Journal: STAR Protocols
Article Title: Protocol for serial organoid formation assay using primary colorectal cancer tissues to evaluate cancer stem cell activity
doi: 10.1016/j.xpro.2022.101218
Figure Lengend Snippet: Schematic analysis of the colorectal tumor organoids resulting from serial passaging (A) Brightfield images of secondary organoids depicting size difference over the growth stages. Scale bar = 70 μm. (B) High content imaging can be used to establish organoid counts, size, and shape (form factor: FF) variations for control vs. treated conditions. (C) Secondary organoid counts obtained from the serial passage of primary organoid cultures treated with 3 compounds targeting CSC functions in colorectal tumors (BIX01294, UNC0642: G9a inhibitor. YB-0158: Sam68 modulator). Organoid counts were established based on size exclusion (< 40 μm). n≥4 biological replicates from 3 independent patients; ∗∗: p≤0.0053, ∗∗∗: p≤0.0001). (D) Fluorescence imaging of a colorectal tumor organoid by confocal microscopy. A composite image of proliferative cells (Ki-67; green), adherens junctions (E-Cadherin; red), and nuclei (Hoechst 33342; blue) is presented. Scale bar = 30 μm. (E) Tridimensional reconstruction of CRC patient-derived spheroids and organoids from confocal fluorescence microscopy images using the Imaris 9.5 rendering platform. For each type of multicellular structure, immunostaining of the proliferation marker Ki-67 and intestinal self-renewal marker Bmi1 are presented. Scale bar = 30 μm.
Article Snippet: YB-0158 , MedChemExpress , Cat# HY-136541.
Techniques: Passaging, Imaging, Fluorescence, Confocal Microscopy, Derivative Assay, Microscopy, Immunostaining, Marker