NOVA1 acts as an oncogenic RNA-binding protein to regulate cholesterol homeostasis in human glioblastoma cells Journal Article


Authors: Saito, Y.; Yang, Y.; Saito, M.; Park, C. Y.; Funato, K.; Tabar, V.; Darnell, R. B.
Article Title: NOVA1 acts as an oncogenic RNA-binding protein to regulate cholesterol homeostasis in human glioblastoma cells
Abstract: NOVA1 is a neuronal RNA-binding protein identified as the target antigen of a rare autoimmune disorder associated with cancer and neurological symptoms, termed paraneoplastic opsoclonus-myoclonus ataxia. Despite the strong association between NOVA1 and cancer, it has been unclear how NOVA1 function might contribute to cancer biology. In this study, we find that NOVA1 acts as an oncogenic factor in a GBM (glioblastoma multiforme) cell line established from a patient. Interestingly, NOVA1 and Argonaute (AGO) CLIP identified common 3' untranslated region (UTR) targets, which were down-regulated in NOVA1 knockdown GBM cells, indicating a transcriptome-wide intersection of NOVA1 and AGO-microRNA (miRNA) targets regulation. NOVA1 binding to 3'UTR targets stabilized transcripts including those encoding cholesterol homeostasis related proteins. Selective inhibition of NOVA1-RNA interactions with antisense oligonucleotides disrupted GBM cancer cell fitness. The precision of our GBM CLIP studies point to both mechanism and precise RNA sequence sites to selectively inhibit oncogenic NOVA1-RNA interactions. Taken together, we find that NOVA1 is commonly overexpressed in GBM, where it can antagonize AGO2-miRNA actions and consequently up-regulates cholesterol synthesis, promoting cell viability.
Keywords: genetics; metabolism; microrna; cell line, tumor; rna binding protein; gene expression regulation; rna-binding proteins; gene expression regulation, neoplastic; glioblastoma; tumor cell line; cholesterol; micrornas; homeostasis; rna-binding protein; clip; humans; human; nova1; neuro-oncological ventral antigen; neuro oncological ventral antigen; nova1 protein, human
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 121
Issue: 10
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2024-03-05
Start Page: e2314695121
Language: English
DOI: 10.1073/pnas.2314695121
PUBMED: 38416679
PROVIDER: scopus
PMCID: PMC10927500
DOI/URL:
Notes: Source: Scopus
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  1. Viviane S Tabar
    225 Tabar
  2. Kosuke Funato
    14 Funato