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3D胶原蛋白-纳米纤维素基质模拟胰腺癌的肿瘤微环境。

3D Collagen-Nanocellulose Matrices Model the Tumour Microenvironment of Pancreatic Cancer.

作者信息

Curvello Rodrigo, Kast Verena, Abuwarwar Mohammed H, Fletcher Anne L, Garnier Gil, Loessner Daniela

机构信息

Department of Chemical Engineering, Faculty of Engineering, Monash University, Clayton, VIC, Australia.

Max Bergmann Center of Biomaterials Dresden, Leibniz Institute of Polymer Research Dresden E.V., Dresden, Germany.

出版信息

Front Digit Health. 2021 Jul 26;3:704584. doi: 10.3389/fdgth.2021.704584. eCollection 2021.

Abstract

Three-dimensional (3D) cancer models are invaluable tools designed to study tumour biology and new treatments. Pancreatic ductal adenocarcinoma (PDAC), one of the deadliest types of cancer, has been progressively explored with bioengineered 3D approaches by deconstructing elements of its tumour microenvironment. Here, we investigated the suitability of collagen-nanocellulose hydrogels to mimic the extracellular matrix of PDAC and to promote the formation of tumour spheroids and multicellular 3D cultures with stromal cells. Blending of type I collagen fibrils and cellulose nanofibres formed a matrix of controllable stiffness, which resembled the lower profile of pancreatic tumour tissues. Collagen-nanocellulose hydrogels supported the growth of tumour spheroids and multicellular 3D cultures, with increased metabolic activity and matrix stiffness. To validate our 3D cancer model, we tested the individual and combined effects of the anti-cancer compound triptolide and the chemotherapeutics gemcitabine and paclitaxel, resulting in differential cell responses. Our blended 3D matrices with tuneable mechanical properties consistently maintain the growth of PDAC cells and its cellular microenvironment and allow the screening of anti-cancer treatments.

摘要

三维(3D)癌症模型是用于研究肿瘤生物学和新治疗方法的宝贵工具。胰腺导管腺癌(PDAC)是最致命的癌症类型之一,通过解构其肿瘤微环境的要素,人们已逐步采用生物工程3D方法对其进行研究。在此,我们研究了胶原蛋白-纳米纤维素水凝胶模拟PDAC细胞外基质以及促进肿瘤球体形成和与基质细胞形成多细胞3D培养物的适用性。I型胶原纤维与纤维素纳米纤维的混合形成了具有可控硬度的基质,类似于胰腺肿瘤组织的较低硬度。胶原蛋白-纳米纤维素水凝胶支持肿瘤球体和多细胞3D培养物的生长,同时增加了代谢活性和基质硬度。为验证我们的3D癌症模型,我们测试了抗癌化合物雷公藤内酯醇与化疗药物吉西他滨和紫杉醇的单独及联合作用,结果产生了不同的细胞反应。我们具有可调机械性能的混合3D基质始终能维持PDAC细胞及其细胞微环境的生长,并允许对抗癌治疗进行筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64b0/8521838/2011a5b72ded/fdgth-03-704584-g0001.jpg

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