Chromatin remodeling-driven autophagy activation induces cisplatin resistance in oral squamous cell carcinoma.
Ontology highlight
ABSTRACT: It is still challenging to predict the efficacy of cisplatin-based therapy, particularly in relation to the activation of macroautophagy/autophagy in oral squamous cell carcinoma (OSCC). We studied the effect of selected chromatin remodeling genes on the cisplatin resistance and their interplay with autophagy in 3-dimensional tumor model and xenografts. We analyzed gene expression patterns in the cisplatin-sensitive UMSCC1, and a paired cisplatin-resistant UM-Cis cells. Many histone protein gene clusters involved in nucleosome assembly showed significant difference of expression. Gain- and loss-of-function analyses revealed an inverse correlation between cisplatin resistance and HIST1H3D expression, while a positive correlation was observed with HIST3H2A or HIST3H2B expression. In UM-Cis,
SUBMITTER: Oh SY
PROVIDER: S-EPMC11322550 | biostudies-literature | 2024 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA