Target intelligence / Profile preview

Apolipoprotein B-containing lipoprotein (ApoB-LP) (ApoB-LP)

Target
ApoB-LP
Molecular classification
Lipoprotein, Macromolecular complex, Lipid-protein assembly
01

Overview

Apolipoprotein B-containing lipoproteins represent a class of atherogenic particles, including VLDL, IDL, and LDL, each defined by the presence of one molecule of apolipoprotein B (ApoB-100 or ApoB-48) (StatPearls, 2023). These complexes are the primary vehicles for transporting hydrophobic lipids like cholesterol and triglycerides through the plasma to meet cellular energy and structural demands (NIH, 2022). From a clinical perspective, they are the central drivers of atherosclerotic cardiovascular disease (ASCVD), as their entrapment in the arterial wall initiates the inflammatory cascade leading to plaque formation (PubMed, 2021). Therapeutic strategies targeting these lipoproteins are the cornerstone of cardiovascular risk reduction, focusing on either decreasing hepatic production or accelerating clearance from the blood. Key drug classes include statins, which inhibit cholesterol biosynthesis, and PCSK9 inhibitors, which prolong the lifespan of the LDL receptor to enhance particle uptake (Journal of Lipid Research, 2020). Monitoring ApoB levels is increasingly recognized as a more accurate biomarker of cardiovascular risk than LDL-C alone, as it reflects the total number of atherogenic particles in circulation (Circulation, 2019).

Other names
ApoB-LPsNon-HDL lipoproteinsAtherogenic lipoproteinsApoB-containing particles
02

Mechanism of action

Therapeutic mechanisms include the inhibition of HMG-CoA reductase to reduce cholesterol synthesis and upregulate LDL receptors, inhibition of the NPC1L1 transporter to reduce cholesterol absorption, inhibition of PCSK9 to increase LDL receptor density, and direct inhibition of ApoB synthesis or lipoprotein assembly.

03

Biological functions

Lipid transportCholesterol homeostasisTriglyceride metabolismReceptor-mediated endocytosis
04

Disease associations

AtherosclerosisCoronary artery diseaseHyperlipidemiaFamilial hypercholesterolemiaPeripheral artery diseaseIschemic stroke
05

Safety considerations

Myopathy and rhabdomyolysisElevated liver enzymes (transaminitis)Potential for hepatic steatosis with assembly inhibitorsInjection site reactions with biologicsIncreased risk of new-onset type 2 diabetes
06

Interacting drugs

Atorvastatin

10 more in the full profile.

07

Biomarkers

Serum Apolipoprotein B (ApoB) concentrationLow-density lipoprotein cholesterol (LDL-C)Non-high-density lipoprotein cholesterol (non-HDL-C)Lipoprotein(a)

Beyond the preview

Go deeper on Apolipoprotein B-containing lipoprotein (ApoB-LP) (ApoB-LP).

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 Apolipoprotein B-containing lipoprotein (ApoB-LP) (ApoB-LP).

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