Skip to main content
. 2018 Jun 21;8:9427. doi: 10.1038/s41598-018-27409-x

Figure 1.

Figure 1

In vitro epithelial-to-mesenchymal transition (EMT) induced by Matrigel culture in inflammatory breast cancer. (A) Western blots for E-cadherin, vimentin, and β-actin (a loading control) in a panel of breast cancer cells. ER+, estrogen receptor-positive; TNBC, triple-negative breast cancer; IBC, inflammatory breast cancer. SUM149 is an IBC cell line with triple-negative characteristics. Full-length blots with different exposure times are presented in Supplementary Figures S1 and S2. (B) Bright-field images depicting typical morphologies of breast cancer cells cultured in monolayer or Matrigel culture conditions. The left 2 columns and the right column are the images captured by objective lens with 10X and 4X magnifications, respectively. (C) Transcriptional profiling of EMT markers in IBC cells cultured in monolayer or Matrigel culture conditions, assayed by quantitative RT-PCR. For each marker, the samples from monolayer culture conditions were set as normalizers, and all relative expression values were log2 transformed. Bars, standard error of the mean. (D) Immunofluorescent images depicting expression of E-cadherin (green) and vimentin (red) in SUM149 cells cultured in monolayer or Matrigel culture conditions. Merged images are derived from the images of E-cadherin, vimentin, as well as nuclear counterstaining Hoechst 33342 (blue). Bar, 200 µm.