The janus-faced biology of GPNMB: from tissue homeostasis to cancer pathogenesis

Glycoprotein non-metastatic melanoma protein B (GPNMB) is a transmembrane glycoprotein that differentially regulates tissue homeostasis and disease pathogenesis. In physiological contexts, it maintains melanosome biogenesis, osteogenesis, and neuroprotection through domain-specific interactions. Pathologically, tumors exploit GPNMB's dual mechanisms: membrane-bound isoforms mediate T cell exclusion via DC-HIL/Syndecan-4, while soluble GPNMB(sGPNMB) promote metabolic reprogramming through CD44/NF-κB. Clinically, GPNMB overexpression correlates with poor outcomes, notably demonstrating 40% versus 8% ADC response in high- versus low-expressing TNBC (p < 0.001). Emerging data reveal its crosstalk with HER2/FGFR1 pathways and identify K48-ubiquitination as a therapeutic resistance mechanism. These findings position domain-selective GPNMB targeting as a promising precision oncology strategy.

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Publication Details

Journal
Frontiers in Molecular Biosciences
Published
2025-10-17
DOI
https://doi.org/10.3389/fmolb.2025.1664764
Citations
5
Primary Topic
Peptidase Inhibition and Analysis
Type
article
Field-Weighted Citation Impact
5.23
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article

The janus-faced biology of GPNMB: from tissue homeostasis to cancer pathogenesis

Imad Ibrahim Ali Al-Sultan, Cheng Long, Yuan Ma, Yun Li
5 citations
Frontiers in Molecular Biosciences
Peptidase Inhibition and Analysis
5.23
article

The janus-faced biology of GPNMB: from tissue homeostasis to cancer pathogenesis

Imad Ibrahim Ali Al-Sultan, Cheng Long, Yuan Ma, Yun Li
article en
5 citations

Abstract

Glycoprotein non-metastatic melanoma protein B (GPNMB) is a transmembrane glycoprotein that differentially regulates tissue homeostasis and disease pathogenesis. In physiological contexts, it maintains melanosome biogenesis, osteogenesis, and neuroprotection through domain-specific interactions. Pathologically, tumors exploit GPNMB's dual mechanisms: membrane-bound isoforms mediate T cell exclusion via DC-HIL/Syndecan-4, while soluble GPNMB(sGPNMB) promote metabolic reprogramming through CD44/NF-κB. Clinically, GPNMB overexpression correlates with poor outcomes, notably demonstrating 40% versus 8% ADC response in high- versus low-expressing TNBC (p < 0.001). Emerging data reveal its crosstalk with HER2/FGFR1 pathways and identify K48-ubiquitination as a therapeutic resistance mechanism. These findings position domain-selective GPNMB targeting as a promising precision oncology strategy.

Frontiers in Molecular BiosciencesVol. 12
Management and Science University (MY), Affiliated Hospital of North Sichuan Medical College (CN)
Openalex Percentile: Top 4%
Peptidase Inhibition and Analysis
5.23
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The janus-faced biology of GPNMB: from tissue homeostasis to cancer pathogenesis — Imad Ibrahim Ali Al-Sultan, Cheng Long, et al. · Frontiers in Molecular Biosciences (2025) | TGRS Research Map | TGRS