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Marcelo Boareto

Researcher at ETH Zurich

Publications -  32
Citations -  2099

Marcelo Boareto is an academic researcher from ETH Zurich. The author has contributed to research in topics: Notch signaling pathway & Neural stem cell. The author has an hindex of 14, co-authored 30 publications receiving 1672 citations. Previous affiliations of Marcelo Boareto include University of São Paulo & Swiss Institute of Bioinformatics.

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Implications of the Hybrid Epithelial/Mesenchymal Phenotype in Metastasis

TL;DR: The operating principles of the core regulatory network for EMT/MET that acts as a “three-way” switch giving rise to three distinct phenotypes – E, M and hybrid E/M are reviewed and a theoretical framework that can elucidate the role of many other players in regulating epithelial plasticity is presented.
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Toward understanding cancer stem cell heterogeneity in the tumor microenvironment.

TL;DR: A mechanism-based dynamical model is shown that the diffusion of EMT-inducing signals such as TGF-β, together with noncell autonomous control of E MT and CSC decision making via the Notch signaling pathway, can explain experimentally observed disparate localization of subsets of CSCs with varying EMT phenotypes in the tumor.
Posted Content

Implications of the hybrid epithelial/mesenchymal phenotype in metastasis

TL;DR: In this article, the operating principles of the core regulatory network for EMT/MET are reviewed, which acts as a three-way switch giving rise to three distinct phenotypes - epithelial, mesenchymal and hybrid epithelial/mesenchymals.
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Coupling the modules of EMT and stemness: A tunable ‘stemness window’ model

TL;DR: The results unify various apparently contradictory experimental findings regarding the interconnection between EMT and stemness, corroborate the emerging notion that partial EMT associates with stemhood, and offer new testable predictions.
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Jagged-Delta asymmetry in Notch signaling can give rise to a Sender/Receiver hybrid phenotype.

TL;DR: It is found that the asymmetry between the modulations of Delta and Jagged leads to the existence of the previously unexplored possibility of a Sender–Receiver phenotype enabling two interacting cells to share a similar fate.