Pereira Mariana, Vale Nuno
PerMed Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Dr. Plácido da Costa, 4200-450 Porto, Portugal.
CINTESIS@RISE, Faculty of Medicine, University of Porto, Alameda Professor Hernâni Monteiro, 4200-319 Porto, Portugal.
Biomedicines. 2024 Mar 14;12(3):647. doi: 10.3390/biomedicines12030647.
This research explores the therapeutic efficacy of Darunavir (DRV), Rilpivirine (RPV), and Etravirine (ETV) against UM-UC-5 bladder cancer cells, addressing the critical need for innovative treatments in bladder cancer research. Through a comprehensive assessment of their individual and combined effects across diverse time intervals, ETV emerges as the most potent drug, with a lowest IC of 5.9 µM, closely followed by RPV (lowest IC of 9.6 µM), while DRV exhibits the least effectiveness (lowest IC of 25.6 µM). Notably, a significant synergistic effect is evident in the ETV and RPV combination, especially at 48 and 72 h for low concentrations. Synergies are also observed with ETV and DRV, albeit to a lesser extent and primarily at 48 h. Conversely, the DRV and RPV combination yields minimal effects, predominantly additive in nature. In summary, this pre-clinical investigation underscores the promising therapeutic potential of ETV and RPV, both as standalone treatments and in combination, hinting at repurposing opportunities in bladder cancer therapy, which could give a new treatment method for this disease that is faster and without as severe side effects as anticancer drugs. These findings represent a substantial stride in advancing personalized medicine within cancer research and will be further scrutinized in forthcoming studies.
本研究探讨了达芦那韦(DRV)、利匹韦林(RPV)和依曲韦林(ETV)对UM-UC-5膀胱癌细胞的治疗效果,满足了膀胱癌研究中对创新治疗方法的迫切需求。通过对它们在不同时间间隔的单独和联合作用进行全面评估,ETV成为最有效的药物,最低IC为5.9 µM,其次是RPV(最低IC为9.6 µM),而DRV的效果最差(最低IC为25.6 µM)。值得注意的是,ETV和RPV联合使用时具有显著的协同效应,尤其是在低浓度下48小时和72小时时。ETV和DRV联合使用时也观察到协同效应,尽管程度较小,主要在48小时时。相反,DRV和RPV联合使用产生的效果最小,主要是相加作用。总之,这项临床前研究强调了ETV和RPV作为单一治疗药物以及联合使用时的潜在治疗前景,暗示了膀胱癌治疗中的重新利用机会,这可能为该疾病提供一种新的治疗方法,比抗癌药物更快且副作用更小。这些发现代表了癌症研究中推进个性化医疗的重大进展,并将在未来的研究中进一步审视。