Literature DB >> 30311621

Interaction study of cancer cells and fibroblasts on a spatially confined oxygen gradient microfluidic chip to investigate the tumor microenvironment.

Wei Sun1, Yuqing Chen, Yuerong Wang, Pei Luo, Min Zhang, Hongyang Zhang, Ping Hu.   

Abstract

This paper reports a single-layered microfluidic device for studying the interaction of cancer cells and fibroblasts in an oxygen gradient. This gradient can be established from 1.9% to 18.8% using a spatially confined oxygen scavenging chemical reaction. Due to the spatial design of the chip, only cancer cells can sustain low oxygen conditions when co-cultured with fibroblasts in the adjacent channels, simulating the cell-cell interactions of the hypoxic cancer cells and the surrounding fibroblasts in tumor microenvironment in vivo. Moreover, a cell migration assay is performed on the chip for studying the tumor invasion ability. The results show that the migration speed of B16 cells is increased by hypoxia and the co-culture with L929 cells. In addition, we use ELISA to quantify the migration-related cytokines transforming growth factor-β1 (TGF-β1) in the microfluidic system. Our results confirm interaction between cancer cells and fibroblasts. This microfluidic device provides new insight for the investigation of tumor microenvironment and cell interactions.

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Year:  2018        PMID: 30311621     DOI: 10.1039/c8an01216d

Source DB:  PubMed          Journal:  Analyst        ISSN: 0003-2654            Impact factor:   4.616


  2 in total

Review 1.  Tumor-on-a-chip for integrating a 3D tumor microenvironment: chemical and mechanical factors.

Authors:  L Wan; C A Neumann; P R LeDuc
Journal:  Lab Chip       Date:  2020-03-03       Impact factor: 6.799

2.  Metabolic Switching of Tumor Cells under Hypoxic Conditions in a Tumor-on-a-chip Model.

Authors:  Valentina Palacio-Castañeda; Lucas Kooijman; Bastien Venzac; Wouter P R Verdurmen; Séverine Le Gac
Journal:  Micromachines (Basel)       Date:  2020-04-04       Impact factor: 2.891

  2 in total

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