重编程
表观遗传学
胶质母细胞瘤
磷酸肌酸
生物
遗传学
癌症研究
基因
内分泌学
能量代谢
作者
Lishu Chen,Qinghui Qi,Xiaoqing Jiang,Jin Wu,Yuanyuan Li,Zhaodan Liu,Yan Cai,Haowen Ran,Songyang Zhang,Cheng Zhang,Huiran Wu,Shuailiang Cao,Lanjuan Mi,Dake Xiao,Haohao Huang,Shuai Jiang,Jiaqi Wu,Bohan Li,Jiong Xie,Ji Qi
标识
DOI:10.1158/2159-8290.28124048
摘要
<p>Supplementary Figures S1 shows that GSCs produce high levels of phosphocreatine through upregulating CKB. Supplementary Figures S2 shows that ZEB1 promotes CKB transcription in GSCs. Supplementary Figures S3 shows that knockdown of CKB impedes GBM growth. Supplementary Figures S4 shows that disruption of phosphocreatine production impedes GBM growth. Supplementary Figures S5 shows that cCr treatment shows no side effect on mice. Supplementary Figures S6 shows that phosphocreatine binds to BRD2 and inhibits its ubiquitin mediated proteasomal degradation. Supplementary Figures S7 shows that phosphocreatine promotes chromosome segregation and GSC proliferation through BRD2 mediated transcription. Supplementary Figures S8 shows that disruption of phosphocreatine biosynthesis by cCr improves JQ1 therapeutic efficacy in GBM.</p>
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