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Claudin-6 作为卵巢癌治疗的潜在靶点:新兴药物综述

英文原题:Claudin-6 as a potential target in the treatment of ovarian cancer: a review of emerging drugs.

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Claudin-6 as a potential target in the treatment of ovarian cancer: a review of emerging drugs.

PubMed 2026/07/26(内容时间) Expert Opin Emerg Drugs Q2 · IF 3.8(JCR 2025)

研究概要

Claudin-6靶向治疗为复发性或铂耐药卵巢癌患者代表了一种有前景的进展。在当前的方法中,ADC由于其效力和可控的安全性特征,似乎最接近广泛的临床适用性。未来的成功将取决于标准化的诊断检测、生物标志物驱动的试验设计以及合理的联合策略,以克服耐药性并最大化持久的临床获益。

研究思路结论见上方概要

Claudins是紧密连接的整合组分,在癌症生物学中正展现出新兴作用。恶性转化过程中claudin表达失调使这些蛋白暴露于肿瘤细胞表面,为靶向治疗创造了机会。Claudin-6是一种癌胚蛋白,在正常成人组织中基本不表达,但在相当一部分卵巢癌中异常表达,使其成为有吸引力的治疗靶点。涵盖领域:本综述总结了在卵巢癌中靶向claudin-6的生物学依据,并评估了当前的治疗策略,包括单克隆抗体、抗体药物偶联物、双特异性T细胞衔接器、CAR-T细胞和CAR-NK细胞。该分析基于在主要生物医学数据库中进行的结构化文献检索,包括MEDLINE(通过PubMed)、EMBASE、Scopus和Web of Science,以及ClinicalTrials.gov上正在进行的研究。

展开英文摘要原文

INTRODUCTION: Claudins are integral components of tight junctions with emerging roles in cancer biology. Dysregulated claudin expression during malignant transformation exposes these proteins on the tumor cell surface, creating opportunities for targeted therapy. Claudin-6, an oncofetal protein largely absent from normal adult tissues, is aberrantly expressed in a significant subset of ovarian cancers, making it an attractive therapeutic target. AREAS COVERED: This review summarizes the biological rationale for targeting claudin-6 in ovarian cancer and evaluates current therapeutic strategies, including monoclonal antibodies, antibody-drug conjugates, bispecific T-cell engagers, CAR-T cells, and CAR-NK cells. The analysis is based on a structured literature search conducted in major biomedical databases, including MEDLINE (via PubMed), EMBASE, Scopus, and Web of Science, as well as ClinicalTrials.gov for ongoing studies. EXPERT OPINION: Claudin-6-targeted therapies represent a promising advancement for patients with recurrent or platinum-resistant ovarian cancer. Among current approaches, ADCs appear closest to broad clinical applicability due to their potency and manageable safety profiles. Future success will depend on standardized diagnostic assays, biomarker-driven trial designs, and rational combination strategies to overcome resistance and maximize durable clinical benefit.

论文信息

作者
Ottum S、Sethi N、Demirkiran C、De Tommasi O、Santin AD
单位
Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.United States
文献类型
综述
期刊
Expert opinion on emerging drugs2026 Jul 26
原文标识
PubMed 42466859 · DOI 10.1080/14728214.2026.2706609