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Tania Fiaschi

Researcher at University of Florence

Publications -  83
Citations -  3637

Tania Fiaschi is an academic researcher from University of Florence. The author has contributed to research in topics: Adiponectin & Acylphosphatase. The author has an hindex of 29, co-authored 78 publications receiving 3179 citations.

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Reciprocal Metabolic Reprogramming through Lactate Shuttle Coordinately Influences Tumor-Stroma Interplay

TL;DR: The reciprocal interplay between CAFs and prostate cancer cells goes beyond the engagement of EMT to include mutual metabolic reprogramming, and cancer cells allocate Warburg metabolism to their corrupted CAFs, exploiting their byproducts to grow in a low glucose environment, symbiotically adapting with stromal cells to glucose availability.
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Anoikis: an emerging hallmark in health and diseases

TL;DR: The aim of this review is to analyse the molecular mechanisms governing both anoikis and anoIKis resistance, focusing on their regulation in physiological processes, as well as in several diseases, including metastatic cancers, cardiovascular diseases and diabetes.
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Oxidative stress, tumor microenvironment, and metabolic reprogramming: a diabolic liaison

TL;DR: The role of oxidant species in the acquisition of two mandatory features for aggressive neoplastic cells, recently defined by Hanahan and Weinberg as new “hallmarks of cancer”: tumor microenvironment and metabolic reprogramming of cancer cells are focused on.
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Two vicinal cysteines confer a peculiar redox regulation to low molecular weight protein tyrosine phosphatase in response to platelet-derived growth factor receptor stimulation.

TL;DR: It is proposed that the presence of an additional Cysteine near the catalytic cysteine could confer to LMW-PTP the ability to rapidly recover its activity and finely regulate PDGF receptor activation during both extracellularly and intracellularly generated oxidative stress.
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Redox Regulation of β-Actin during Integrin-mediated Cell Adhesion

TL;DR: Evidence of in vivo actin redox regulation by a physiological source of reactive oxygen species, specifically those species generated by integrin receptors during cell adhesion, is reported, suggesting that actin glutathionylation is essential for cell spreading and cytoskeleton organization and that it plays a key role in disassembly of actinomyosin complex during cellAdhesion.