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Un-methylation of NUDT21 represses docosahexaenoic acid biosynthesis contributing to enzalutamide resistance in prostate cancer
Drug Resistance Updates ( IF 15.8 ) Pub Date : 2024-08-24 , DOI: 10.1016/j.drup.2024.101144
Shin-Chih Lin, Ya-Chuan Tsai, Ying-Lan Chen, Hui-Kuan Lin, Yun-Chen Huang, Yi-Syuan Lin, Yu-Sheng Cheng, Hsing-Yi Chen, Chia-Jung Li, Tsung-Yen Lin, Shih-Chieh Lin

The recent approval of enzalutamide for metastatic castration-sensitive prostate cancer underscores its growing clinical significance, raising concerns about emerging resistance and limited treatment options. While the reactivation of the androgen receptor (AR) and other genes plays a role in enzalutamide resistance, identifications of novel underlying mechanism with therapeutic potential in enzalutamide-resistant (EnzaR) cells remain largely elusive.

中文翻译:


NUDT21 的去甲基化抑制二十二碳六烯酸的生物合成,导致前列腺癌的恩杂鲁胺耐药



恩杂鲁胺最近被批准用于转移性去势敏感性前列腺癌,这凸显了其日益增长的临床意义,引发了人们对新出现的耐药性和有限治疗选择的担忧。虽然雄激素受体 (AR) 和其他基因的再激活在恩杂鲁胺耐药性中发挥作用,但在恩杂鲁胺耐药 (EnzaR) 细胞中确定具有治疗潜力的新潜在机制在很大程度上仍然难以捉摸。
更新日期:2024-08-24
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