Proteomics

Dataset Information

0

A549 cell treated with DDP+TSA vs DDP


ABSTRACT: analysis how HDAC inhibitior TSA increase cispkatin cytotoxicity

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture, Lung Parenchyma

DISEASE(S): Colon Cancer

SUBMITTER: Yang Zhou  

LAB HEAD: ZHOU YANG

PROVIDER: PXD052203 | Pride | 2024-06-23

REPOSITORIES: Pride

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Publications

Trichostatin A Promotes Cytotoxicity of Cisplatin, as Evidenced by Enhanced Apoptosis/Cell Death Markers.

Zhou Yang Y   Luo Qun Q   Zeng Fangang F   Liu Xingkai X   Han Juanjuan J   Gu Liangzhen L   Tian Xiao X   Zhang Yanyan Y   Zhao Yao Y   Wang Fuyi F  

Molecules (Basel, Switzerland) 20240603 11


Trichostatin A (TSA), a histone deacetylase (HDAC) inhibitor, promotes the cytotoxicity of the genotoxic anticancer drug cisplatin, yet the underlying mechanism remains poorly understood. Herein, we revealed that TSA at a low concentration (1 μM) promoted the cisplatin-induced activation of caspase-3/6, which, in turn, increased the level of cleaved PARP1 and degraded lamin A&C, leading to more cisplatin-induced apoptosis and G2/M phase arrest of A549 cancer cells. Both ICP-MS and ToF-SIMS measu  ...[more]

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