Department of Genetics, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran 1916893813, Iran.
Farhikhtegan Medical Convergence Sciences Research Center, Farhikhtegan Hospital Tehran Medical Sciences, Islamic Azad University, Tehran 1916893813, Iran.
Int J Mol Sci. 2021 Oct 28;22(21):11669. doi: 10.3390/ijms222111669.
As a multifactorial disease, treatment of cancer depends on understanding unique mechanisms involved in its progression. The cancer stem cells (CSCs) are responsible for tumor stemness and by enhancing colony formation, proliferation as well as metastasis, and these cells can also mediate resistance to therapy. Furthermore, the presence of CSCs leads to cancer recurrence and therefore their complete eradication can have immense therapeutic benefits. The present review focuses on targeting CSCs by natural products in cancer therapy. The growth and colony formation capacities of CSCs have been reported can be attenuated by the dietary agents. These compounds can induce apoptosis in CSCs and reduce tumor migration and invasion via EMT inhibition. A variety of molecular pathways including STAT3, Wnt/β-catenin, Sonic Hedgehog, Gli1 and NF-κB undergo down-regulation by dietary agents in suppressing CSC features. Upon exposure to natural agents, a significant decrease occurs in levels of CSC markers including CD44, CD133, ALDH1, Oct4 and Nanog to impair cancer stemness. Furthermore, CSC suppression by dietary agents can enhance sensitivity of tumors to chemotherapy and radiotherapy. In addition to in vitro studies, as well as experiments on the different preclinical models have shown capacity of natural products in suppressing cancer stemness. Furthermore, use of nanostructures for improving therapeutic impact of dietary agents is recommended to rapidly translate preclinical findings for clinical use.
作为一种多因素疾病,癌症的治疗取决于对其进展中涉及的独特机制的理解。癌症干细胞(CSC)负责肿瘤的干性,并通过增强集落形成、增殖和转移能力,这些细胞还可以介导对治疗的耐药性。此外,CSC 的存在导致癌症复发,因此彻底消除它们可以带来巨大的治疗益处。本综述重点关注天然产物在癌症治疗中靶向 CSC。已经报道,CSC 的生长和集落形成能力可以被膳食因子削弱。这些化合物可以通过诱导 CSC 凋亡和通过 EMT 抑制减少肿瘤迁移和侵袭,从而降低 CSC 的迁移和侵袭能力。多种分子途径,包括 STAT3、Wnt/β-catenin、Sonic Hedgehog、Gli1 和 NF-κB,在抑制 CSC 特征方面,通过膳食因子的下调而发生下调。在天然药物的作用下,CSC 标志物如 CD44、CD133、ALDH1、Oct4 和 Nanog 的水平显著下降,从而损害癌症干性。此外,膳食因子对 CSC 的抑制作用可以提高肿瘤对化疗和放疗的敏感性。除了体外研究和不同的临床前模型实验表明,天然产物具有抑制癌症干性的能力。此外,建议使用纳米结构来提高膳食因子的治疗效果,以便将临床前发现迅速转化为临床应用。