Ocoxin oral solution triggers DNA damage and cell death in ovarian cancer

[EN]Ovarian cancer is the most fatal of all the reproductive cancers within the female population, mainly due to its late diagnosis that limits surgery and medical treatment. Classically, ovarian cancer therapy has included conventional chemotherapy, and other therapeutic approaches are now being us...

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Detalles Bibliográficos
Autores: Almaraz-Postigo, Sheila, Sanz, Eduardo, Pandiella Alonso, Atanasio, Díaz Rodríguez, María Elena
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Universidad de Salamanca (USAL)
Repositorio:GREDOS. Repositorio Institucional de la Universidad de Salamanca
OAI Identifier:oai:dnet:gredos______::e419002093c5c620bf64122b82b0289b
Acceso en línea:http://hdl.handle.net/10366/171522
Access Level:acceso abierto
Palabra clave:DNA damage
OOS
Antioxidants
Cell death
Ovarian cancer
Zinc Sulfate
Ascorbic Acid
Xenograft Model Antitumor Assays
Histones
Plant Extracts
Humans
DNA Damage
Vitamin B 6
Cell Line
Antineoplastic Agents
Cell Proliferation
Folic Acid
Cell Death
Vitamin B 12
Pantothenic Acid
Pyridoxine
Ovarian Neoplasms
Animals
Mice
3201.01 Oncología
24 Ciencias de la Vida
ácido pantoténico
daño del ADN
humanos
piridoxina
ratones
línea celular
vitamina B 6
extractos de plantas
ácido fólico
ensayos antitumorales por modelo de xenoinjerto
neoplasias ováricas
histonas
animales
ácido ascórbico
antineoplásicos
vitamina B 12
sulfato de zinc
muerte celular
proliferación celular
Descripción
Sumario:[EN]Ovarian cancer is the most fatal of all the reproductive cancers within the female population, mainly due to its late diagnosis that limits surgery and medical treatment. Classically, ovarian cancer therapy has included conventional chemotherapy, and other therapeutic approaches are now being used to treat these patients, but the outcomes of the disease are still poor. Therefore, new strategies are needed to improve life expectancy and life quality of ovarian cancer patients. Considering that, we investigated the effect of the nutritional supplement Ocoxin Oral Solution (OOS) in ovarian cancer models. OOS contains several nutritional supplements, some of them with demonstrated antitumoral action. In vitro studies showed that OOS inhibited the proliferation of several ovarian cancer cell lines, especially of those representative of the endometrioid subtype, in a time- and dose-dependent manner. A fast cell death induction after OOS treatment was observed, and when the molecular mechanisms leading to this effect were investigated, an activation of the DNA damage checkpoint was detected, as shown by activation (phosphorylation) of CHK1 and CHK2 kinases that was followed by the phosphorylation of the target protein histone H2AX. When tested in animal models of ovarian cancer, OOS reduced tumor growth without any observed secondary effects. Moreover, such reduction in tumor proliferation was caused by the induction of DNA damage as corroborated by the in vivo phosphorylation of CHK2 and Histone H2AX. Finally, OOS potentiated the action of carboplatin or olaparib, the standard of care treatments used in ovarian clinics, opening the possibility of including OOS in combination with those standard of care agents in patients with ovarian cancer.