4.6 Article

A novel human leiomyoma tissue derived matrix for cell culture studies

期刊

BMC CANCER
卷 15, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12885-015-1944-z

关键词

Tumor microenvironment matrix; Invasion; Migration; Hanging drop; Colony formation; Spheroid formation; Capillary formation

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资金

  1. Science without Borders (CAPES Program) [109/2012, AUXPE-PVES 570/2013]
  2. Sigrid Juselius Foundation
  3. Finnish Cancer Foundation
  4. Finnish Cultural Foundation
  5. Medical Faculty of the University of Oulu
  6. Oulu University Hospital special state support for research and Medical Research Center Oulu

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Background: The composition of the matrix molecules is important in in vitro cell culture experiments of e.g. human cancer invasion and vessel formation. Currently, the mouse Engelbreth-Holm-Swarm (EHS) sarcoma -derived products, such as Matrigel (R), are the most commonly used tumor microenvironment (TME) mimicking matrices for experimental studies. However, since Matrigel (R) is non-human in origin, its molecular composition does not accurately simulate human TME. We have previously described a solid 3D organotypic myoma disc invasion assay, which is derived from human uterus benign leiomyoma tumor. Here, we describe the preparation and analyses of a processed, gelatinous leiomyoma matrix, named Myogel. Methods: A total protein extract, Myogel, was formulated from myoma. The protein contents of Myogel were characterized and its composition and properties compared with a commercial mouse Matrigel (R). Myogel was tested and compared to Matrigel (R) in human cell adhesion, migration, invasion, colony formation, spheroid culture and vessel formation experiments, as well as in a 3D hanging drop video image analysis. Results: We demonstrated that only 34 % of Myogel's molecular content was similar to Matrigel (R). All test results showed that Myogel was comparable with Matrigel (R), and when mixed with low-melting agarose (Myogel-LMA) it was superior to Matrigel (R) in in vitro Transwell (R) invasion and capillary formation assays. Conclusions: In conclusion, we have developed a novel Myogel TME matrix, which is recommended for in vitro human cell culture experiments since it closely mimics the human tumor microenvironment of solid cancers.

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