The Anti-Nectin 4: A Promising Tumor Cells Target. A Systematic Review

生物标志物 癌症 肿瘤细胞 疾病 计算生物学 细胞 癌症研究 循环肿瘤细胞 医学 临床试验 临床意义 癌细胞 肿瘤进展 评论文章 生物信息学 膀胱癌 生物标志物发现 靶向治疗 实体瘤 人类疾病 肿瘤异质性 肿瘤微环境 细胞粘附 肿瘤科 蛋白质表达
作者
Wafa Bouleftour,Aline Guillot,Nicolas Magne
出处
期刊:Molecular Cancer Therapeutics [American Association for Cancer Research]
卷期号:21 (4): 493-501 被引量:66
标识
DOI:10.1158/1535-7163.mct-21-0846
摘要

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.
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