Xu Fuyan, Xia Yong, Feng Zhanzhan, Lin Wentao, Xue Qiang, Jiang Jinrui, Yu Xi, Peng Cuiting, Luo Min, Yang Yufei, Wei Yuquan, Yu Luoting
Department of Rehabilitation Medicine, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu 610041, China.
Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University Chengdu 610041, China.
Am J Cancer Res. 2019 Mar 1;9(3):459-478. eCollection 2019.
Triple negative breast cancer (TNBC) patients have a high risk of brain metastases. This deadly disease represents a major challenge for successful treatment, in part because of the poor ability of drugs to penetrate the blood-brain barrier. Antipsychotic drugs show good bioavailability in the brain, and some of them have exhibited anticancer effects in several cancer types. In this study, we investigated the potential of repurposing fluphenazine hydrochloride (Flu) for the treatment of TNBC and the brain metastases. Our data showed that Flu inhibited survival of metastatic TNBC cells. It induced G0/G1 cell cycle arrest and promoted mitochondria-mediated intrinsic apoptosis . Pharmacokinetic studies in BALB/c mice showed a brain/plasma drug concentration ratio of Flu above 25 for at least 24 hours after dosing. Flu moderately suppressed tumor growth in a TNBC subcutaneous xenograft mouse model. Importantly, Flu exhibited good anti-metastatic potential in a mouse brain metastasis model with an inhibition rate of 85%. In addition, Flu showed a strong inhibitory effect on spontaneous lung metastasis. Moreover, Flu didn't cause serious side effects in the mice. Taken together, this study prompts further preclinical and clinical investigation into repurposing Flu for treating metastatic TNBC patients, which urgently need new treatment options.
三阴性乳腺癌(TNBC)患者发生脑转移的风险很高。这种致命疾病是成功治疗的一大挑战,部分原因是药物穿透血脑屏障的能力较差。抗精神病药物在大脑中显示出良好的生物利用度,其中一些药物在几种癌症类型中已表现出抗癌作用。在本研究中,我们研究了将盐酸氟奋乃静(Flu)重新用于治疗TNBC及其脑转移的潜力。我们的数据表明,Flu可抑制转移性TNBC细胞的存活。它诱导G0/G1期细胞周期停滞并促进线粒体介导的内源性凋亡。在BALB/c小鼠中的药代动力学研究表明,给药后至少24小时,Flu的脑/血浆药物浓度比高于25。Flu在TNBC皮下异种移植小鼠模型中适度抑制肿瘤生长。重要的是,Flu在小鼠脑转移模型中表现出良好的抗转移潜力,抑制率为85%。此外,Flu对自发性肺转移显示出强烈的抑制作用。而且,Flu在小鼠中未引起严重的副作用。综上所述,本研究促使进一步对将Flu重新用于治疗转移性TNBC患者进行临床前和临床研究,这些患者迫切需要新的治疗选择。