棕榈酰化
谷氨酰胺
化学
细胞生物学
新陈代谢
HEK 293细胞
下调和上调
细胞内
A549电池
生物化学
机制(生物学)
细胞生长
磷酸化
细胞代谢
信号转导
癌症研究
降级(电信)
细胞
蛋白质降解
作者
Xingyu Chen,Zihao Ke,Shihui Wei,Jiajin Chen,Ke Zhu,Jiaqi Xu,Yun Zhao,M. Cen,Yan Jin,Zhilei Pan,Juan Xiong,Ying Chen,Chenfang Dong,Qianhua Cao,Chao Cao
标识
DOI:10.1038/s41421-026-00870-z
摘要
S-palmitoylation, a reversible post-translational modification regulates protein stability and cellular functions, yet its role in glutamine metabolism remains unclear. Here, we show that ZDHHC14 as the key palmitoyltransferase catalyzing ASCT2 palmitoylation at conserved Cys39 and Cys48 residues, promoting lysosomal degradation of this glutamine transporter, whereas ABHD17B functions as a depalmitoylase to stabilize ASCT2. Mechanistically, glutamine deprivation activates JNK1, which directly phosphorylates ZDHHC14 at Thr440 residue, triggering its degradation and thereby enhancing ASCT2 stability. Importantly, combination of JNK and ASCT2 inhibitors synergistically inhibits glutamine metabolism and tumor growth in vivo. These findings reveal a phosphorylation-palmitoylation axis linking JNK-mediated ASCT2 palmitoylation and glutamine metabolism, offering a potential therapeutic strategy for non-small cell lung cancer.
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