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Einfluss von RhoA auf die Invasivität von Mammakarzinomzellen

dc.contributor.advisorGründker, Carsten Prof. Dr.
dc.contributor.authorSchömel, Franziska
dc.date.accessioned2021-05-20T09:05:04Z
dc.date.available2021-06-02T00:50:06Z
dc.date.issued2021-05-20
dc.identifier.urihttp://hdl.handle.net/21.11130/00-1735-0000-0008-582A-7
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-8607
dc.language.isodeude
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc610de
dc.titleEinfluss von RhoA auf die Invasivität von Mammakarzinomzellende
dc.typedoctoralThesisde
dc.title.translatedInfluence of RhoA on Inavasiveness of Breast Cancer Cellsde
dc.contributor.refereeGründker, Carsten Prof. Dr.
dc.date.examination2021-05-26
dc.description.abstractengBreast cancer is the most frequent cancer women suffer from. The most common cause of death is metastasis not the tumor itself, in this stage the disease is no longer curable. This underlines the great significance of examining metastasis to understand it and to find possible therapeutic targets. In the present work it was explored which influence a knockdown of the Rho-GTPase protein RhoA has on non-invasive breast cancer cells MCF-7 and T47D. RhoA is well known for its contribution in stressfiber formation and formation of focal adhesions and therefore a non-motile phaenotype. siRNA-interference was used for the knockdown of RhoA and RT-qPCR and Western Blot to prove the success. With different co-culture assays we observed if the knockdown leads to a change in invasion of the cells. Additionally a proliferation assay was performed and the amount and quality of f-Aktin analysed. We found out that in MCF-7 the invasiveness increased significantly and consistently the amount of F-aktin decreased significantly after RhoA-knockdown. We assume that the reduced stressfiber formation after RhoA-knockdown is responsible for the increase of invasion. In T47D these effects could not be observed. The proliferation was not influenced by RhoA-knockdown. Finally the question is discussed if RhoA is a tumor suppressor or an oncogene and how it possibly switches between these different states.de
dc.contributor.coRefereeJohnsen, Steven Prof. Dr.
dc.subject.engRhoAde
dc.subject.engbreast cancerde
dc.subject.enginvasionde
dc.subject.engMCF-7de
dc.subject.engT47Dde
dc.identifier.urnurn:nbn:de:gbv:7-21.11130/00-1735-0000-0008-582A-7-4
dc.affiliation.instituteMedizinische Fakultätde
dc.subject.gokfullGynäkologie / Geburtshilfe / Perinatologie - Allgemein- und Gesamtdarstellungen (PPN619876050)de
dc.description.embargoed2021-06-02
dc.identifier.ppn1758307080


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