Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12671
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dc.contributor.authorLi, J. J.-
dc.contributor.authorLee, C. S.-
dc.date.accessioned2024-03-11T01:57:51Z-
dc.date.available2024-03-11T01:57:51Z-
dc.date.issued2024-
dc.identifier.issn20734425 (ISSN)-
dc.identifier.urihttps://swslhd.intersearch.com.au/swslhdjspui/handle/1/12671-
dc.description.abstractThe switch/sucrose non-fermentable (SWI/SNF) (SWI/SNF) complex uses energy from ATP hydrolysis to mobilise nucleosomes on chromatin. Components of SWI/SNF are mutated in 20% of all human cancers, of which mutations in AT-rich binding domain protein 1A (ARID1A) are the most common. ARID1A is mutated in nearly half of ovarian clear cell carcinoma and around one-third of endometrial and ovarian carcinomas of the endometrioid type. This review will examine in detail the molecular functions of ARID1A, including its role in cell cycle control, enhancer regulation, and the prevention of telomerase activity. ARID1A has key roles in the maintenance of genomic integrity, including DNA double-stranded break repair, DNA decatenation, integrity of the cohesin complex, and reduction in replication stress, and is also involved in mismatch repair. The role of ARID1A loss in the pathogenesis of some of the most common human cancers is discussed, with a particular emphasis on gynaecological cancers. Finally, several promising synthetic lethal strategies, which exploit the specific vulnerabilities of ARID1A-deficient cancer cells, are briefly mentioned. � 2023 by the authors.-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.subjectARID1A BAF cancer SWI/SNF synthetic lethality tumour suppressor Carcinogenesis DNA DNA-Binding Proteins Female Humans Mutation Nuclear Proteins Ovarian Neoplasms Transcription Factors adenosine triphosphate BRCA2 protein epidermal growth factor receptor epidermal growth factor receptor kinase inhibitor estrogen receptor progesterone receptor telomerase transforming growth factor beta ARID1A protein, human DNA binding protein nuclear protein transcription factor angiogenesis apoptosis ARID1A gene breast carcinoma cancer growth cancer incidence cancer risk carcinogenicity cell cycle regulation cell differentiation cell infiltration cell proliferation chromatin clear cell carcinoma colorectal cancer colorectal carcinoma cytokine production cytotoxicity DNA methylation DNA repair double strand break repair double stranded DNA break endometrioid carcinoma endometrium carcinoma endometrium cell enhancer region epithelial mesenchymal transition gene gene expression gene interaction gene mutation gene silencing glycolysis HCT 116 cell line HEC-1-A cell line histology histone acetylation homologous recombination human hydrolysis immunohistochemistry lethality liver cell carcinoma lung adenocarcinoma microsatellite instability mismatch repair nonsense mutation nucleosome ovary cancer ovary carcinoma overall survival pancreas adenocarcinoma physiological stress Pi3K/Akt signaling PIK3CA gene prevalence protein domain Review somatic mutation stomach cancer telomere transitional cell carcinoma tumor growth tumor invasion tumor regression tumor suppressor gene tumor xenograft genetics metabolism ovary tumor pathology-
dc.titleThe Role of the AT-Rich Interaction Domain 1A Gene (ARID1A) in Human Carcinogenesis-
dc.typeJournal Article-
dc.contributor.swslhdauthorLi, Jing J.-
dc.contributor.swslhdauthorLee, Cheok S.-
dc.description.affiliatesDepartment of Anatomical Pathology, Liverpool Hospital, Liverpool, 2170, NSW, Australia Ingham Institute for Applied Medical Research, Liverpool, 2170, NSW, Australia Discipline of Pathology, School of Medicine, Western Sydney University, Sydney, 2560, NSW, Australia South Western Sydney Clinical School, University of New South Wales, Liverpool, 2170, NSW, Australia Department of Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Camperdown, 2010, NSW, Australia-
dc.identifier.doi10.3390/genes15010005-
dc.identifier.departmentLiverpool Hospital, Department of Anatomical Pathology-
dc.type.studyortrialReview-
dc.identifier.journaltitleGenes-
Appears in Collections:Liverpool Hospital

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