揭示小细胞肺癌:探索循环肿瘤细胞衍生类器官的未开发资源。

Jesús A Pérez-Cabello, Ana Artero-Castro, Sonia Molina-Pinelo
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引用次数: 0

摘要

小细胞肺癌(SCLC)由于其侵袭性行为和预后不佳,在肿瘤学中仍然是一个挑战。尽管在治疗方面取得了进展,但迫切需要新的策略。液体活检的出现改变了SCLC的管理。这种革命性的非侵入性方法允许对循环肿瘤细胞(ctc)进行分析,提供对肿瘤行为和治疗反应的见解。我们的综述集中在一个开创性的前沿:利用ctc来创建三维(3D)类器官模型。这些模型来源于脱离原发肿瘤或转移部位的ctc,具有巨大的癌症研究革命潜力,特别是在SCLC中。我们探索成功建立ctc衍生类器官的基本条件-一种对个性化医疗具有深远影响的变革性方法。我们的评估涵盖了不同的隔离技术,揭示了它们的优点和局限性。此外,我们揭示了控制ctc培养3D类器官的关键因素,精心模拟肿瘤微环境。这篇综述全面阐述了这些类器官的分子特征,展示了它们在识别治疗靶点和预测反应方面的潜力。从本质上讲,我们的综述融合了分离ctc,建立变革性ctc衍生类器官和表征其分子景观的尖端方法。这代表了在复杂的SCLC管理领域推进个性化医疗的一个有希望的前沿,并对转化研究具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Small cell lung cancer unveiled: Exploring the untapped resource of circulating tumor cells-derived organoids.

Small cell lung cancer (SCLC) remains a challenge in oncology due to its aggressive behavior and dismal prognosis. Despite advances in treatments, novel strategies are urgently needed. Enter liquid biopsy-a game-changer in SCLC management. This revolutionary non-invasive approach allows for the analysis of circulating tumor cells (CTCs), offering insights into tumor behavior and treatment responses. Our review focuses on a groundbreaking frontier: harnessing CTCs to create three-dimensional (3D) organoid models. These models, derived from CTCs that break away from the primary tumor or metastatic locations, hold immense potential for revolutionizing cancer research, especially in SCLC. We explore the essential conditions for successfully establishing CTC-derived organoids-a transformative approach with profound implications for personalized medicine. Our evaluation spans diverse isolation techniques, shedding light on their advantages and limitations. Furthermore, we uncover the critical factors governing the cultivation of 3D organoids from CTCs, meticulously mimicking the tumor microenvironment. This review comprehensively elucidates the molecular characterization of these organoids, showcasing their potential in identifying treatment targets and predicting responses. In essence, our review amalgamates cutting-edge methodologies for isolating CTCs, establishing transformative CTC-derived organoids, and characterizing their molecular landscape. This represents a promising frontier for advancing personalized medicine in the complex realm of SCLC management and holds significant implications for translational research.

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