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dc.rights.licenseopenen_US
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorBASBOUS, Sara
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorPAYSAN, Lisa
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorSENA, Sandra
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorALLAIN, Nathalie
dc.contributor.authorHIRIART, Jean-Baptiste
dc.contributor.authorDUGOT-SENANT, Nathalie
dc.contributor.authorROUSSEAU, Benoît
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorCHEVRET, Edith
ORCID: 0000-0002-9724-8437
IDREF: 08089884X
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorLAGREE, Valerie
ORCID: 0000-0002-5334-4654
IDREF: 248905112
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorMOREAU, Violaine
ORCID: 0000-0002-4513-7022
IDREF: 110852656
dc.date.accessioned2023-01-25T12:37:43Z
dc.date.available2023-01-25T12:37:43Z
dc.date.issued2022-05-01
dc.identifier.issn1476-5500en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/171788
dc.description.abstractEnRnd3/RhoE is an atypical Rho GTPase family member, known to be deregulated in many types of cancer. Previously, we showed that RND3 expression is downregulated in hepatocellular carcinoma (HCC) cell lines and tissues. In cancer cells, Rnd3 is involved in the regulation of cell proliferation and cell invasion. The implication of Rnd3 in HCC invasion was importantly studied whereas its role in cell growth needs further investigation. Thus, in this work, we aimed to better understand the impact of Rnd3 on tumor hepatocyte proliferation. Our results indicate that the silencing of RND3 induces a cell growth arrest both in vitro in 2D and 3D culture conditions and in vivo in tumor xenografts. The growth alteration after RND3 silencing in HCC cells is not due to an increase of cell death but to the induction of senescence. This RND3 knockdown-mediated phenomenon is dependent on the decrease of hTERT expression. Interestingly, after re-expression of RND3, these cells are able to bypass senescence and regain the ability to proliferate, with a re-expression of hTERT. Given that a low expression of Rnd3 is linked to the presence of satellite nodules in HCC, the transient senescence state observed might play a role in cancer progression.
dc.language.isoENen_US
dc.subject.enCarcinoma
dc.subject.enHepatocellular
dc.subject.enCell Line
dc.subject.enTumor
dc.subject.enCell Proliferation
dc.subject.enHumans
dc.subject.enLiver Neoplasms
dc.subject.enrho GTP-Binding Proteins
dc.titleSilencing of RND3/RHOE inhibits the growth of human hepatocellular carcinoma and is associated with reversible senescence
dc.title.alternativeCancer Gene Theren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s41417-022-00445-6en_US
dc.subject.halSciences du Vivant [q-bio]/Cancer
dc.identifier.pubmed35256752en_US
bordeaux.journalCancer Gene Therapyen_US
bordeaux.page437-444en_US
bordeaux.volume29en_US
bordeaux.hal.laboratoriesBRIC (Bordeaux of Institute of Oncology) - U1312en_US
bordeaux.issue5en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03962334
hal.version1
hal.date.transferred2023-01-30T09:38:50Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.title=Silencing%20of%20RND3/RHOE%20inhibits%20the%20growth%20of%20human%20hepatocellular%20carcinoma%20and%20is%20associated%20with%20reversible%20senescence&rft.atitle=Silencing%20of%20RND3/RHOE%20inhibits%20the%20growth%20of%20human%20hepatocellular%20carcinoma%20and%20is%20associated%20with%20reversible%20senescence&rft.jtitle=Cancer%20Gene%20Therapy&rft.date=2022-05-01&rft.volume=29&rft.issue=5&rft.spage=437-444&rft.epage=437-444&rft.eissn=1476-5500&rft.issn=1476-5500&rft.au=BASBOUS,%20Sara&PAYSAN,%20Lisa&SENA,%20Sandra&ALLAIN,%20Nathalie&HIRIART,%20Jean-Baptiste&rft.genre=article


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