Cui Hongwei, Han Wenyan, Zhang Junyao, Zhang Zhihui, Su Xiulan
Clinical Medical Research Center of the Affiliated Hospital, Inner Mongolia Medical University, Hohhot, 010050, Inner Mongolia, P.R. China.
J Cancer. 2019 May 26;10(11):2425-2433. doi: 10.7150/jca.31359. eCollection 2019.
Changes in cell metabolism are an important feature of tumors that has always been an intense topic of study, particularly in regard to whether metabolic disorders are a cause or an effect of tumorigenesis. Studies have shown that the processes underlying metabolic changes in tumors involve the activation of protooncogenes and the inactivation of cancer suppressor genes, as well as changes in metabolic flux in cells due to the abnormal activation of signaling pathways that modulate metabolic enzymes and/or metabolic regulatory proteins at several levels, including transfer and posttranslational modification. Thus, the repair of abnormal metabolic pathways via intervention in the relevant tumor metabolic pathways that impact specific targets has become a new method of cancer prevention and treatment. Bioactive peptides, which have many biological functions, could specifically target malignant tumors. Their interaction with signal transduction molecules involved in the development and transference of tumors could regulate the relevant cell metabolic pathways and inhibit the development of tumors and/or accelerate apoptosis in tumor cells. In this review, several aspects of tumor suppression using bioactive peptides will be discussed and summarized, including the regulation of the PI3K/AKT/mTOR, AMPK, and STST3 signaling pathways, the modulation of the TRAIL death receptor signaling pathway, the regulation of aerobic glycolysis by PKM2, and the modulation of the NF-кB signaling pathway, to aid in the search for better and more specific antineoplastic drugs in the form of bioactive peptides.
细胞代谢变化是肿瘤的一个重要特征,一直是研究的热点话题,尤其是关于代谢紊乱是肿瘤发生的原因还是结果。研究表明,肿瘤代谢变化的潜在过程涉及原癌基因的激活和抑癌基因的失活,以及由于信号通路异常激活导致的细胞代谢通量变化,这些信号通路在多个水平上调节代谢酶和/或代谢调节蛋白,包括转移和翻译后修饰。因此,通过干预影响特定靶点的相关肿瘤代谢途径来修复异常代谢途径,已成为癌症预防和治疗的新方法。具有多种生物学功能的生物活性肽可以特异性地靶向恶性肿瘤。它们与参与肿瘤发生和转移的信号转导分子的相互作用可以调节相关的细胞代谢途径,抑制肿瘤的发展和/或加速肿瘤细胞的凋亡。在这篇综述中,将讨论和总结使用生物活性肽抑制肿瘤的几个方面,包括PI3K/AKT/mTOR、AMPK和STST3信号通路的调节;TRAIL死亡受体信号通路的调节;PKM2对有氧糖酵解的调节;以及NF-кB信号通路的调节,以帮助寻找更好、更特异的生物活性肽形式的抗肿瘤药物。