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dc.contributor.authorHaidar, Malak
dc.contributor.authorMetheni, Mehdi
dc.contributor.authorBatteux, Frederic
dc.contributor.authorLangsley, Gordon
dc.date.accessioned2018-11-21T13:13:13Z
dc.date.available2018-11-21T13:13:13Z
dc.date.issued2018-11-14
dc.identifier.citationHaidar M, Metheni M, Batteux F, Langsley G (2018) TGF-b2, catalase activity, H2O2 output and metastatic potential of diverse types of tumour. Available: http://dx.doi.org/10.1101/467191.
dc.identifier.doi10.1101/467191
dc.identifier.doi10.1016/j.freeradbiomed.2019.01.010
dc.identifier.urihttp://hdl.handle.net/10754/629953
dc.description.abstractTheileria annulata is a protozoan parasite that infects and transforms bovine macrophages causing a myeloid-leukaemia-like disease called tropical theileriosis. TGF-b2 is highly expressed in many cancer cells and is significantly increased in Theileria-transformed macrophages, as are levels of Reactive Oxygen Species (ROS), notably H2O2. Here, we describe the interplay between TGF-b2 and ROS in cellular transformation. We show that TGF-b2 drives expression of catalase to reduce the amount of H2O2 produced by T. annulata-transformed bovine macrophages, as well as by human lung (A549) and colon cancer (HT-29) cell lines. Theileria-transformed macrophages attenuated for dissemination express less catalase and produce more H2O2, but regain both virulent migratory and matrigel traversal phenotypes when stimulated with TGF-b2, or catalase that reduce H2O2 output. Increased H2O2 output therefore, underpins the aggressive dissemination phenotype of diverse tumour cell types, but in contrast, too much H2O2 can dampen dissemination.
dc.description.sponsorshipWe thank Arnab Pain for fruitful discussion and input when writing the manuscript. MH was supported by a PhD CNR fellowship from the Lebanese government. GL acknowledges support from ANR grant (11 BSV3 01602), Labex ParaFrap (ANR-11-LABX-0024) and core support from INSERM and the CNRS.
dc.publisherCold Spring Harbor Laboratory
dc.relation.urlhttps://www.biorxiv.org/content/early/2018/11/14/467191
dc.rightsArchived with thanks to bioRxiv
dc.subjectTheileria
dc.subjectTGF-β2
dc.subjectROS
dc.subjectCREB
dc.subjectcatalase
dc.subjecthuman cancer
dc.subjecttumorigenesis
dc.titleTGF-b2, catalase activity, H2O2 output and metastatic potential of diverse types of tumour
dc.typePreprint
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentComputational Bioscience Research Center (CBRC)
dc.contributor.departmentPathogen Genomics Laboratory
dc.eprint.versionPre-print
dc.contributor.institutionLaboratoire de Biologie Cellulaire Comparative des Apicomplexes, Faculté de Médecine, Université Paris Descartes - Sorbonne Paris Cité, France.
dc.contributor.institutionInserm U1016, Cnrs UMR8104, Cochin Institute, Paris, 75014 France.
dc.contributor.institutionLaboratoire de Stress Oxydant, Prolifération Cellulaire et Inflammation, Faculté de Médecine, Université Paris Descartes - Sorbonne Paris Cité, France.
kaust.personHaidar, Malak
refterms.dateFOA2018-11-22T07:26:13Z


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