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免疫治疗时代食管胃交界部及胃癌中HER2耐药机制的探讨

Discussion on the mechanism of HER2 resistance in esophagogastric junction and gastric cancer in the era of immunotherapy.

作者信息

Zhang Yan, Fan Wenxuan, Su Fei, Zhang Xiaoling, Du Yunyi, Li Weiling, Gao Yangjun, Hu Wenqing, Zhao Jun

机构信息

Department of Oncology, Changzhi People's Hospital Affiliated to Changzhi Medical College, Changzhi, Shanxi, China.

Graduate School, Changzhi Medical College, Changzhi, Shanxi, China.

出版信息

Hum Vaccin Immunother. 2025 Dec;21(1):2459458. doi: 10.1080/21645515.2025.2459458. Epub 2025 Jan 28.

Abstract

Human epidermal growth factor receptor 2 (HER2) is a critical biomarker and therapeutic target in gastric/gastroesophageal junction (G/GEJ) cancers, despite the initial success of HER2-targeted therapies, such as trastuzumab, resistance to these drugs has emerged as a major impediment to effective long-term treatment. This review examines the mechanisms of drug resistance in HER2-positive G/GEJ cancer, the primary mechanisms of resistance explored include alterations in the HER2 receptor itself, such as mutations and changes in expression levels, as well as downstream signaling pathways, and interactions with the tumor microenvironment (TME). Furthermore, the review discusses the Novel therapeutic approaches, including the use of antibody-drug conjugates (ADCs) and combination therapies are assessed for their potential to enhance outcomes. By integrating recent research findings and clinical trials, this review aims to provide oncologists and researchers with insights into developing more effective treatments for patients with drug-resistant HER2-positive G/GEJ cancer.

摘要

人表皮生长因子受体2(HER2)是胃/胃食管交界(G/GEJ)癌的关键生物标志物和治疗靶点。尽管以HER2为靶点的疗法(如曲妥珠单抗)取得了初步成功,但对这些药物的耐药性已成为有效长期治疗的主要障碍。本综述探讨了HER2阳性G/GEJ癌的耐药机制,所探讨的主要耐药机制包括HER2受体本身的改变,如突变和表达水平变化,以及下游信号通路,还有与肿瘤微环境(TME)的相互作用。此外,本综述讨论了新的治疗方法,包括评估抗体药物偶联物(ADC)和联合疗法增强治疗效果的潜力。通过整合近期研究结果和临床试验,本综述旨在为肿瘤学家和研究人员提供见解,以开发出针对耐药性HER2阳性G/GEJ癌患者更有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64a9/11776468/063b3bc0426f/KHVI_A_2459458_F0001_OC.jpg

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