Target intelligence / Profile preview

Acylphosphatase 1 (ACYP1)

Target
ACYP1
Molecular classification
Enzyme
01

Overview

Acylphosphatase 1 (ACYP1) is a small cytosolic enzyme found in vertebrate tissues, most notably in erythrocytes, where it catalyzes the hydrolysis of acylphosphates, breaking the carboxyl-phosphate bond. This enzymatic activity plays a key role in regulating glycolytic flux, membrane ion pump activity, and broader metabolic processes. ACYP1 influences multiple physiological processes including cellular differentiation, senescence, and metabolic adaptation. It is implicated in several disease states, most prominently as a prognostic biomarker of poor outcome in various cancers such as hepatocellular carcinoma, gastric cancer, and gastrointestinal tumors. Increased ACYP1 expression is associated with tumor progression, immune cell infiltration (such as Th2, Tregs, dendritic cells, macrophages), and cancer-related metabolic reprogramming. Although not presently a common direct drug target, its metabolic and immunological roles make it a candidate for therapeutic exploration in oncology and metabolic disorders[1][2][3].

Other names
Acylphosphatase-1ACYPEAcylphosphatase, erythrocyte isozymeAcylphosphate phosphohydrolase 1Acylphosphatase, organ-common type isozymeacylphosphatase-1, erythrocyte (common) type
02

Mechanism of action

No well-established mechanism of action for drugs specifically targeting ACYP1; role in resistance to imatinib in GIST suggests indirect modulation of drug sensitivity Broadly, inhibition or modulation could influence cancer metabolism and immune cell infiltration

03

Biological functions

Hydrolysis of acylphosphates, especially the carboxyl-phosphate bondRegulation of glycolysisMetabolic regulationModulation of membrane ion pump activityRole in erythrocyte senescenceRegulation of cell differentiationRegulation of intracellular calcium homeostasis
04

Disease associations

Cancer (general, pancancer, especially liver hepatocellular carcinoma, gastrointestinal cancer, cholangiocarcinoma, gastric cancer, colon cancer, glioblastoma)Involvement in imatinib resistance in gastrointestinal stromal tumorsNiemann–Pick disease, type C1Dialysis-related amyloidosis
05

Safety considerations

Modulation may impact metabolic pathways, immune function, and erythrocyte physiology due to essential roles in metabolism and ion transport—therapeutic challenges in specificity and toxicity may occur
06

Interacting drugs

07

Biomarkers

Prognostic biomarker for cancer progression, especially in liver hepatocellular carcinoma (LIHC), gastric and cholangiocarcinomaPrognostic indicator by expression level correlating to immune infiltration and survival

Beyond the preview

Go deeper on Acylphosphatase 1 (ACYP1).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Acylphosphatase 1 (ACYP1).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call