Combining EZH2 and HDAC inhibitors to target castration-resistant prostate cancers.

Combining EZH2 and HDAC inhibitors to target castration-resistant prostate cancers.
复制标题

DOI:
10.1371/journal.pbio.3002081
复制
发表时间:
2023-04
期刊:
影响因子:
9.8
通讯作者:
Easwaran, Hariharan
Easwaran, Hariharan
中科院分区:
生物学1区
文献类型:
--
作者:
Coulter, Jonathan B.;Easwaran, Hariharan

文献摘要

参考文献

被引文献

相似文献

去势抵抗性前列腺癌(CRPC)耐药性的发展涉及表观遗传途径。PLOS Biology上的一项新研究表明,靶向zeste同源物增强子2(EZH2)和组蛋白脱乙酰酶(HDAC)的联合治疗可能使CRPC对表观遗传和标准疗法敏感。去势抵抗性前列腺癌(CRPC)耐药性的发展涉及EZH2和HDAC的表观遗传途径。这篇文章探讨了PLOS Biology的一项研究,该研究表明,针对这些酶的联合表观遗传疗法可以激活细胞应激途径,这可能使CRPC对表观遗传疗法和标准疗法敏感。
Development of resistance in castration-resistant prostate cancer (CRPC) involves epigenetic pathways. A new study in PLOS Biology demonstrates that combined therapy targeting enhancer of zeste homolog 2 (EZH2) and histone deacetylases (HDACs) may sensitize CRPC to both epigenetic and standard therapies. Development of resistance in castration-resistant prostate cancer (CRPC) involves epigenetic pathways involving EZH2 and HDACs. This Primer explores a PLOS Biology study showing that combined epigenetic therapy targeting these enzymes can activate cellular stress pathways, which may sensitize CRPC to both epigenetic and standard therapies.
DOI: 10.1158/0008-5472.can-08-2216
发表时间: 2009-02-01
期刊: Cancer research
影响因子: 11.2
作者:
Welsbie DS;Xu J;Chen Y;Borsu L;Scher HI;Rosen N;Sawyers CL
通讯作者: Sawyers CL
DOI: 10.20517/cdr.2021.105
发表时间: 2022
期刊: Cancer drug resistance (Alhambra, Calif.)
影响因子: --
作者:
Biersack B;Nitzsche B;Höpfner M
通讯作者: Höpfner M
DOI: 10.1016/j.celrep.2018.11.035
发表时间: 2018-12-04
期刊: CELL REPORTS
影响因子: 8.8
作者:
Kim, Jung;Lee, Yongik;Yu, Jindan
通讯作者: Yu, Jindan
DOI: 10.1158/0008-5472.can-18-0941
发表时间: 2018-10-15
期刊: Cancer research
影响因子: 11.2
作者:
Xiao L;Tien JC;Vo J;Tan M;Parolia A;Zhang Y;Wang L;Qiao Y;Shukla S;Wang X;Zheng H;Su F;Jing X;Luo E;Delekta A;Juckette KM;Xu A;Cao X;Alva AS;Kim Y;MacLeod AR;Chinnaiyan AM
通讯作者: Chinnaiyan AM
DOI: 10.1038/s41388-021-01982-4
发表时间: 2021-09
期刊: Oncogene
影响因子: 8
作者:
Park SH;Fong KW;Mong E;Martin MC;Schiltz GE;Yu J
通讯作者: Yu J