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Valbona Luga

Researcher at University of Toronto

Publications -  10
Citations -  2581

Valbona Luga is an academic researcher from University of Toronto. The author has contributed to research in topics: Wnt signaling pathway & Microvesicles. The author has an hindex of 7, co-authored 8 publications receiving 2326 citations. Previous affiliations of Valbona Luga include Mount Sinai Hospital & Lunenfeld-Tanenbaum Research Institute.

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Journal ArticleDOI

Exosomes Mediate Stromal Mobilization of Autocrine Wnt-PCP Signaling in Breast Cancer Cell Migration

TL;DR: It is reported that fibroblast-secreted exosomes promote breast cancer cell (BCC) protrusive activity and motility via Wnt-planar cell polarity (PCP) signaling and it is demonstrated that exosome-stimulated BCC protrusions display mutually exclusive localization of the core PCP complexes.
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High-throughput mapping of a dynamic signaling network in mammalian cells.

TL;DR: LUMIER (for luminescence-based mammalian interactome mapping), an automated high-throughput technology, is developed and applied to the transforming growth factor–β (TGFβ) pathway and it is shown that Occludin regulates TGFβ type I receptor localization for efficient TGF β-dependent dissolution of tight junctions during epithelial-to-mesenchymal transitions.
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Regulation of Planar Cell Polarity by Smurf Ubiquitin Ligases

TL;DR: It is shown that Smurfs engage in a noncanonical Wnt signaling pathway that targets the core PCP protein Prickle1 for ubiquitin-mediated degradation.
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Loss of the Timp gene family is sufficient for the acquisition of the CAF-like cell state

TL;DR: Generating quadruple TIMP knockout (TIMPless) fibroblasts is generated to unleash metalloproteinase activity within the tumour-stromal compartment and it is shown that complete Timp loss is sufficient for the acquisition of hallmark CAF functions.
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Tumor–Stroma Interaction: Revealing Fibroblast-Secreted Exosomes as Potent Regulators of Wnt-Planar Cell Polarity Signaling in Cancer Metastasis

TL;DR: It is revealed that fibroblasts secrete exosomes that promote breast cancer cell (BCC) protrusive activity, motility, and metastasis by activating autocrine Wnt-PCP signaling in BCCs, and it is shown that Wnt ligands produced by BCCs tether to fibroblast exosome upon trafficking of exosomal ligands within BCCs.