A decellularized lung extracellular matrix/chondroitin sulfate/gelatin/ chitosan-based 3D culture system shapes breast cancer lung metastasis

被引:4
作者
Wang, Le [1 ]
Yang, Jianye [1 ]
Hu, Xueyan [2 ]
Wang, Shuping [3 ]
Wang, Yanxia [4 ]
Sun, Tongyi [1 ]
Wang, Dan [5 ]
Wang, Wenchi [1 ]
Ma, Hailin [2 ]
Wang, Yingshuai [1 ]
Song, Kedong [2 ]
Li, Wenfang [1 ]
机构
[1] Weifang Med Univ, Sch Life Sci & Technol, Weifang 261053, Peoples R China
[2] Dalian Univ Technol, Dalian R&D Ctr Stem Cell & Tissue Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[3] Univ Jinan, Inst Adv Interdisciplinary Res iAIR, Jinan 250022, Peoples R China
[4] Weifang Med Univ, Sch Rehabil Med, Weifang 261053, Peoples R China
[5] Weifang Med Univ, Sch Fdn Med, Dept Phys Educ, Weifang 261053, Peoples R China
来源
BIOMATERIALS ADVANCES | 2023年 / 152卷
基金
中国国家自然科学基金;
关键词
Breast cancer lung metastasis; 3D engineered model; Decellularized lung nano-matrix; Mechanics; Cell behavior; MATRIX STIFFNESS; CELL; SCAFFOLDS;
D O I
10.1016/j.bioadv.2023.213500
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Distal metastasis of breast cancer is a primary cause of death, and the lung is a common metastatic target of breast cancer. However, the role of the lung niche in promoting breast cancer progression is not well understood. Engineered three-dimensional (3D) in vitro models capable of bridging this knowledge gap can be specifically designed to mimic crucial characteristics of the lung niche in a more physiologically relevant context than conventional two-dimensional systems. In this study, two 3D culture systems were developed to mimic the late stage of breast cancer progression at a lung metastatic site. These 3D models were created based on a novel decellularized lung extracellular matrix/chondroitin sulfate/gelatin/chitosan composite material and on a porcine decellularized lung matrix (PDLM), with the former tailored with comparable properties (stiffness, pore size, biochemical composition, and microstructure) to that of the in vivo lung matrix. The different microstructure and stiffness of the two types of scaffolds yielded diverse presentations of MCF-7 cells in terms of cell distri-bution, cell morphology, and migration. Cells showed better extensions with apparent pseudopods and more homogeneous and reduced migration activity on the composite scaffold compared to those on the PDLM scaffold. Furthermore, alveolar-like structures with superior porous connectivity in the composite scaffold remarkably promoted aggressive cell proliferation and viability. In conclusion, a novel lung matrix-mimetic 3D in vitro breast cancer lung metastasis model was developed to clarify the underlying correlativity between lung ECM and breast cancer cells after lung colonization. A better understanding of the effects of biochemical and biophysical envi-ronments of the lung matrix on cell behaviors can help elucidate the potential mechanisms of breast cancer progression and further improve target discovery of therapeutic strategies.
引用
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页数:16
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