Target intelligence / Profile preview

Pre-mRNA processing factor 4 kinase (PRP4K)

Target
PRP4K
Molecular classification
Enzyme, Serine/threonine kinase, CDK-like kinase (cyclin-dependent kinase-like), MAPK-related kinase, Splicing factor-associated kinase
01

Overview

Pre-mRNA processing factor 4 kinase (PRP4K) is a highly conserved, essential serine/threonine kinase involved in the phosphorylation of core spliceosomal proteins to facilitate formation and activation of the spliceosome B complex during pre-mRNA splicing[1][2][3][5]. Beyond splicing, PRP4K coordinates additional cell functions including regulation of transcription (through chromatin remodeling complexes), control of the spindle assembly checkpoint and cell division, and negative regulation of oncogenic YAP signaling. PRP4K acts as a tumor suppressor; its reduction or haploinsufficiency confers cancer cell resistance to taxane chemotherapy and promotes more aggressive disease, particularly in breast and ovarian cancer, making it a potential biomarker for drug response and prognosis[1]. PRP4K’s broad cellular roles, including links to neurodegeneration and sensitivity to mitotic stress, highlight its central role in genome maintenance and cell fate regulation[1][3].

Other names
PRPF4BPRP4Serine/threonine-protein kinase PRP4 homologpre-mRNA processing factor 4BPR4H
02

Mechanism of action

Not applicable (no direct drug targeting described); as a kinase, mechanistic rationale for inhibition would be to block phosphorylation of splicing and checkpoint proteins to affect mitosis or splicing in cancer cells[1][3]

03

Biological functions

Pre-mRNA splicingPhosphorylation of spliceosomal proteins (e.g., PRPF6, PRPF31, SRSF1)Spliceosome B complex activationRegulation of transcriptionChromatin remodeling (via interaction with NCOR1 and SMARCA4/BRG1)Spindle assembly checkpoint controlRegulation of mitosis and chromosome segregationRegulation of YAP and Hippo signalingCell proliferation and survival controlTumor suppression
04

Disease associations

CancerChemoresistance (especially to taxanes)Neurodegenerative diseases (through regulation of ELK1 phosphorylation in diseases such as Alzheimer’s and Huntington’s)
05

Safety considerations

Essential enzyme in RNA splicing and cell division, so inhibition could cause widespread cellular toxicity and may impair normal cell division and gene expression[1]
06

Interacting drugs

None known as approved or marketed drugs directly targeting PRP4K (as of 2025); experimental inhibitors of splicing kinases exist, but no PRP4K-selective clinical drug is established[1][3][5]
07

Biomarkers

PRP4K expression loss is a prognostic and predictive biomarker for taxane resistance in breast and ovarian cancer[1]Low expression correlates with poor survival in several cancers[1]

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