The Anti-Nectin 4: A Promising Tumor Cells Target. A Systematic Review.
Wafa BouleftourAline GuillotNicolas MagnePublished in: Molecular cancer therapeutics (2022)
The Nectin cell adhesion protein 4 (Nectin-4) is overexpressed in multiple human malignancies. Such aberrant expression is correlated with cancer progression and poor prognostic. Nectin-4 has emerged as a potential biomarker and promising targeted therapy. This review aimed to gather the current state of the literature about Nectin-4 relevance in preclinical tumor models and to summarize its clinical relevance regarding cancer. A systematic assessment of literature articles was performed by searching in PUBMED (MEDLINE) from the database inception to May 2021, following PRISMA guidelines. Preclinical models unanimously demonstrated membrane and cytoplasmic location of the Nectin-4. Furthermore, Nectin-4 was overexpressed whatever the location of the solid tumors. Interestingly, a heterogeneity of Nectin-4 expression has been highlighted in bladder urothelial carcinoma. High serum Nectin-4 level was correlated with treatment efficiency and disease progression. Finally, generated anti-drug-conjugated targeting Nectin-4 induced cell death in multiple tumor cell lines. Nectin-4 emerges as a promising target for anticancer drugs development because of its central role in tumorigenesis, and lymphangiogenesis. Enfortumab vedotin targeting Nectin-4 demonstrated encouraging results and should be extended to other types of solid tumors.
Keyphrases
- cell death
- systematic review
- poor prognosis
- photodynamic therapy
- papillary thyroid
- squamous cell carcinoma
- endothelial cells
- cell proliferation
- binding protein
- emergency department
- small molecule
- oxidative stress
- mesenchymal stem cells
- clinical practice
- high glucose
- single cell
- combination therapy
- adverse drug
- stress induced