Chen Vincent Chin-Hung, Hsieh Yi-Hsuan, Lin Tzu-Chin, Lu Mong-Liang, Liao Yin-To, Yang Yao-Hsu, Hsu Tsai-Ching, Stewart Robert, Weng Jun-Cheng, Lee Min-Jing, Chiu Wei-Che, Tzang Bor-Show
Department of Psychiatry, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.
School of Medicine, Chang Gung University, Taoyuan 33302, Taiwan.
Cancers (Basel). 2020 Jun 12;12(6):1560. doi: 10.3390/cancers12061560.
The potential of old drugs in novel indications is being greatly valued. We propose a triple-model study involving population-based, cell, and animal studies to investigate the effects of risperidone, a type of second-generation antipsychotic (SGA) drug, on colorectal cancer. We used data from Taiwan's National Health Insurance Research Database between 1997 and 2013 to compare 101,989 patients with colorectal cancer and 101,989 controls. Conditional logistic regression analyses were used to explore the association between SGA exposure and the risk of colorectal cancer. The following bench studies were performed to evaluate the findings of the population-based study. We found that SGAs had been less commonly used in colorectal cancer patients than in controls. The colorectal cancer risk was reduced with an increase in the cumulative defined daily dose (cDDD) of SGAs. The adjusted odds ratio of antipsychotic use for cDDD days was 0.32 (95% CI: 0.25-0.42). Risperidone exhibited the most prominent tumor inhibition effect in a cell screen study. Bench data revealed that risperidone significantly induced apoptosis and elevated intracellular ROS in human SW480 cells and suppressed the proliferation of the xenografted SW480 tumor in nude mice. Conclusion: This triple-model study demonstrates the association between risperidone usage and a lower risk of colorectal cancer.
老药在新适应症方面的潜力正受到高度重视。我们提出了一项三模型研究,包括基于人群、细胞和动物的研究,以调查第二代抗精神病药物(SGA)利培酮对结直肠癌的影响。我们使用了1997年至2013年台湾国民健康保险研究数据库的数据,比较了101989例结直肠癌患者和101989例对照。采用条件逻辑回归分析来探讨SGA暴露与结直肠癌风险之间的关联。进行了以下基础研究以评估基于人群研究的结果。我们发现,SGA在结直肠癌患者中的使用频率低于对照组。随着SGA累积限定日剂量(cDDD)的增加,结直肠癌风险降低。抗精神病药物使用cDDD天数的调整比值比为0.32(95%CI:0.25 - 0.42)。在细胞筛选研究中,利培酮表现出最显著的肿瘤抑制作用。基础数据显示,利培酮显著诱导人SW480细胞凋亡并升高细胞内ROS水平,并抑制裸鼠体内移植的SW480肿瘤的增殖。结论:这项三模型研究证明了利培酮使用与较低结直肠癌风险之间的关联。