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Literature summary for 1.14.11.16 extracted from

  • Huang, C.K.; Iwagami, Y.; Zou, J.; Casulli, S.; Lu, S.; Nagaoka, K.; Ji, C.; Ogawa, K.; Cao, K.Y.; Gao, J.S.; Carlson, R.I.; Wands, J.R.
    Aspartate beta-hydroxylase promotes cholangiocarcinoma progression by modulating RB1 phosphorylation (2018), Cancer Lett., 429, 1-10 .
    View publication on PubMedView publication on EuropePMC

Organism

Organism UniProt Comment Textmining
Mus musculus Q8BSY0
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Synonyms

Synonyms Comment Organism
aspartate beta-hydroxylase
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Mus musculus
ASPH
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Mus musculus

General Information

General Information Comment Organism
drug target the enzyme (ASPH) may be a potential therapeutic target in CCA patients having the IDH1/2 wild-type genotype Mus musculus
malfunction knockdown of enzyme (ASPH) expression inhibits cholangiocarcinoma development and growth by reducing retinoblastoma protein (RB1) inhibition Mus musculus
physiological function the enzyme (ASPH) is involved in cholangiocarcinoma growth, progression and induction of cell senescence. The protein interaction between RB1 and the CDK complexes is modulated by ASPH expression Mus musculus