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Chromosome 8 open reading frame 76 (C8orf76)

Target
C8orf76
Molecular classification
Other (Protein of uncharacterized/unknown family), Putative transcription factor
01

Overview

Chromosome 8 open reading frame 76 (C8orf76) is a protein-coding, nuclear-localized gene that is preferentially expressed and amplified in a range of human cancers, including gastric and liver cancer[2][4][5]. It likely functions as a transcriptional regulator, with evidence indicating it contains zinc-finger DNA-binding domains and interacts with promoters of genes such as lncRNA DUSP5P1 (activating the MAPK/ERK signaling axis in gastric cancer) and SLC7A11 (involved in ferroptosis in liver cancer)[2][4]. C8orf76 expression promotes cell proliferation, cell-cycle progression, suppression of apoptosis, and metastatic capabilities in multiple tumor models. Its amplification or overexpression is associated with poor prognosis and serves as a potential biomarker for cancer progression. Despite its critical role in oncogenesis, C8orf76 is not currently a direct therapeutic target, and no drugs are known to interact with it[2][3][4][5][6].

Other names
Chromosome 8 open reading frame 76C8orf76Uncharacterized protein C8orf76FLJ14825
02

Mechanism of action

Not applicable, as there are no known drugs or therapies that directly target C8orf76.

03

Biological functions

Transcription regulation (binds DNA at promoters, especially of lncRNA and protein-coding genes, and regulates gene expression—e.g., DUSP5P1, SLC7A11)Cell cycle regulation (promotes G1/S phase progression, upregulates cyclin D1/D3 and CDK4, inhibits inhibitors like p18, p53)Cell proliferation and tumorigenesis (promotes proliferation, migration, invasion; suppresses apoptosis, enhances tumor growth/metastasis in gastric and other cancers)Regulation of ferroptosis (positively regulates SLC7A11 transcription involved in ferroptosis in liver cancer)Potential: immune modulation and mRNA modification (based on pan-cancer multi-omics analysis)
04

Disease associations

Cancer (notably gastric, liver, breast, and other cancers where it is often amplified or overexpressed)Other (possible tumor suppressor role in select cancers where downregulated, but this remains to be clarified)
05

Safety considerations

Not established, as direct targeting has not been reported; theoretical concerns could include essential regulatory roles in proliferation and apoptosis that might impact normal tissues
06

Interacting drugs

None reported in current literature or databases; C8orf76 is not an established pharmacological target
07

Biomarkers

C8orf76 DNA copy-number amplification and mRNA/protein overexpression serve as prognostic biomarkers in gastric, breast, and possibly other cancers, being associated with poor outcomes or more aggressive disease

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