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Publication : ARID1A mutations in cancer development: mechanism and therapy.

First Author  Zhang X Year  2023
Journal  Carcinogenesis Volume  44
Issue  3 Pages  197-208
PubMed ID  36882165 Mgi Jnum  J:336127
Mgi Id  MGI:7486402 Doi  10.1093/carcin/bgad011
Citation  Zhang X, et al. (2023) ARID1A mutations in cancer development: mechanism and therapy. Carcinogenesis 44(3):197-208
abstractText  AT-Rich Interaction Domain 1A (ARID1A) is an important SWItch/Sucrose Non-Fermentation (SWI/SNF) chromatin remodeling complex subunit, and its coding gene has a high mutation frequency in many cancers. Current studies have reported that ARID1A mutational status is correlated to cancer development, including cell proliferation, invasiveness, metastasis, and morphological alterations. ARID1A acts as a tumor suppressor, regulating gene transcription, participating in DNA damage response, and influencing tumor immune microenvironment and signaling pathways. The absence of ARID1A in cancer can lead to widespread dysregulation of gene expression in cancer initiation, promotion, and progression. For patients with ARID1A mutations, effective individualized treatment can improve the prognosis of patients. In this review, we aim to discuss the mechanism of ARID1A mutations in cancer development and explore the significance of discoveries for treatment.
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