Ribeiro Eduarda, Araújo Diana, Pereira Mariana, Lopes Bruna, Sousa Patrícia, Sousa Ana Catarina, Coelho André, Rêma Alexandra, Alvites Rui, Faria Fátima, Oliveira Cláudia, Porto Beatriz, Maurício Ana Colette, Amorim Irina, Vale Nuno
OncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, Portugal.
CINTESIS@RISE, Faculty of Medicine, University of Porto, Alameda Professor Hernâni Monteiro, 4200-319 Porto, Portugal.
Biomedicines. 2023 Mar 6;11(3):799. doi: 10.3390/biomedicines11030799.
Gastric cancer (GC) ranked as the fifth most incident cancer in 2020 and the third leading cause of cancer mortality. Surgical prevention and radio/chemotherapy are the main approaches used in GC treatment, and there is an urgent need to explore and discover innovative and effective drugs to better treat this disease. A new strategy arises with the use of repurposed drugs. Drug repurposing coupled with drug combination schemes has been gaining interest in the scientific community. The main objective of this project was to evaluate the therapeutic effects of alternative drugs in GC. For that, three GC cell lines (AGS, MKN28, and MKN45) were used and characterized. Cell viability assays were performed with the reference drug 5-fluororacil (5-FU) and three repurposed drugs: natamycin, nitazoxanide, and benztropine. Nitazoxanide displayed the best results, being active in all GC cells. Further, 5-FU and nitazoxanide in combination were tested in MKN28 GC cells, and the results obtained showed that nitazoxanide alone was the most promising drug for GC therapy. This work demonstrated that the repurposing of drugs as single agents has the ability to decrease GC cell viability in a concentration-dependent manner.
胃癌(GC)在2020年是发病率排名第五的癌症,也是癌症死亡的第三大主要原因。手术预防和放化疗是胃癌治疗的主要方法,迫切需要探索和发现创新且有效的药物来更好地治疗这种疾病。利用重新利用的药物产生了一种新策略。药物重新利用与药物联合方案在科学界越来越受到关注。该项目的主要目标是评估替代药物对胃癌的治疗效果。为此,使用并鉴定了三种胃癌细胞系(AGS、MKN28和MKN45)。用参考药物5-氟尿嘧啶(5-FU)和三种重新利用的药物:匹马霉素、硝唑尼特和苯海索进行细胞活力测定。硝唑尼特显示出最佳结果,在所有胃癌细胞中均有活性。此外,在MKN28胃癌细胞中测试了5-FU和硝唑尼特的联合使用,所得结果表明,单独使用硝唑尼特是最有前景的胃癌治疗药物。这项工作表明,将药物重新用作单一药物有能力以浓度依赖的方式降低胃癌细胞活力。