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Maria Letizia Taddei

Researcher at University of Florence

Publications -  80
Citations -  4501

Maria Letizia Taddei is an academic researcher from University of Florence. The author has contributed to research in topics: Cancer cell & Cancer. The author has an hindex of 35, co-authored 72 publications receiving 3678 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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Microenvironment and tumor cell plasticity: An easy way out.

TL;DR: This review is focused on tumor microenvironment as a collection of structural and cellular elements promoting plasticity and adaptive programs and analyzes the role of extracellular matrix stiffness, hypoxia, nutrient deprivation, acidity, as well as different cell populations of tumor micro environment.
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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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Mesenchymal Stem Cells are Recruited and Activated into Carcinoma-Associated Fibroblasts by Prostate Cancer Microenvironment-Derived TGF-β1.

TL;DR: Investigating the signaling molecules which regulate the interplay between MSC, prostate carcinoma (PCa) cells and two important cellular types constituting the tumor‐associated stroma, macrophages and fibroblasts, during their progression toward malignancy indicates a prominent role for TGF‐β1 in MSC mobilization and activation strengthened by the fact that the blockade of TGF-β1 signaling impairs MSC promotion of PCa progression.