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Martin Kery

Researcher at Slovak Academy of Sciences

Publications -  8
Citations -  148

Martin Kery is an academic researcher from Slovak Academy of Sciences. The author has contributed to research in topics: Tumor hypoxia & Pyruvate dehydrogenase kinase. The author has an hindex of 5, co-authored 8 publications receiving 93 citations. Previous affiliations of Martin Kery include Ohio State University & The Ohio State University Wexner Medical Center.

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Microenvironmental control of glucose metabolism in tumors by regulation of pyruvate dehydrogenase

TL;DR: A better understanding of PDC's enzymatic regulation in vivo and of the mechanisms of PDHK‐mediated malignant progression is necessary for the design of better PDHK inhibitors and the selection of patients most likely to benefit from such inhibitors.
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CAIX Regulates Invadopodia Formation through Both a pH-Dependent Mechanism and Interplay with Actin Regulatory Proteins.

TL;DR: In vivo localization of CAIX is demonstrated within invadopodia and gives rationale for its targeting during anti-metastatic therapy and confirms the key role of CAix in the metastatic process.
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Lactate stimulates CA IX expression in normoxic cancer cells

TL;DR: By inducing CA IX, lactate can facilitate the maintenance of cancer cell aggressive behavior in normoxia and participation of both HIF-1 and specificity protein 1 (SP1) transcription factors is crucial for lactate-driven normoxic induction of the CA9 gene.
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CA IX Stabilizes Intracellular pH to Maintain Metabolic Reprogramming and Proliferation in Hypoxia.

TL;DR: Results indicate that in the absence of CA IX, reduction of pHi disrupts LDHA activity and hinders the cellular capacity to regenerate NAD+ and secrete protons to the extracellular space, andHypoxia-induced CA IX mediates adaptation to microenvironmental hypoxia and acidosis directly and indirectly by maintaining glycolysis-permissive intracellular milieu.
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Emerging strategies to target cancer metabolism and improve radiation therapy outcomes

TL;DR: There are opportunities to enhance the efficacy of radiotherapy by exploiting cell-inherent vulnerabilities and dynamic microenvironmental components of the tumor by exploiting metabolic pathways in the context of ionizing radiation responses.