Target intelligence / Profile preview

Pancreatic secretory granule membrane major glycoprotein 2 (GP2)

Target
GP2
Molecular classification
Other (Integral membrane glycoprotein), Transcytotic receptor (intestinal M cell), Zymogen granule membrane protein
01

Overview

Pancreatic secretory granule membrane major glycoprotein 2 (GP2) is an integral glycoprotein primarily expressed in the zymogen granules of pancreatic acinar cells and on the apical surface of intestinal M cells[3][5][6]. Upon stimulation, it is secreted into the pancreatic duct and intestine, where it plays a key role in antibacterial defense by binding bacterial adhesins, especially those with mannose-specific FimH (type I-piliated bacteria)[1][5][8]. GP2 acts as a decoy receptor, inhibiting bacterial adhesion to the intestinal mucosa and facilitating mucosal immune response by mediating bacterial transcytosis in M cells, leading to immune surveillance and IgA production[5][8]. GP2 is structurally related to UMOD (uromodulin/Tamm-Horsfall protein) and shares a zona pellucida (ZP) domain[1][5]. Genetic variants in GP2 are associated with susceptibility to pancreatic cancer[6]. It is used as a specific biomarker for the acinar cell lineage in the pancreas and has emerging utility as a plasma biomarker in diseases such as pancreatitis and pancreatic cancer[2][4][7]. Currently, GP2 is not a direct therapeutic target and no drugs or targeted mechanisms of action are described for it[2][4][6].

Other names
Glycoprotein 2Pancreatic zymogen granule membrane protein GP-2Pancreatic secretory granule membrane major glycoprotein GP2ZAP75Glycoprotein 2 (zymogen granule membrane)Pancreatic zymogen granule membrane associated protein GP2
02

Biological functions

Antibacterial defense in the gastrointestinal tract[1][6]Mucosal immune response/immune surveillance[5][6][8]Intracellular sorting, storage, and secretion of digestive enzymes[6]Transcytosis of bacteria by intestinal M cells[5][8]
03

Disease associations

Cancer (notably pancreatic cancer risk, some role in prostate cancer and other tumors)[2][6]Infection (role in bacterial adhesion and mucosal immunity)[1][5][8]Inflammation (expression in certain inflammatory states, e.g., Crohn’s disease M cells)[5]
04

Safety considerations

No data suggesting direct safety concerns or therapeutic challenges; GP2 is not a current drug target[2][4][6]
05

Biomarkers

Biomarker for acinar cell component in pancreatic tissue[2][7]Potential plasma marker for pancreatitis and pancreatic cancer[4]

Beyond the preview

Go deeper on Pancreatic secretory granule membrane major glycoprotein 2 (GP2).

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 Pancreatic secretory granule membrane major glycoprotein 2 (GP2).

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