Chiang Jung-Ying, Lei Fu-Ju, Chang Huan-Jui, Wei Sung-Tai, Wang Chi-Chung, Huang Yen-Chih, Wang Hwai-Lee, Chuang Chi-Fen, Hu Shu-Yu, Hsieh Chia-Hung
Graduate Institute of Biomedical Sciences, China Medical University, Taichung 404328, Taiwan.
Department of Neurosurgery, China Medical University Hsinchu Hospital, Hsinchu 302056, Taiwan.
Cancers (Basel). 2022 Jun 23;14(13):3089. doi: 10.3390/cancers14133089.
Haloperidol is a routine drug for schizophrenia and palliative care of cancer; it also has antitumor effects in several types of cancer. However, the role of haloperidol in endometrial cancer (EC) development is still unclear. Here, we show that chronic haloperidol treatment in clinically relevant doses induced endometrial hyperplasia in normal mice and promoted tumor growth and malignancy in mice with orthotopic EC. The pharmacokinetic study indicated that haloperidol highly accumulated in the uterus of mice. In vitro studies revealed that haloperidol stimulated the cellular transformation of human endometrial epithelial cells (HECCs) and promoted the proliferation, migration, and invasion of human endometrial carcinoma cells (HECCs) by activating nuclear factor kappa B (NF-κB) and its downstream signaling target, colony-stimulating factor 1 (CSF-1). Gain of function of CSF-1 promotes the cellular transformation of HEECs and the malignant progression of HECCs. Moreover, blockade of CSF-1 inhibited haloperidol-promoted EC progression in vitro and in vivo. A population-based cohort study of EC patients further demonstrated that the use of haloperidol was associated with increased EC-specific mortality. Collectively, these findings indicate that clinical use of haloperidol could potentially be harmful to female patients with EC.
氟哌啶醇是治疗精神分裂症和癌症姑息治疗的常用药物;它在几种类型的癌症中也具有抗肿瘤作用。然而,氟哌啶醇在子宫内膜癌(EC)发生发展中的作用仍不清楚。在此,我们表明,以临床相关剂量长期使用氟哌啶醇可诱导正常小鼠子宫内膜增生,并促进原位EC小鼠的肿瘤生长和恶性程度。药代动力学研究表明,氟哌啶醇在小鼠子宫中高度蓄积。体外研究显示,氟哌啶醇通过激活核因子κB(NF-κB)及其下游信号靶点集落刺激因子1(CSF-1),刺激人子宫内膜上皮细胞(HECCs)的细胞转化,并促进人子宫内膜癌细胞(HECCs)的增殖、迁移和侵袭。CSF-1功能获得促进HEECs的细胞转化和HECCs的恶性进展。此外,阻断CSF-1在体外和体内均抑制氟哌啶醇促进的EC进展。一项基于人群的EC患者队列研究进一步表明,使用氟哌啶醇与EC特异性死亡率增加相关。总体而言,这些发现表明,氟哌啶醇的临床使用可能对患有EC的女性患者有害。