Wu Dinglan, Wang Zhu, Lin Muqi, Shang Yi, Wang Fei, Zhou JiaYi, Wang Fei, Zhang Xiantong, Luo Xiaomin, Huang Weiren
Shenzhen Key Laboratory of Viral Oncology, The Clinical Innovation & Research Centre, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Department of Urology, People's Hospital of Longhua Shenzhen, Southern Medical University, Shenzhen, China.
Front Pharmacol. 2019 Nov 8;10:1287. doi: 10.3389/fphar.2019.01287. eCollection 2019.
Cucurbitacin C (CuC), a novel analogue of triterpenoids cucurbitacins, confers a bitter taste in cucumber. Genes and signaling pathways responsive for biosynthesis of CuC have been identified in the recent years. In the present study, we explored the anti-cancer effects of CuC against human cancers and . CuC inhibited proliferation and clonogenic potential of multiple cancer cells in a dose-dependent manner. Low-dose CuC treatment induced cell cycle arrest at G1 or G2/M stage in different cancer lines, whereas high-dose treatment of CuC caused apoptosis in cancer cells. PI3K-Akt signaling pathway was found to be one of the major pathways involved in CuC-induced cell growth arrest and apoptosis by RNA-Seq and Western blotting. Mechanistic dissection further confirmed that CuC effectively inhibited the Akt signaling by inhibition of Akt phosphorylation at Ser473. CuC treatment (0.1 mg/kg body weight) effectively inhibited growth of cancer cell-derived xenograft tumors in athymic nude mice and caused significant apoptosis. Our findings for the first time demonstrated the potential therapeutic significance of CuC against human cancers.
葫芦素C(CuC)是三萜类葫芦素的一种新型类似物,赋予黄瓜苦味。近年来,已鉴定出与CuC生物合成相关的基因和信号通路。在本研究中,我们探究了CuC对人类癌症的抗癌作用。CuC以剂量依赖的方式抑制多种癌细胞的增殖和克隆形成潜力。低剂量CuC处理在不同癌细胞系中诱导细胞周期停滞于G1或G2/M期,而高剂量CuC处理导致癌细胞凋亡。通过RNA测序和蛋白质免疫印迹发现,PI3K-Akt信号通路是参与CuC诱导的细胞生长停滞和凋亡的主要信号通路之一。机制剖析进一步证实,CuC通过抑制Akt在Ser473位点的磷酸化有效抑制Akt信号传导。CuC处理(0.1mg/kg体重)有效抑制无胸腺裸鼠体内癌细胞衍生的异种移植肿瘤的生长,并导致显著凋亡。我们的研究结果首次证明了CuC对人类癌症的潜在治疗意义。