Vella Nathan, Fenech Anthony G, Petroni Magri Vanessa
Department of Clinical Pharmacology and Therapeutics, Faculty of Medicine and Surgery, University of Malta, Msida, Malta.
Front Pharmacol. 2024 Sep 23;15:1438067. doi: 10.3389/fphar.2024.1438067. eCollection 2024.
Lung cancer remains one of the leading causes of cancer-related mortality worldwide, necessitating innovative research methodologies to improve treatment outcomes and develop novel strategies. The advent of three-dimensional (3D) cell cultures has marked a significant advancement in lung cancer research, offering a more physiologically relevant model compared to traditional two-dimensional (2D) cultures. This review elucidates the various types of 3D cell culture models currently used in lung cancer pharmacology, including spheroids, organoids and engineered tissue models, having pivotal roles in enhancing our understanding of lung cancer biology, facilitating drug development, and advancing precision medicine. 3D cell culture systems mimic the complex spatial architecture and microenvironment of lung tumours, providing critical insights into the cellular and molecular mechanisms of tumour progression, metastasis and drug responses. Spheroids, derived from commercialized cell lines, effectively model the tumour microenvironment (TME), including the formation of hypoxic and nutrient gradients, crucial for evaluating the penetration and efficacy of anti-cancer therapeutics. Organoids and tumouroids, derived from primary tissues, recapitulate the heterogeneity of lung cancers and are instrumental in personalized medicine approaches, supporting the simulation of pharmacological responses in a patient-specific context. Moreover, these models have been co-cultured with various cell types and biomimicry extracellular matrix (ECM) components to further recapitulate the heterotypic cell-cell and cell-ECM interactions present within the lung TME. 3D cultures have been significantly contributing to the identification of novel therapeutic targets and the understanding of resistance mechanisms against conventional therapies. Therefore, this review summarizes the latest findings in drug research involving lung cancer 3D models, together with the common laboratory-based assays used to study drug effects. Additionally, the integration of 3D cell cultures into lung cancer drug development workflows and precision medicine is discussed. This integration is pivotal in accelerating the translation of laboratory findings into clinical applications, thereby advancing the landscape of lung cancer treatment. By closely mirroring human lung tumours, these models not only enhance our understanding of the disease but also pave the way for the development of more effective and personalized therapeutic strategies.
肺癌仍然是全球癌症相关死亡的主要原因之一,因此需要创新的研究方法来改善治疗效果并制定新策略。三维(3D)细胞培养的出现标志着肺癌研究取得了重大进展,与传统的二维(2D)培养相比,它提供了一个更具生理相关性的模型。本综述阐明了目前在肺癌药理学中使用的各种3D细胞培养模型,包括球体、类器官和工程组织模型,它们在增强我们对肺癌生物学的理解、促进药物开发和推进精准医学方面发挥着关键作用。3D细胞培养系统模拟了肺肿瘤的复杂空间结构和微环境,为肿瘤进展、转移和药物反应的细胞和分子机制提供了重要见解。源自商业化细胞系的球体有效地模拟了肿瘤微环境(TME),包括缺氧和营养梯度的形成,这对于评估抗癌治疗药物的渗透和疗效至关重要。源自原代组织的类器官和肿瘤类器官概括了肺癌的异质性,在个性化医学方法中发挥着重要作用,支持在患者特定背景下模拟药理反应。此外,这些模型已与各种细胞类型和仿生细胞外基质(ECM)成分共培养,以进一步概括肺TME中存在的异型细胞-细胞和细胞-ECM相互作用。3D培养在识别新的治疗靶点和理解对传统疗法的耐药机制方面做出了重大贡献。因此,本综述总结了涉及肺癌3D模型的药物研究的最新发现,以及用于研究药物作用的常见实验室检测方法。此外,还讨论了将3D细胞培养整合到肺癌药物开发工作流程和精准医学中的问题。这种整合对于加速将实验室研究结果转化为临床应用至关重要,从而推动肺癌治疗的发展。通过紧密模拟人类肺肿瘤,这些模型不仅增强了我们对该疾病的理解,还为开发更有效和个性化的治疗策略铺平了道路。