Target intelligence / Profile preview

Prenylated Rab acceptor 1 domain family member 2 (PRAF2)

Target
PRAF2
Molecular classification
Membrane transport protein, Endoplasmic reticulum (ER) associated protein, Vesicular trafficking protein, Other (not a canonical receptor, transporter, enzyme, or ion channel by classical criteria)
01

Overview

Prenylated Rab acceptor 1 domain family member 2 (PRAF2) is a four-transmembrane domain protein predominantly localized to the endoplasmic reticulum, implicated in vesicle-mediated protein trafficking from the ER to the Golgi apparatus[1][2]. PRAF2 is highly expressed in the brain, breast, lung, intestine, spleen, and pancreas, and is upregulated in several types of human cancers—including breast cancer, neuroblastoma, glioma, hepatocellular carcinoma, and esophageal carcinoma—where its elevated expression is often associated with increased tumor proliferation, migration, invasion, metastatic potential, and worse prognosis[1]. Biologically, PRAF2 participates in regulating cell proliferation, migration, and apoptotic processes, possibly through modulating Wnt/β-catenin signaling in some cancer contexts[1]. Though widely considered a promising therapeutic target and biomarker in oncology, no clinically approved drugs are currently known to selectively inhibit this protein[1][2].

Other names
PRA1 domain family member 2PRAF2JM4Yip6aJena-Muenchen 4PRA1 family protein 2Sfc20DXImx39e
02

Mechanism of action

no drugs targeting PRAF2; mechanism when considered as a target relates to inhibition of protein—gene knockdown studies reduce cancer cell proliferation and migration

03

Biological functions

Protein and vesicular transport between ER and GolgiRegulation of cell proliferation and migrationPro-apoptotic signaling in some contexts
04

Disease associations

Cancer (notably breast cancer, neuroblastoma, glioma, hepatocellular carcinoma, esophageal squamous cell carcinoma)Neurodegenerative disease (implicated in neuroblastoma pathophysiology)
05

Safety considerations

no direct pharmacological targeting or safety data; general concerns would be off-target effects on vesicular trafficking and essential cellular transport
06

Biomarkers

Overexpression is associated with poor prognosis in breast cancer, neuroblastoma, hepatocellular carcinoma, and esophageal squamous cell carcinomaPotential prognostic marker in these cancers

Beyond the preview

Go deeper on Prenylated Rab acceptor 1 domain family member 2 (PRAF2).

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 Prenylated Rab acceptor 1 domain family member 2 (PRAF2).

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