Transwell permeable supports (24 well, 8 µm pore size, Corning, USA) were used to measure the invasion capability of TNBC cells. After the upper chamber was coated at 37℃ with 200 µl of diluted BD Matrigel™ Basement membrane Matrix (BD, USA) gel solution for 4 h, 800 µl DMEM supplemented with 10% FBS was added to the lower chamber. Then, the upper chamber was seeded with 1 × 104 cells in serum-free medium, and the cells were incubated at 37℃ for 24 h. Subsequently, the cells were fixed in 4% paraformaldehyde and stained with 1% crystal violet, after which cotton swabs were used to gently remove the cells remaining on the upper membrane. We counted stained cells under a microscope and assessed cell invasion from five random fields.
Copyright and License information: The Author(s) ©2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this
article to respond.