulation of innate and adaptive immunity recent data suggest a role of NF-κB in cancer initiation and progression. However, the exact function of NF-κB signaling in PCa is still a matter of debate. Here, we review known roles of NF-κB signaling in PCa and emphasize the crosstalk of NF-κB and androgen receptor signaling. Finally, we discuss potential therapeutic relevance of blocking NF-κB in PCa.
Insights
This review explores the role of Nuclear Factor-kappa B (NF-κB) signaling in prostate carcinoma (PCa) progression, particularly in castration-resistant PCa (CRPCa). Targeting NF-κB may offer new therapeutic strategies for advanced prostate cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Prostate carcinoma (PCa) is heterogeneous, often treated with androgen deprivation therapy (ADT).
- Tumors frequently progress to castration-resistant prostate carcinoma (CRPCa), a chemotherapy-resistant stage with high mortality.
- Nuclear Factor-kappa B (NF-κB) signaling is implicated in cancer but its role in PCa remains debated.
Purpose of the Study:
- To review the known functions of NF-κB signaling in prostate carcinoma.
- To highlight the interplay between NF-κB and androgen receptor signaling in PCa.
- To discuss the therapeutic potential of inhibiting NF-κB in CRPCa.
Main Methods:
- Literature review of existing studies on NF-κB and prostate cancer.
- Analysis of the crosstalk between NF-κB and androgen receptor pathways.
- Discussion of therapeutic implications for NF-κB inhibition.
Main Results:
- NF-κB signaling plays a complex role in PCa initiation and progression.
- Significant crosstalk exists between NF-κB and androgen receptor signaling pathways.
- Emerging evidence suggests NF-κB as a potential therapeutic target for CRPCa.
Conclusions:
- NF-κB signaling is a critical factor in prostate cancer development and resistance to therapy.
- Understanding the NF-κB and androgen receptor interaction is key to developing effective treatments.
- Targeting NF-κB presents a promising avenue for novel therapeutic interventions in advanced prostate cancer.
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