Proteomics

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Deacetylation Induced Nuclear Condensation of HP1γ Promotes Multiple Myeloma Drug Resistance


ABSTRACT: Functional crosstalk between histone modifications and chromatin remodeling has emerged as a key regulatory mode of transcriptional control during drug resistance, but the underlying mechanisms are not fully understood. Here we demonstrate that different proteins and their acetylation modification regulate the resistance of multiple myeloma cells to BTZ.

ORGANISM(S): Homo Sapiens

SUBMITTER: Zhiqiang Liu  

PROVIDER: PXD040298 | iProX | Mon Feb 20 00:00:00 GMT 2023

REPOSITORIES: iProX

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Deacetylation induced nuclear condensation of HP1γ promotes multiple myeloma drug resistance.

Li Xin X   Wang Sheng S   Xie Ying Y   Jiang Hongmei H   Guo Jing J   Wang Yixuan Y   Peng Ziyi Z   Hu Meilin M   Wang Mengqi M   Wang Jingya J   Li Qian Q   Wang Yafei Y   Liu Zhiqiang Z  

Nature communications 20230309 1


Acquired chemoresistance to proteasome inhibitors is a major obstacle in managing multiple myeloma but key regulators and underlying mechanisms still remain to be explored. We find that high level of HP1γ is associated with low acetylation modification in the bortezomib-resistant myeloma cells using SILAC-based acetyl-proteomics assay, and higher HP1γ level is positively correlated with poorer outcomes in the clinic. Mechanistically, elevated HDAC1 in the bortezomib-resistant myeloma cells deace  ...[more]

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