Vizcarra-Ramos Sayma, Molina-Pineda Andrea, Gutiérrez-Ortega Abel, Herrera-Rodríguez Sara E, Aguilar-Lemarroy Adriana, Jave-Suárez Luis F, López Zaira, Cano Mario E, Hernández-Gutiérrez Rodolfo
Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C. (CIATEJ), Guadalajara 44270, Mexico.
Centro de Investigación Biomédica de Occidente (CIBO), División de Inmunología, Instituto Mexicano del Seguro Social (IMSS), Guadalajara 44340, Mexico.
Pharmaceutics. 2024 Aug 23;16(9):1109. doi: 10.3390/pharmaceutics16091109.
Prostate cancer is a significant global health problem, being the second most common cancer and the fifth leading cause of death in men worldwide. Standard chemotherapy, though effective, often lacks selectivity for tumor cells, resulting in dose-limiting side effects. To address this, innovative biomedical approaches such as electrochemotherapy and electromagnetic hyperthermia have emerged. Electrochemotherapy improves drug delivery by facilitating electroporation, thereby increasing intracellular concentrations of chemotherapeutic agents. This approach reduces dosages and associated adverse effects. Meanwhile, electromagnetic hyperthermia raises the temperature of tumor cells, enhancing their sensitivity to chemotherapy. While previous research has demonstrated the inhibitory effects of magnetic hyperthermia on prostate cancer cell growth both in vitro and in vivo, and its synergy with chemotherapy has shown enhanced tumor remission, limited studies have focused on electrochemotherapy alone or in combination with hyperthermia in prostate cancer models. This study aims to assess the synergistic effects of electromagnetic hyperthermia, with superparamagnetic iron oxide nanoparticles (SPIONs) and electrochemotherapy, with electroporation and the chemotherapeutic drugs bleomycin and cisplatin, on the prostate cancer-derived cell line DU-145/GFP and prostate-derived cell line RWPE-1. Results indicate enhanced cytotoxicity with both treatments (bleomycin and cisplatin) by adding electroporation, demonstrating a particularly pronounced effect with bleomycin. Combining electroporation with hyperthermia significantly augments cytotoxicity. Moreover, electroporation effectively reduced the time of exposure to electromagnetic hyperthermia while magnifying its cytotoxic effects. Future research in in vivo trials may reveal additional insights into the combined effects of these therapies.
前列腺癌是一个重大的全球健康问题,是全球男性中第二常见的癌症和第五大死因。标准化疗虽然有效,但往往对肿瘤细胞缺乏选择性,导致出现剂量限制副作用。为了解决这个问题,诸如电化学疗法和电磁热疗等创新生物医学方法应运而生。电化学疗法通过促进电穿孔来改善药物递送,从而提高化疗药物的细胞内浓度。这种方法降低了剂量和相关的不良反应。同时,电磁热疗提高肿瘤细胞的温度,增强其对化疗的敏感性。虽然先前的研究已经证明磁热疗在体外和体内对前列腺癌细胞生长具有抑制作用,并且其与化疗的协同作用已显示出增强的肿瘤缓解效果,但在前列腺癌模型中,单独关注电化学疗法或其与热疗联合应用的研究较少。本研究旨在评估电磁热疗(使用超顺磁性氧化铁纳米颗粒(SPIONs))和电化学疗法(使用电穿孔以及化疗药物博来霉素和顺铂)对前列腺癌衍生细胞系DU-145/GFP和前列腺衍生细胞系RWPE-1的协同作用。结果表明,通过添加电穿孔,两种治疗方法(博来霉素和顺铂)的细胞毒性均增强,博来霉素的效果尤为显著。将电穿孔与热疗相结合可显著增强细胞毒性。此外,电穿孔有效缩短了电磁热疗的暴露时间,同时放大了其细胞毒性作用。未来的体内试验研究可能会揭示这些疗法联合作用的更多见解。