High-content microscopy reveals a morphological signature of bortezomib resistance.
Ontology highlight
ABSTRACT: Drug resistance is a challenge in anticancer therapy. In many cases, cancers can be resistant to the drug prior to exposure, that is, possess intrinsic drug resistance. However, we lack target-independent methods to anticipate resistance in cancer cell lines or characterize intrinsic drug resistance without a priori knowledge of its cause. We hypothesized that cell morphology could provide an unbiased readout of drug resistance. To test this hypothesis, we used HCT116 cells, a mismatch repair-deficient cancer cell line, to isolate clones that were resistant or sensitive to bortezomib, a well-characterized proteasome inhibitor and anticancer drug to which many cancer cells possess intrinsic resistance. We then expanded these clones and measured high-dimensional single-cell morphology profil
SUBMITTER: Kelley ME
PROVIDER: S-EPMC10584373 | biostudies-literature | 2023 Sep
REPOSITORIES: biostudies-literature
ACCESS DATA