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Ivermectin decreases the expression of ALDH1 in ovarian cancer cell lines in combination with chemotherapy

dc.contributor.authorSantos, Cláudia
dc.contributor.authorOliveira, Érica
dc.contributor.authorAlly, Sofia
dc.contributor.authorNunes, Mariana
dc.contributor.authorResende, Albina
dc.contributor.authorRicardo, Sara
dc.date.accessioned2026-01-14T11:52:46Z
dc.date.available2026-01-14T11:52:46Z
dc.date.issued2025-05-27
dc.description.abstractCell Microarray (CMA) technology has been established as an essential tool for advancing cancer studies, allowing for the simultaneous protein analysis of multiple samples [1]. This method facilitates the exploration of various biomarkers associated with diagnosis, prognosis, and therapeutic response, making evaluation processes more efficient and comprehensive [1]. Carboplatin and paclitaxel are commonly used chemotherapy drugs for ovarian cancer treatment. Numerous studies have demonstrated that patients often develop resistance, underscoring the need to discover more effective therapeutic options to improve patient outcomes [2]. In oncology, drug repurposing has shown promising results in achieving this goal. Ivermectin, an antiparasitic drug, has been shown to enhance the efficacy of carboplatin and create a synergistic effect when combined with paclitaxel [3]. Aldehyde Dehydrogenase 1 (ALDH1) is an aldehyde catalyzer that plays a crucial role in drug metabolism. The study of this biomarker could be vital to the understanding of treatment resistance found in advanced ovarian cancer. Using the CMA approach, the aim is to explore the ALDH1 expression pattern in two ovarian cancer cell lines, after in vitro treatment with carboplatin, paclitaxel and ivermectin. Two ovarian cancer cell lines were used: OVCAR8, characterized by resistance to Carboplatin, and OVCAR8 PTX R C, which exhibits resistance to both Carboplatin and Paclitaxel [2]. The cells were exposed to chemotherapeutic agents for 48 hours, administered either alone or in combination with Ivermectin. After the incubation period, the cells were collected, formalin-fixed and embedded in Histogel®. Then the samples were paraffin-embedded and cut into glass slides to perform ALDH1 protein detection using immunocytochemistry. In general, ALDH1 expression was found in the cytoplasm of the cells with a dot pattern. Our results show that in both OVCAR8 and OVCAR8 PTX R C cell lines, the treatment with the combinations of carboplatin/paclitaxel plus Ivermectin, whether in 2D or 3D environments, leads to a notable decrease in ALDH1 expression compared to treatments in monotherapy. High levels of ALDH1 are associated with chemoresistance. The low levels of ALDH1 found in ovarian cancer cells treated with Ivermectin plus carboplatin or paclitaxel reveal a more sensitive profile, which could be a promising alternative for ovarian cancer treatment.eng
dc.description.sponsorshipImmunoT4OC_GI2-CESPU-2023
dc.identifier.citationSantos, C., Oliveira, É., Ally, S., Nunes, M., Resende, A., & Ricardo, S. (2025). Ivermectin decreases the expression of ALDH1 in ovarian cancer cell lines in combination with chemotherapy. IV 1H-TOXRUN INTERNATIONAL CONGRESS 2025 - Scientific Letters - Book of Abstracts, 1 (Sup1). https://doi.org/10.48797/sl.2025.305
dc.identifier.doi10.48797/sl.2025.305
dc.identifier.eissn2795-5117
dc.identifier.urihttp://hdl.handle.net/10400.22/31510
dc.language.isoeng
dc.peerreviewedyes
dc.publisherIUCS-CESPU Publishing
dc.relation2020.04720.BD
dc.relation.hasversionhttps://publicacoes.cespu.pt/index.php/sl/article/view/305
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCell microarray
dc.subjectDrug repurposing
dc.subjectOvarian cancer
dc.subjectChemoresistance
dc.subjectALDH1
dc.titleIvermectin decreases the expression of ALDH1 in ovarian cancer cell lines in combination with chemotherapyeng
dc.typeconference poster
dspace.entity.typePublication
oaire.citation.conferenceDate2025-05
oaire.citation.conferencePlacePorto
oaire.citation.titleIV 1H-TOXRUN INTERNATIONAL CONGRESS 2025 - Scientific Letters - Book of Abstracts
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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