Target intelligence / Profile preview

Esophageal neoplasia-associated cell surface markers

Molecular classification
Receptor tyrosine kinase, Cell adhesion molecule, Glycoprotein, Cell surface protein, Other
01

Overview

Esophageal neoplasia-associated cell surface markers refer to a heterogeneous collection of proteins and glycoproteins expressed on the outer membrane of cells during the development of esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC) [PubMed: 31435456]. These markers, which include the Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), and Claudin 18.2, play pivotal roles in driving oncogenic processes such as cell proliferation, survival, and metastasis [National Cancer Institute]. In the context of clinical oncology, these surface molecules are utilized as diagnostic tools and therapeutic targets for monoclonal antibodies, antibody-drug conjugates (ADCs), and CAR-T cell therapies [PubMed: 33808140]. For instance, Trastuzumab targets HER2-positive esophageal cancers, while newer agents like Zolbetuximab target Claudin 18.2 [ClinicalTrials.gov]. Because this term describes a broad category of distinct molecular entities rather than a single receptor or enzyme, it is typically used to define the surface proteome landscape of esophageal tumors for biomarker discovery [UniProt]. Consequently, while the individual components are valid therapeutic targets, the collective designation serves as a framework for multi-target diagnostic and therapeutic strategies.

Other names
Esophageal cancer surface antigensESCC surface markersEAC surface markersEsophageal tumor-associated antigensEsophageal cancer surface proteome
02

Mechanism of action

Inhibition of oncogenic signaling pathways, induction of antibody-dependent cellular cytotoxicity (ADCC), and targeted delivery of cytotoxic payloads to malignant cells.

03

Biological functions

Signal transductionCell proliferationCell adhesionSurvivalAngiogenesisOther
04

Disease associations

Esophageal squamous cell carcinomaEsophageal adenocarcinomaBarrett's esophagusCancer
05

Safety considerations

On-target off-tumor toxicities in healthy tissues expressing specific markersTherapeutic resistance via alternative signaling pathwaysInfusion-related reactionsCardiotoxicity (associated with HER2 inhibition)Dermatological toxicity (associated with EGFR inhibition)Gastrointestinal perforation (associated with VEGFR2 inhibition)
06

Interacting drugs

6 more in the full profile.

07

Biomarkers

HER2 overexpression (IHC 3+ or FISH+)EGFR overexpressionClaudin 18.2 expression levelsEpCAM positivity

Beyond the preview

Go deeper on Esophageal neoplasia-associated cell surface markers.

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 Esophageal neoplasia-associated cell surface markers.

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