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Bioorg Med Chem ; 110: 117827, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-38964169

ABSTRACT

Histone deacetylase inhibitors (HDACis) show beneficial effects on different hematological malignancy subtypes. However, their impacts on treating solid tumors are still limited due to diverse resistance mechanisms. Recent studies have found that the feedback activation of BRD4-LIFR-JAK1-STAT3 pathway after HDACi incubation is a vital mechanism inducing resistance of specific solid tumor cells to HDACis. This review summarizes the recent development of multi-target HDACis that can concurrently block BRD4-LIFR-JAK1-STAT3 pathway. Moreover, our findings hope to shed novel lights on developing novel multi-target HDACis with reduced BRD4-LIFR-JAK1-STAT3-mediated drug resistance in some tumors.


Subject(s)
Histone Deacetylase Inhibitors , Janus Kinase 1 , Neoplasms , STAT3 Transcription Factor , Signal Transduction , Transcription Factors , Humans , STAT3 Transcription Factor/antagonists & inhibitors , STAT3 Transcription Factor/metabolism , Signal Transduction/drug effects , Histone Deacetylase Inhibitors/pharmacology , Histone Deacetylase Inhibitors/chemistry , Histone Deacetylase Inhibitors/chemical synthesis , Transcription Factors/antagonists & inhibitors , Transcription Factors/metabolism , Neoplasms/drug therapy , Neoplasms/metabolism , Neoplasms/pathology , Janus Kinase 1/antagonists & inhibitors , Janus Kinase 1/metabolism , Antineoplastic Agents/pharmacology , Antineoplastic Agents/chemistry , Antineoplastic Agents/chemical synthesis , Cell Cycle Proteins/antagonists & inhibitors , Cell Cycle Proteins/metabolism , Bromodomain Containing Proteins
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