Yang Danlu, Xu Xingxing, Wang Xin, Feng Wenjin, Shen Xiya, Zhang Jingjing, Liu Huitao, Xie Changnan, Wu Qian, Miao Xuemeng, Guo Yifan, Cai Hao, Wu Lihao, Zhou Shuxian, Yao Xinfei, Wang Ying, Xie Tian, Huang Zhihui
Key Laboratory of β-elemene Anti-cancer Medicine of Zhejiang Province and Holistic Integrative Pharmacy Institutes, and Department of Neurosurgery, The Affiliated Hospital, Hangzhou Normal University Hangzhou 311121, Zhejiang, China.
School of Basic Medical Sciences, Wenzhou Medical University Wenzhou 325035, Zhejiang, China.
Am J Cancer Res. 2021 Feb 1;11(2):370-388. eCollection 2021.
Glioma is currently the most widespread and malignant primary intracranial tumor, which is characterized by high heterogeneity and high fatality rates. β-elemene, which is a bioactive compound extracted from a Chinese herb, Curcuma wenyujin, has been reported to reduce resistance of chemotherapeutic drugs and induce apoptosis in tumor cells. However, the role and mechanisms of β-elemene in glioma senescence remains unknown. In the present study, we found that a low concentration of β-elemene (10 μg/mL) induced senescence in glioma cells, including reduction of cell proliferation, hypertrophic morphology, increase of senescence-associated β-galactosidase (SA-β-Gal) activity, upregulation of several senescence-associated genes such as and , and downregulation of . However, a high concentration of β-elemene induced apoptosis in glioma cells. Treatment with β-elemene caused a marked down-regulation of Yes-associated protein (YAP) expression in glioma cells, which is a key transcriptional co-activator in multiple cancers. Moreover, cyclin dependent kinase 6 (CDK6), which is a known downstream target of YAP, was decreased in glioma cells that treated with β-elemene. The overexpression of YAP and CDK6 significantly rescued β-elemene-induced senescence in glioma cells. Finally, β-elemene treatment also induced the senescence of glioma cells in glioma xenograft model through inactivation of YAP-CDK6 pathways, which might inhibit the glioma growth. Taken together, these results reveal a previously unknown role of β-elemene in glioma cell senescence and that is associated with YAP-CDK6 signaling pathway, which will enhance our understanding of glioma cell senescence, and provide novel strategies for the treatment of gliomas.
胶质瘤是目前最常见且恶性程度最高的原发性颅内肿瘤,具有高度异质性和高死亡率的特点。β-榄香烯是从中药莪术中提取的一种生物活性化合物,据报道它能降低肿瘤细胞对化疗药物的耐药性并诱导其凋亡。然而,β-榄香烯在胶质瘤细胞衰老中的作用及机制尚不清楚。在本研究中,我们发现低浓度的β-榄香烯(10μg/mL)可诱导胶质瘤细胞衰老,包括细胞增殖减少、形态肥大、衰老相关β-半乳糖苷酶(SA-β-Gal)活性增加、若干衰老相关基因如 和 的上调以及 的下调。然而,高浓度的β-榄香烯可诱导胶质瘤细胞凋亡。β-榄香烯处理导致胶质瘤细胞中Yes相关蛋白(YAP)表达显著下调,YAP是多种癌症中的关键转录共激活因子。此外,细胞周期蛋白依赖性激酶6(CDK6)作为YAP已知的下游靶点,在用β-榄香烯处理的胶质瘤细胞中表达降低。YAP和CDK6的过表达显著挽救了β-榄香烯诱导的胶质瘤细胞衰老。最后,β-榄香烯处理还通过YAP-CDK6信号通路失活诱导了胶质瘤异种移植模型中胶质瘤细胞的衰老,这可能抑制胶质瘤生长。综上所述,这些结果揭示了β-榄香烯在胶质瘤细胞衰老中以前未知的作用,且与YAP-CDK6信号通路相关,这将加深我们对胶质瘤细胞衰老的理解,并为胶质瘤的治疗提供新策略。