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Thies Schroeder

Researcher at University of Mainz

Publications -  54
Citations -  4433

Thies Schroeder is an academic researcher from University of Mainz. The author has contributed to research in topics: Hypoxia (medical) & Cancer. The author has an hindex of 23, co-authored 53 publications receiving 3987 citations. Previous affiliations of Thies Schroeder include Duke University & University of Colorado Denver.

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Targeting lactate-fueled respiration selectively kills hypoxic tumor cells in mice

TL;DR: In this paper, the authors identified monocarboxylate transporter 1 (MCT1) as the prominent path for lactate uptake by a human cervix squamous carcinoma cell line that preferentially utilized lactate for oxidative metabolism.
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Elevated tumor lactate concentrations predict for an increased risk of metastases in head-and-neck cancer.

TL;DR: Elevated tumor lactate concentrations are associated with the subsequent development of nodal or distant metastases in head-and-neck cancer patients and this more aggressive malignant phenotype is probably associated with hypoxia-mediated radioresistance and the upregulation of metastasis-associated genes.
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Pleiotropic effects of HIF-1 blockade on tumor radiosensitivity

TL;DR: It is revealed that HIF-1 plays an important role in determining tumor radioresponsiveness through regulating four distinct processes, including promoting ATP metabolism, proliferation, and p53 activation, which has a radiosensitizing effect on tumors.
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Lactate in Solid Malignant Tumors: Potential Basis of a Metabolic Classification in Clinical Oncology

TL;DR: It is proposed that determination of lactate in primary tumors may serve as a basis for a novel metabolic classification which can lead to an improvement of prognosis and therapy in clinical oncology.
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The genomic analysis of lactic acidosis and acidosis response in human cancers.

TL;DR: Genome-scale gene expression studies are developed to dissect transcriptional responses of primary human mammary epithelial cells to lactic acidosis and hypoxia in vitro and to explore how they are linked to clinical tumor phenotypes in vivo, and the utility of genomic analysis that maps expression-based findings from in vitro experiments to human samples is demonstrated.