肿瘤微环境
癌症
肺癌
精密医学
类有机物
个性化医疗
计算生物学
转录组
癌细胞
癌症研究
体内
癌症医学
生物
医学
生物信息学
病理
内科学
神经科学
生物技术
遗传学
基因表达
基因
作者
Yanmei Zhang,Qifan Hu,Yuquan Pei,Hao Luo,Zixuan Wang,Xinxin Xu,Qing Zhang,Jianli Dai,Qianqian Wang,Zilian Fan,Yongcong Fang,Min Ye,Binhan Li,Mailin Chen,Qi Xue,Qingfeng Zheng,Shulin Zhang,Miao Huang,Ting Zhang,Jin Gu
标识
DOI:10.1038/s41467-024-47737-z
摘要
Cancer models play critical roles in basic cancer research and precision medicine. However, current in vitro cancer models are limited by their inability to mimic the three-dimensional architecture and heterogeneous tumor microenvironments (TME) of in vivo tumors. Here, we develop an innovative patient-specific lung cancer assembloid (LCA) model by using droplet microfluidic technology based on a microinjection strategy. This method enables precise manipulation of clinical microsamples and rapid generation of LCAs with good intra-batch consistency in size and cell composition by evenly encapsulating patient tumor-derived TME cells and lung cancer organoids inside microgels. LCAs recapitulate the inter- and intratumoral heterogeneity, TME cellular diversity, and genomic and transcriptomic landscape of their parental tumors. LCA model could reconstruct the functional heterogeneity of cancer-associated fibroblasts and reflect the influence of TME on drug responses compared to cancer organoids. Notably, LCAs accurately replicate the clinical outcomes of patients, suggesting the potential of the LCA model to predict personalized treatments. Collectively, our studies provide a valuable method for precisely fabricating cancer assembloids and a promising LCA model for cancer research and personalized medicine.
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