Role of AT-rich interaction domain 1A in gastric cancer immunotherapy: Preclinical and clinical perspectives.
Xuemei ZhangYouzhi ZhangQiaoyun ZhangMengyao LuYuan ChenXiao-Yu ZhangPeng ZhangPublished in: Journal of cellular and molecular medicine (2023)
The application of immune checkpoint inhibitor (ICI) using monoclonal antibodies has brought about a profound transformation in the clinical outcomes for patients grappling with advanced gastric cancer (GC). Nonetheless, despite these achievements, the quest for effective functional biomarkers for ICI therapy remains constrained. Recent research endeavours have shed light on the critical involvement of modified epigenetic regulators in the pathogenesis of gastric tumorigenesis, thus providing a glimpse into potential biomarkers. Among these regulatory factors, AT-rich interaction domain 1A (ARID1A), a pivotal constituent of the switch/sucrose non-fermentable (SWI/SNF) complex, has emerged as a promising candidate. Investigations have unveiled the pivotal role of ARID1A in bridging the gap between genome instability and the reconfiguration of the tumour immune microenvironment, culminating in an enhanced response to ICI within the landscape of gastric cancer treatment. This all-encompassing review aims to dissect the potential of ARID1A as a valuable biomarker for immunotherapeutic approaches in gastric cancer, drawing from insights garnered from both preclinical experimentation and clinical observations.
Keyphrases
- end stage renal disease
- transcription factor
- newly diagnosed
- ejection fraction
- stem cells
- cell therapy
- gene expression
- prognostic factors
- genome wide
- squamous cell carcinoma
- intellectual disability
- risk assessment
- autism spectrum disorder
- bone marrow
- lymph node
- mesenchymal stem cells
- mass spectrometry
- climate change
- human health
- gas chromatography
- tandem mass spectrometry