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以及布雷哌唑的抗肿瘤作用,布雷哌唑是一种新开发的5-羟色胺-多巴胺活性调节剂,具有改善的安全性。

and anti-tumor effects of brexpiprazole, a newly-developed serotonin-dopamine activity modulator with an improved safety profile.

作者信息

Suzuki Shuhei, Yamamoto Masahiro, Togashi Keita, Sanomachi Tomomi, Sugai Asuka, Seino Shizuka, Yoshioka Takashi, Kitanaka Chifumi, Okada Masashi

机构信息

Department of Molecular Cancer Science, Yamagata University School of Medicine, Yamagata 990-9585, Japan.

Department of Clinical Oncology, Yamagata University School of Medicine, Yamagata 990-9585, Japan.

出版信息

Oncotarget. 2019 May 28;10(37):3547-3558. doi: 10.18632/oncotarget.26949.

Abstract

From the perspective of psycho-oncology, antipsychotics are widely used for patients with cancer. Although some antipsychotic drugs have anti-tumor effects, these antipsychotic drugs are not applicable for cancer patients because of their severe side effects. Brexpiprazole, a novel serotonin-dopamine modulator with an improved side effect profile, was developed as a drug that is structurally and pharmacologically related to aripiprazole, which was reported to have anti-cancer effects. However, it remains unknown whether brexpiprazole has anti-cancer effects. In this study, we examined whether brexpiprazole has anti-tumor effects in cancer cells and cancer stem cells (CSCs) of glioblastoma, pancreatic cancer, and lung cancer. Brexpiprazole suppressed cell growth and induced cell death in the cancer cells and the CSCs, and decreased the CSC properties of the CSCs. Brexpiprazole did not exert any cytotoxic effects on non-cancer cells at the anti-cancer effect-inducing concentration. In the cancer cells and the CSCs, brexpiprazole reduced the expression of survivin, an anti-apoptotic protein, whose reduction sensitizes tumor cells to chemotherapeutic reagents. In the preclinical model in which pancreatic CSCs were subcutaneously implanted into nude mice, brexpiprazole suppressed tumor growth, in addition to reducing the expression of Sox2, a marker for CSCs, and survivin. This suggests that brexpiprazole is a promising antipsychotic drug with anti-tumor effects and an improved safety profile.

摘要

从心理肿瘤学的角度来看,抗精神病药物被广泛应用于癌症患者。尽管一些抗精神病药物具有抗肿瘤作用,但由于其严重的副作用,这些抗精神病药物并不适用于癌症患者。布雷哌唑是一种新型的5-羟色胺-多巴胺调节剂,副作用有所改善,它是作为一种在结构和药理上与阿立哌唑相关的药物而开发的,据报道阿立哌唑具有抗癌作用。然而,布雷哌唑是否具有抗癌作用仍不清楚。在本研究中,我们检测了布雷哌唑对胶质母细胞瘤、胰腺癌和肺癌的癌细胞及癌症干细胞(CSCs)是否具有抗肿瘤作用。布雷哌唑抑制癌细胞和癌症干细胞的细胞生长并诱导细胞死亡,同时降低癌症干细胞的干细胞特性。在诱导抗癌作用的浓度下,布雷哌唑对非癌细胞没有任何细胞毒性作用。在癌细胞和癌症干细胞中,布雷哌唑降低了抗凋亡蛋白survivin的表达,该蛋白表达的降低使肿瘤细胞对化疗药物敏感。在将胰腺癌症干细胞皮下植入裸鼠的临床前模型中,布雷哌唑除了降低癌症干细胞标志物Sox2和survivin的表达外,还抑制了肿瘤生长。这表明布雷哌唑是一种有前景的具有抗肿瘤作用且安全性有所改善的抗精神病药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2f2/6544401/f7f06015f55a/oncotarget-10-3547-g001.jpg

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