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pro vyhledávání: '"Renaud Le Floch"'
Supplementary Methods and Figure Legends from Genetic Disruption of Lactate/H+ Symporters (MCTs) and Their Subunit CD147/BASIGIN Sensitizes Glycolytic Tumor Cells to Phenformin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39fe6ff0046319b2983e0e16f546da6d
https://doi.org/10.1158/0008-5472.22406003
https://doi.org/10.1158/0008-5472.22406003
Figure S6: Phenformin/MCT1 inhibition induces an increase in the ROS content and ROS scavengers do not rescue cell death.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3acd82dc51468fea935c6c229b0d5320
https://doi.org/10.1158/0008-5472.22406006.v1
https://doi.org/10.1158/0008-5472.22406006.v1
Figure S4: Glutamine-dependent and -independent rates of oxygen consumption are increased by BSG/MCTs disruption.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5d15a46a6b124f21cbf494be8e2b82a
https://doi.org/10.1158/0008-5472.22406012.v1
https://doi.org/10.1158/0008-5472.22406012.v1
Figure S2: Disruption of BSG, by zinc finger nucleases, reduces lactic acid transport, inhibits glycolysis and sensitizes U87 cells to the MCT1 inhibitor and phenformin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17f879290e2f6859a504a3a7a93581e8
https://doi.org/10.1158/0008-5472.22406018.v1
https://doi.org/10.1158/0008-5472.22406018.v1
Figure S5: BSG/MCT complex knockout sensitizes cells to phenformin, a mitochondrial complex I inhibitor.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e51550e01f0dd14846655495c5e53a9
https://doi.org/10.1158/0008-5472.22406009
https://doi.org/10.1158/0008-5472.22406009
Figure S1: ZFN-mediated MCT4 and BSG gene knockout.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5a66481eed1334cd7490c1dcdafcc89
https://doi.org/10.1158/0008-5472.22406021.v1
https://doi.org/10.1158/0008-5472.22406021.v1
Figure S3: Effect of BSG/MCTs complex disruption on BSG/MCTS mRNA expression and HIF-1 stability.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63e7df92fb23d06e1a62c1ac7b88cbd3
https://doi.org/10.1158/0008-5472.22406015
https://doi.org/10.1158/0008-5472.22406015
Autor:
Ibtissam Marchiq, Renaud Le Floch, Conceição Souto Moura, Sara Granja, Jacques Pouysségur, Fátima Baltazar
Publikováno v:
Scopus-Elsevier
CIÊNCIAVITAE
Oncotarget
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Europe PubMed Central
CIÊNCIAVITAE
Oncotarget
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Europe PubMed Central
Most cancers rely on aerobic glycolysis to generate energy and metabolic intermediates. To maintain a high glycolytic rate, cells must efficiently export lactic acid through the proton-coupled monocarboxylate transporters (MCT1/4). These transporters
Autor:
Moneïm Smani, Marc Landry, Sandrine Arnaud-Dabernat, Pierre-Marie Bourbon, Monique Larou, Karine Massé, Renaud Le Floch, Jean-Yves Daniel, Evelyne Peuchant
Publikováno v:
Experimental Cell Research. 301:293-304
The nm23 gene family encodes nucleoside diphosphate kinases (NDPKs) which supply the cell with (d)NTPs. The human NDPKB, also known as the PuF protein, binds the c-myc promoter and transactivates the c-myc protooncogene. We have now studied the effec
Publikováno v:
Cancer research. 75(1)
Rapidly growing glycolytic tumors require energy and intracellular pH (pHi) homeostasis through the activity of two major monocarboxylate transporters, MCT1 and the hypoxia-inducible MCT4, in intimate association with the glycoprotein CD147/BASIGIN (