Target intelligence / Profile preview

Tripartite motif-containing protein 62 (TRIM62)

Target
TRIM62
Molecular classification
Enzyme (specifically, E3 ubiquitin-protein ligase), Tripartite motif (TRIM) family protein, Zinc finger protein
01

Overview

Tripartite motif-containing protein 62 (TRIM62) is an E3 ubiquitin-protein ligase of the TRIM (tripartite motif) family involved in the regulation of innate immunity, antifungal responses, inflammation, and cancer. It mediates Lys-27–linked ubiquitination of CARD9, activating immune signaling pathways including NF-κB and p38 MAP kinase. Functionally, it also acts as a tumor suppressor in epithelial tissues, influences epithelial polarity, and modulates tissue morphogenesis by regulating SMAD3 and TGF-β–induced epithelial-mesenchymal transition (EMT). Loss or dysregulation of TRIM62 is associated with increased tumorigenesis, disrupted tissue homeostasis, inflammation-induced muscle wasting, and susceptibility to infection. Although not a direct target of approved drugs, TRIM62 is recognized as a key protein in innate immunity, cancer biology, and tissue remodeling.

Other names
E3 ubiquitin-protein ligase TRIM62DEAR1ductal epithelium-associated RING Chromosome 1FLJ10759RING-type E3 ubiquitin transferase TRIM62
02

Mechanism of action

Drugs targeting this molecule would likely act through inhibition or modulation of E3 ubiquitin ligase activity; possibly affect CARD9-mediated signaling, NF-κB activation, or TGF-β/EMT processes, but no approved mechanisms for direct pharmacological targeting of TRIM62

03

Biological functions

Ubiquitin ligase activity (E3)Modulation of innate immune signalingRegulation of NF-κB and MAP kinase (p38) pathwaysPromotion of antifungal responses via CARD9 ubiquitinationTumor suppressor (epithelial morphogenesis, epithelial polarity)Regulation of inflammation and muscle atrophyModulation of TGF-β-induced epithelial-mesenchymal transition (EMT)
04

Disease associations

Cancer (e.g., breast, epithelial, hepatocellular carcinoma, possibly leukemia and cervical cancer)Immunodeficiency (e.g., Immunodeficiency 27B)Muscle atrophy and inflammation (ICU-acquired weakness)Cataract (Multiple Types)Other (roles in infection/inflammation and tissue homeostasis)
05

Safety considerations

Therapeutic targeting may risk disrupting innate immunity, antifungal responses, or normal tissue architecture due to roles in immunity, cell signaling, and tumor suppression
06

Biomarkers

TRIM62 expression (prognostic biomarker for poor clinical outcome in early-onset breast cancer, loss of expression as tumor suppressor marker)TRIM62 levels for muscle inflammation/atrophy risk

Beyond the preview

Go deeper on Tripartite motif-containing protein 62 (TRIM62).

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 Tripartite motif-containing protein 62 (TRIM62).

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