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A new cell-laden 3D Alginate-Matrigel hydrogel resembles human breast cancer cell malignant morphology, spread and invasion capability observed "in vivo". | LitMetric

AI Article Synopsis

  • - The study aimed to create a 3D material using composite gels of Alginate and Matrigel as a substrate for culturing aggressive breast cancer cells (MDA-MB-231), achieving both structural stability and biological activity.
  • - The researchers focused on how the cells' shape and behavior, particularly the development of invadopodia, related to their malignancy and invasiveness through a novel bioreactor-based assay.
  • - A specific gel composition (50% Alginate, 50% Matrigel) showed significant findings, including unique cell shapes, increased migration through the gel, and potential attachment to vascular-like membranes, indicating a new model for studying metastasis.

Article Abstract

Purpose of this study was the development of a 3D material to be used as substrate for breast cancer cell culture. We developed composite gels constituted by different concentrations of Alginate (A) and Matrigel (M) to obtain a structurally stable-in-time and biologically active substrate. Human aggressive breast cancer cells (i.e. MDA-MB-231) were cultured within the gels. Known the link between cell morphology and malignancy, cells were morphologically characterized and their invasiveness correlated through an innovative bioreactor-based invasion assay. A particular type of gel (i.e. 50% Alginate, 50% Matrigel) emerged thanks to a series of significant results: 1. cells exhibited peculiar cytoskeleton shapes and nuclear fragmentation characteristic of their malignancy; 2. cells expressed the formation of the so-called invadopodia, actin-based protrusion of the plasma membrane through which cells anchor to the extracellular matrix; 3. cells were able to migrate through the gels and attach to an engineered membrane mimicking the vascular walls hosted within bioreactor, providing a completely new 3D in vitro model of the very precursor steps of metastasis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871779PMC
http://dx.doi.org/10.1038/s41598-018-23250-4DOI Listing

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