Genetic and Functional Modifications Associated with Ovarian Cancer Cell Aggregation and Limited Culture Conditions

dc.contributor.authorGrieco, Joseph P.en
dc.contributor.authorCompton, Stephanie L. E.en
dc.contributor.authorDavis, Grace N.en
dc.contributor.authorGuinan, Jacken
dc.contributor.authorSchmelz, Eva M.en
dc.date.accessioned2023-10-13T12:36:17Zen
dc.date.available2023-10-13T12:36:17Zen
dc.date.issued2023-10-03en
dc.date.updated2023-10-13T12:07:34Zen
dc.description.abstractThe aggregation of cancer cells provides a survival signal for disseminating cancer cells; however, the underlying molecular mechanisms have yet to be elucidated. Using qPCR gene arrays, this study investigated the changes in cancer-specific genes as well as genes regulating mitochondrial quality control, metabolism, and oxidative stress in response to aggregation and hypoxia in our progressive ovarian cancer models representing slow- and fast-developing ovarian cancer. Aggregation increased the expression of anti-apoptotic, stemness, epithelial-mesenchymal transition (EMT), angiogenic, mitophagic, and reactive oxygen species (ROS) scavenging genes and functions, and decreased proliferation, apoptosis, metabolism, and mitochondrial content genes and functions. The incorporation of stromal vascular cells (SVF) from obese mice into the spheroids increased DNA repair and telomere regulatory genes that may represent a link between obesity and ovarian cancer risk. While glucose had no effect, glutamine was essential for aggregation and supported proliferation of the spheroid. In contrast, low glucose and hypoxic culture conditions delayed adhesion and outgrowth capacity of the spheroids independent of their phenotype, decreased mitochondrial mass and polarity, and induced a shift of mitochondrial dynamics towards mitophagy. However, these conditions did not reduce the appearance of polarized mitochondria at adhesion sites, suggesting that adhesion signals that either reversed mitochondrial fragmentation or induced mitobiogenesis can override the impact of low glucose and oxygen levels. Thus, the plasticity of the spheroids’ phenotype supports viability during dissemination, allows for the adaptation to changing conditions such as oxygen and nutrient availability. This may be critical for the development of an aggressive cancer phenotype and, therefore, could represent druggable targets for clinical interventions.en
dc.description.versionPublished versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationGrieco, J.P.; Compton, S.L.E.; Davis, G.N.; Guinan, J.; Schmelz, E.M. Genetic and Functional Modifications Associated with Ovarian Cancer Cell Aggregation and Limited Culture Conditions. Int. J. Mol. Sci. 2023, 24, 14867.en
dc.identifier.doihttps://doi.org/10.3390/ijms241914867en
dc.identifier.urihttp://hdl.handle.net/10919/116464en
dc.language.isoenen
dc.publisherMDPIen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjectovarian canceren
dc.subjectaggregationen
dc.subjectmitophagyen
dc.subjectmitobiogenesisen
dc.subjecthypoxiaen
dc.subjectglucoseen
dc.subjectmetabolismen
dc.subjectangiogenesisen
dc.titleGenetic and Functional Modifications Associated with Ovarian Cancer Cell Aggregation and Limited Culture Conditionsen
dc.title.serialInternational Journal of Molecular Scienceen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten

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