Co-Targeting Nucleus Accumbens Associate 1 and NF-κB Signaling Synergistically Inhibits Melanoma Growth.
Lixiang GuXingcong RenChrispus M NguleXiaofang XiongJianxun SongZhiguo LiJin-Ming YangPublished in: Biomedicines (2023)
Nucleus-accumbens-associated protein-1 (NAC1) is a cancer-related transcriptional factor encoded by the NACC1 gene, which is amplified and overexpressed in various human cancers and has been appreciated as one of the top potential cancer driver genes. NAC1 has therefore been explored as a potential therapeutic target for managing malignant tumors. Here, we show that NAC1 is a negative regulator of NF-κB signaling, and NAC1 depletion enhances the level of the nuclear NF-κB in human melanoma. Furthermore, the inhibition of NF-κB signaling significantly potentiates the antineoplastic activity of the NAC1 inhibition in both the cultured melanoma cells and xenograft tumors. This study identifies a novel NAC1-NF-κB signaling axis in melanoma, offering a promising new therapeutic option to treat melanoma.
Keyphrases
- transcription factor
- signaling pathway
- lps induced
- genome wide analysis
- endothelial cells
- pi k akt
- genome wide identification
- nuclear factor
- oxidative stress
- genome wide
- inflammatory response
- skin cancer
- gene expression
- squamous cell carcinoma
- dna methylation
- immune response
- human health
- basal cell carcinoma
- cell proliferation
- heat shock