Chen Yang, Gao Yun, Yi Xiaojiao, Zhang Jinghui, Chen Zhongjian, Wu Yongjiang
College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.
Institute of Cancer and Basic Medicine (ICBM), Chinese Academy of Sciences, Hangzhou, China.
Front Pharmacol. 2020 Oct 22;11:544647. doi: 10.3389/fphar.2020.544647. eCollection 2020.
Colorectal cancer is a common malignancy occurring in the digestive system, which is the third common cause of cancer mortality in developed countries. Shikonin, a naphthoquinone compound extracted from the root of , is extensively reported to exert antitumor activity against various types of cancer. However, the systematic effect of shikonin in colon cancer remains poorly understood. In the present study, we evaluated the antitumor activity of shikonin in human colon cancer cells and the therapeutic effect on a xenograft mouse model. Transcriptomics and metabolomics were further integrated to provide a systematic perspective of the shikonin-induced antitumor mechanism. The results demonstrated that shikonin had a remarkable antitumor potency both and . Moreover, metabolic pathways, including the purine metabolism, amino acid metabolism, and glycerophospholipid metabolism, were perturbed and subsequently led to cell cycle arrest in the G2/M phase. In particular, the disturbance of purine metabolism may account for the major mechanism resulting from shikonin antitumor activity.
结直肠癌是消化系统常见的恶性肿瘤,在发达国家是癌症死亡的第三大常见原因。紫草素是从紫草根部提取的一种萘醌化合物,广泛报道其对多种类型的癌症具有抗肿瘤活性。然而,紫草素在结肠癌中的系统作用仍知之甚少。在本研究中,我们评估了紫草素在人结肠癌细胞中的抗肿瘤活性以及对异种移植小鼠模型的治疗效果。进一步整合转录组学和代谢组学,以提供紫草素诱导的抗肿瘤机制的系统观点。结果表明,紫草素在体外和体内均具有显著的抗肿瘤效力。此外,包括嘌呤代谢、氨基酸代谢和甘油磷脂代谢在内 的代谢途径受到干扰,随后导致细胞周期停滞在G2/M期。特别是,嘌呤代谢的紊乱可能是紫草素抗肿瘤活性的主要机制。