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Ibtissam Marchiq

Researcher at University of Nice Sophia Antipolis

Publications -  16
Citations -  1212

Ibtissam Marchiq is an academic researcher from University of Nice Sophia Antipolis. The author has contributed to research in topics: Basigin & Medicine. The author has an hindex of 9, co-authored 11 publications receiving 985 citations. Previous affiliations of Ibtissam Marchiq include Centre national de la recherche scientifique.

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CD147 subunit of lactate/H+ symporters MCT1 and hypoxia-inducible MCT4 is critical for energetics and growth of glycolytic tumors

TL;DR: Findings highlight that the major protumoral action of CD147/Basigin is to control the energetics of glycolytic tumors via MCT1/MCT4 activity and that blocking lactic acid export provides an efficient anticancer strategy.
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Hypoxia, cancer metabolism and the therapeutic benefit of targeting lactate/H+ symporters

TL;DR: The metabolic pathways generating lactate are reviewed, the rationale for targeting lactic acid transporter complexes for the development of efficient and selective anticancer therapies are discussed, and interest in lactate for cancer development appears recently.
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Genetic Disruption of Lactate/H+ Symporters (MCTs) and Their Subunit CD147/BASIGIN Sensitizes Glycolytic Tumor Cells to Phenformin

TL;DR: It is highlighted that inhibition of the MCT/BSG complexes alone or in combination with phenformin provides an acute anticancer strategy to target highly glycolytic tumors.
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Targeting tumour hypoxia to prevent cancer metastasis. From biology, biosensing and technology to drug development: the METOXIA consortium

TL;DR: A large-scale collaborative EU-financed project 2009–2014 denoted METOXIA has studied all the mentioned aspects of hypoxia with the aim of selecting potential targets for new hypoxIA-specific therapy and develop the first stage of tests for this therapy.
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Na+/H+ antiporter (NHE1) and lactate/H+ symporters (MCTs) in pH homeostasis and cancer metabolism

TL;DR: A fully-coupled mathematical model is used to simulate the relative contribution of the Na(+)/H(+)-exchanger NHE1 and the monocarboxylate transporters in response to lactate production, as it occurs in highly hypoxic and glycolytic tumor cells.