Cancer Cells Employ Nuclear Caspase-8 to Overcome the p53-Dependent G2/M Checkpoint through Cleavage of USP28.
第一作者:
Ines,Müller
第一单位:
Experimental Dermatology, Department of Dermatology, TU-Dresden, Dresden 01307, Germany; Center for Regenerative Therapies Dresden, TU-Dresden, Dresden 01307, Germany.
作者:
医学主题词
抗肿瘤药(Antineoplastic Agents);细胞凋亡(Apoptosis);半胱氨酸天冬氨酸蛋白酶8(Caspase 8);细胞核(Cell Nucleus);细胞增殖(Cell Proliferation);抗药性, 肿瘤(Drug Resistance, Neoplasm);女(雌)性(Female);基因表达调控, 酶学(Gene Expression Regulation, Enzymologic);基因表达调控, 肿瘤(Gene Expression Regulation, Neoplastic);HCT116细胞(HCT116 Cells);人类(Humans);男(雄)性(Male);肿瘤(Neoplasms);蛋白质稳定性(Protein Stability);信号传导(Signal Transduction);肿瘤细胞, 培养的(Tumor Cells, Cultured);肿瘤抑制蛋白质p53(Tumor Suppressor Protein p53);泛素硫酯酶(Ubiquitin Thiolesterase)
DOI
10.1016/j.molcel.2019.12.023
PMID
31982308
发布时间
2023-11-13
基金项目
R01 AI044828/AI/NIAID NIH HHS/United States
R35 CA231620/CA/NCI NIH HHS/United States
R37 AI044828/AI/NIAID NIH HHS/United States
CIHR/Canada
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Molecular cell
970-984.e7页
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