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Tiziana Schioppa

Researcher at University of Brescia

Publications -  40
Citations -  6082

Tiziana Schioppa is an academic researcher from University of Brescia. The author has contributed to research in topics: Chemokine & Cytokine. The author has an hindex of 17, co-authored 32 publications receiving 5184 citations. Previous affiliations of Tiziana Schioppa include Humanitas University & Queen Mary University of London.

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Tumour-associated macrophages are a distinct M2 polarised population promoting tumour progression: Potential targets of anti-cancer therapy

TL;DR: Evidence is presented here supporting the view that TAM represent a unique and distinct M2-skewed myeloid population and are a potential target for anti-cancer therapy.
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Regulation of the chemokine receptor CXCR4 by hypoxia.

TL;DR: It is described that oxygen availability is a determinant parameter in the setting of chemotactic responsiveness to stromal-derived factor 1 (CXCL12), and the Hyp–Hyp-inducible factor 1 α–CXCR4 pathway may regulate trafficking in and out of hypoxic tissue microenvironments.
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Role of tumor-associated macrophages in tumor progression and invasion.

TL;DR: Evidence supporting the view that TAM represent a unique and distinct M2-skewed myeloid population and a potential target of anti-cancer therapy is discussed.
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A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-κB and enhanced IRF-3/STAT1 activation)

TL;DR: In this article, the gene expression profile of TAMs isolated from a murine fibrosarcoma in comparison with peritoneal macrophages (PECs) and myeloid suppressor cells (MSCs), using a cDNA microarray technology, was characterized.
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p50 Nuclear Factor-κB Overexpression in Tumor-Associated Macrophages Inhibits M1 Inflammatory Responses and Antitumor Resistance

TL;DR: It is reported that defective responsiveness of TAM from a murine fibrosarcoma and human ovarian carcinoma to M1 activation signals was associated with a massive nuclear localization of the p50 nuclear factor-kappaB (NF-kappB) inhibitory homodimer.