Machine learning reveals mesenchymal breast carcinoma cell adaptation in response to matrix stiffness.

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ID: 268816
2021
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Abstract
Epithelial-mesenchymal transition (EMT) and its reverse process, mesenchymal-epithelial transition (MET), are believed to play key roles in facilitating the metastatic cascade. Metastatic lesions often exhibit a similar epithelial-like state to that of the primary tumour, in particular, by forming carcinoma cell clusters via E-cadherin-mediated junctional complexes. However, the factors enabling mesenchymal-like micrometastatic cells to resume growth and reacquire an epithelial phenotype in the target organ microenvironment remain elusive. In this study, we developed a workflow using image-based cell profiling and machine learning to examine morphological, contextual and molecular states of individual breast carcinoma cells (MDA-MB-231). MDA-MB-231 heterogeneous response to the host organ microenvironment was modelled by substrates with controllable stiffness varying from 0.2kPa (soft tissues) to 64kPa (bone tissues). We identified 3 distinct morphological cell types (morphs) varying from compact round-shaped to flattened irregular-shaped cells with lamellipodia, predominantly populating 2-kPa and >16kPa substrates, respectively. These observations were accompanied by significant changes in E-cadherin and vimentin expression. Furthermore, we demonstrate that the bone-mimicking substrate (64kPa) induced multicellular cluster formation accompanied by E-cadherin cell surface localisation. MDA-MB-231 cells responded to different substrate stiffness by morphological adaptation, changes in proliferation rate and cytoskeleton markers, and cluster formation on bone-mimicking substrate. Our results suggest that the stiffest microenvironment can induce MET.
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rozova2021machineplos Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Rozova, Vlada S;Anwer, Ayad G;Guller, Anna E;Es, Hamidreza Aboulkheyr;Khabir, Zahra;Sokolova, Anastasiya I;Gavrilov, Maxim U;Goldys, Ewa M;Warkiani, Majid Ebrahimi;Thiery, Jean Paul;Zvyagin, Andrei V;
Journal PLoS computational biology
Year 2021
DOI
10.1371/journal.pcbi.1009193
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