TY - JOUR
T1 - Co-Targeting Nucleus Accumbens Associate 1 and NF-κB Signaling Synergistically Inhibits Melanoma Growth
AU - Gu, Lixiang
AU - Ren, Xingcong
AU - Ngule, Chrispus
AU - Xiong, Xiaofang
AU - Song, Jianxun
AU - Li, Zhiguo
AU - Yang, Jin Ming
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/8
Y1 - 2023/8
N2 - 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.
AB - 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.
KW - NAC1
KW - melanoma
UR - http://www.scopus.com/inward/record.url?scp=85168911833&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85168911833&partnerID=8YFLogxK
U2 - 10.3390/biomedicines11082221
DO - 10.3390/biomedicines11082221
M3 - Article
AN - SCOPUS:85168911833
VL - 11
JO - Biomedicines
JF - Biomedicines
IS - 8
M1 - 2221
ER -