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Synergistic Anticancer Effects of Cisplatin Combined with Combretastatin A4 Phosphate on Human Osteosarcoma-Xenografted Mice.
Dai, Guo; Zheng, Di; Liu, Gaiwei; Song, Qi.
Afiliación
  • Dai G; Department of Spine Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Zheng D; Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.
  • Liu G; Department of Orthopedics, Jingzhou Central Hospital, Jingzhou, China.
  • Song Q; Department of Trauma Surgery, Wuhan No. 1 Hospital, Wuhan, China.
Cells Tissues Organs ; 210(4): 293-300, 2021.
Article en En | MEDLINE | ID: mdl-34433168
ABSTRACT
This study aimed to investigate the effectiveness of anticancer therapy combining a cytotoxic chemotherapeutic agent, cisplatin (DDP), and a vascular disruptive drug, combretastatin A4 phosphate (CA4P), in osteosarcoma. First, a human osteosarcoma-xenografted mice model was established. Second, the transplanted tumor models were treated with DDP and CA4P in combination or as monotherapy. Third, the therapeutic effects and the mechanism of the drug combination in the inhibition of transplanted tumors was studied. Finally, the toxic effects of the drugs were observed and recorded. The results showed that DDP combined with CA4P significantly inhibited the growth and lung metastasis of transplanted tumors compared with the monotherapy drug group and vehicle control group. Histopathological analysis revealed that apoptotic and necrotic cell death significantly increased in the combination group, and combined treatment significantly inhibited the proliferation of osteosarcoma cells compared with either agent alone or the vehicle control. Additionally, no obvious toxic effects were observed in the combination group. These results indicate that the combined effects of DDP and CA4P on the progression of human osteosarcoma in vivo were superior to that of either agent alone. DDP combined with CA4P exerted synergistic effects at lower concentrations and promoted apoptosis and necrosis, as well as inhibited proliferation of osteosarcoma cells, but it did not increase the systemic toxic effects of chemotherapy. Our findings highlight CA4P as an effective anticancer agent candidate for combination with DDP in clinical applications to treat osteosarcoma.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estilbenos / Neoplasias Óseas / Osteosarcoma Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Cells Tissues Organs Asunto de la revista: ANATOMIA Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estilbenos / Neoplasias Óseas / Osteosarcoma Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Cells Tissues Organs Asunto de la revista: ANATOMIA Año: 2021 Tipo del documento: Article País de afiliación: China