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. 2022 Oct 27;12:18051. doi: 10.1038/s41598-022-21706-2

Figure 2.

Figure 2

CMT organoids share important morphological characteristics and hormonal status with their primary tissue. (a) Representative images of H&E stainings of primary tissue (first column), patient-derived organoids (second column), and brightfield images (third column) of 3D organoids of normal mammary epithelium (bottom line) and of mammary tumor (top line) grown in Basement Membrane Extract. The green arrows indicate solid organoids, and the orange ones indicate cystic organoids; the blue arrows indicate luminal secretion. For comparison purposes, two different areas of the same scanned slide are represented for the H&E image of ORG-63-N. Scale bar, 50 μm. (b) Histogram showing the distribution of organoids that are hormone receptor-positive (brown) and negative (grey) grouped per original carcinoma receptor status. (c) Representative images of H&E stainings and immunohistochemical analyses of estrogen receptor (ER), human epidermal growth factor receptor 2 (HER2), Ki67 (marker of cell proliferation), cytokeratin (CK) 5/6 (luminal epithelial cells), and p63 (basal cells) in CMT-63-C tumor and tumor-derived organoids ORG-63-C (passage 3). Scale bar, 50 μm. (d) Representative images of H&E stainings and immunohistochemical analyses of estrogen receptor (ER), human epidermal growth factor receptor 2 (HER2), Ki67 (marker of cell proliferation), cytokeratin (CK) 5/6 (luminal epithelial cells), and p63 (basal cells) in normal mammary epithelium (T-63-N) and tissue-derived organoids ORG-63-N (passage 3). Scale bar, 50 μm.