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应对肺癌治疗中耐药性的复杂性:机制、类器官模型及克服治疗失败的策略

Navigating the Complexity of Resistance in Lung Cancer Therapy: Mechanisms, Organoid Models, and Strategies for Overcoming Treatment Failure.

作者信息

Kang Da Hyun, Lee Jisoo, Im Subin, Chung Chaeuk

机构信息

Division of Pulmonology and Critical Care Medicine, Department of Internal Medicine, College of Medicine, Chungnam National University, Daejeon 34134, Republic of Korea.

College of Medicine, Chungnam National University, Daejeon 35015, Republic of Korea.

出版信息

Cancers (Basel). 2024 Nov 28;16(23):3996. doi: 10.3390/cancers16233996.

Abstract

: The persistence of chemotherapy-resistant and dormant cancer cells remains a critical challenge in the treatment of lung cancer. Objectives: This review focuses on non-small cell lung cancer and small cell lung cancer, examining the complex mechanisms that drive treatment resistance. : This review analyzed current studies on chemotherapy resistance in NSCLC and SCLC, focusing on tumor microenvironment, genetic mutations, cancer cell heterogeneity, and emerging therapies. : Conventional chemotherapy and targeted therapies, such as tyrosine kinase inhibitors, often fail due to factors including the tumor microenvironment, genetic mutations, and cancer cell heterogeneity. Dormant cancer cells, which can remain undetected in a quiescent state for extended periods, pose a significant risk of recurrence upon reactivation. These cells, along with intrinsic resistance mechanisms, greatly complicate treatment efforts. Understanding these pathways is crucial for the development of more effective therapies. Emerging strategies, including combination therapies that target multiple pathways, are under investigation to improve treatment outcomes. Innovative approaches, such as antibody-drug conjugates and targeted protein degradation, offer promising solutions by directly delivering cytotoxic agents to cancer cells or degrading proteins that are essential for cancer survival. The lung cancer organoid model shows substantial promise to advance both research and clinical applications in this field, enhancing the ability to study resistance mechanisms and develop personalized treatments. The integration of current research underscores the need for continuous innovation in treatment modalities. : Personalized strategies that combine novel therapies with an in-depth understanding of tumor biology are essential to overcome the challenges posed by treatment-resistant and dormant cancer cells in lung cancer. A multifaceted approach has the potential to significantly improve patient outcomes.

摘要

化疗耐药和休眠癌细胞的持续存在仍然是肺癌治疗中的一个关键挑战。目的:本综述聚焦于非小细胞肺癌和小细胞肺癌,研究导致治疗耐药的复杂机制。:本综述分析了目前关于非小细胞肺癌和小细胞肺癌化疗耐药的研究,重点关注肿瘤微环境、基因突变、癌细胞异质性及新兴疗法。:传统化疗和靶向疗法,如酪氨酸激酶抑制剂,常常因肿瘤微环境、基因突变和癌细胞异质性等因素而失败。休眠癌细胞可长时间处于静止状态而不被发现,一旦重新激活,复发风险很大。这些细胞连同内在耐药机制,极大地增加了治疗难度。了解这些途径对于开发更有效的疗法至关重要。包括针对多种途径的联合疗法在内的新兴策略正在研究中,以改善治疗效果。创新方法,如抗体药物偶联物和靶向蛋白降解,通过直接将细胞毒性药物递送至癌细胞或降解对癌症存活至关重要的蛋白质,提供了有前景的解决方案。肺癌类器官模型在推进该领域的研究和临床应用方面显示出巨大潜力,增强了研究耐药机制和开发个性化治疗的能力。当前研究的整合强调了治疗模式持续创新的必要性。:将新疗法与对肿瘤生物学的深入理解相结合的个性化策略对于克服肺癌中治疗耐药和休眠癌细胞带来的挑战至关重要。多方面的方法有可能显著改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b515/11640395/8b53a72f50eb/cancers-16-03996-g001.jpg

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