Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/145250
Full metadata record
DC FieldValueLanguage
dc.creatorNunes, M
dc.creatorAbreu, MH
dc.creatorBartosch, C
dc.creatorRicardo, S
dc.date.accessioned2022-11-17T11:32:58Z-
dc.date.available2022-11-17T11:32:58Z-
dc.date.issued2020
dc.identifier.issn1661-6596
dc.identifier.urihttps://hdl.handle.net/10216/145250-
dc.description.abstractThe main challenge in ovarian cancer treatment is the management of recurrences. Facing this scenario, therapy selection is based on multiple factors to define the best treatment sequence. Target therapies, such as bevacizumab and polymerase (PARP) inhibitors, improved patient survival. However, despite their achievements, ovarian cancer survival remains poor; these therapeutic options are highly costly and can be associated with potential side effects. Recently, it has been shown that the combination of repurposed, conventional, chemotherapeutic drugs could be an alternative, presenting good patient outcomes with few side effects and low costs for healthcare institutions. The main aim of this review is to strengthen the importance of repurposed drugs as therapeutic alternatives, and to propose an in vitro model to assess the therapeutic value. Herein, we compiled the current knowledge on the most promising non-oncological drugs for ovarian cancer treatment, focusing on statins, metformin, bisphosphonates, ivermectin, itraconazole, and ritonavir. We discuss the primary drug use, anticancer mechanisms, and applicability in ovarian cancer. Finally, we propose the use of these therapies to perform drug efficacy tests in ovarian cancer ex vivo cultures. This personalized testing approach could be crucial to validate the existing evidences supporting the use of repurposed drugs for ovarian cancer treatment.
dc.description.sponsorshipFunding: This manuscript was funded by HOPE: Improving ovarian cancer patients’ survival—donation from an ovarian cancer patient and by the FCT (Fundação para a Ciência e a Tecnologia) project PTDC/MEC-ONC/29503/2017.
dc.language.isoeng
dc.publisherMDPI
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FMEC-ONC%2F29503%2F2017/PT
dc.relation.ispartofInternational Journal of Molecular Sciences, vol.21(20):7768
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectChemoresistance
dc.subjectDrug repurposing
dc.subjectEx vivo cultures
dc.subjectOvarian cancer
dc.subject.meshDiphosphonates / therapeutic use
dc.subject.meshDrug Repositioning / methods
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshHydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use
dc.subject.meshItraconazole / therapeutic use
dc.subject.meshIvermectin / therapeutic use
dc.subject.meshMetformin / therapeutic use
dc.subject.meshNeoplasm Recurrence, Local / prevention & control
dc.subject.meshOvarian Neoplasms / drug therapy
dc.subject.meshOvarian Neoplasms / pathology
dc.subject.meshRitonavir / therapeutic use
dc.titleRecycling the purpose of old drugs to treat ovarian cancer
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3390/ijms21207768
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/21/20/7768
Appears in Collections:I3S - Artigo em Revista Científica Internacional

Files in This Item:
File Description SizeFormat 
10.3390-ijms21207768.pdf1.19 MBAdobe PDFThumbnail
View/Open


This item is licensed under a Creative Commons License Creative Commons