Biopharmaceutical Unit, Centre for Biomedical and Biomaterials Research (CBBR), University of Mauritius, Réduit 80837, Mauritius.
Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit 80837, Mauritius.
Molecules. 2023 Feb 2;28(3):1441. doi: 10.3390/molecules28031441.
Cancer is responsible for lifelong disability and decreased quality of life. Cancer-associated changes in metabolism, in particular carbohydrate, lipid, and protein, offer a new paradigm of metabolic hits. Hence, targeting the latter, as well as related cross-linked signalling pathways, can reverse the malignant phenotype of transformed cells. The systemic toxicity and pharmacokinetic limitations of existing drugs prompt the discovery of multi-targeted and safe compounds from natural products. Mushrooms possess biological activities relevant to disease-fighting and to the prevention of cancer. They have a long-standing tradition of use in ethnomedicine and have been included as an adjunct therapy during and after oncological care. Mushroom-derived compounds have also been reported to target the key signature of cancer cells in in vitro and in vivo studies. The identification of metabolic pathways whose inhibition selectively affects cancer cells appears as an interesting approach to halting cell proliferation. For instance, panepoxydone exerted protective mechanisms against breast cancer initiation and progression by suppressing lactate dehydrogenase A expression levels and reinducing lactate dehydrogenase B expression levels. This further led to the accumulation of pyruvate, the activation of the electron transport chain, and increased levels of reactive oxygen species, which eventually triggered mitochondrial apoptosis in the breast cancer cells. Furthermore, the inhibition of hexokinase 2 by neoalbaconol induced selective cytotoxicity against nasopharyngeal carcinoma cell lines, and these effects were also observed in mouse models. Finally, GL22 inhibited hepatic tumour growth by downregulating the mRNA levels of fatty acid-binding proteins and blocking fatty acid transport and impairing cardiolipin biosynthesis. The present review, therefore, will highlight how the metabolites isolated from mushrooms can target potential biomarkers in metabolic reprogramming.
癌症导致终身残疾和生活质量下降。代谢物的改变,特别是碳水化合物、脂质和蛋白质的改变,为代谢打击提供了新的范例。因此,靶向这些代谢物以及相关的交联信号通路,可以逆转转化细胞的恶性表型。现有药物的全身毒性和药代动力学限制促使人们从天然产物中发现多靶点和安全的化合物。蘑菇具有与疾病抗争和预防癌症相关的生物活性。它们在民族医学中有悠久的应用传统,并已被纳入肿瘤治疗期间和之后的辅助治疗。蘑菇衍生化合物也被报道在体外和体内研究中靶向癌细胞的关键特征。抑制代谢途径,这些代谢途径的抑制选择性地影响癌细胞,似乎是阻止细胞增殖的一种有趣方法。例如,panepoxydone 通过抑制乳酸脱氢酶 A 的表达水平并重新诱导乳酸脱氢酶 B 的表达水平,发挥对乳腺癌发生和进展的保护机制。这进一步导致丙酮酸的积累、电子传递链的激活和活性氧水平的增加,最终导致乳腺癌细胞中线粒体凋亡。此外,neoalbaconol 对己糖激酶 2 的抑制诱导了对鼻咽癌细胞系的选择性细胞毒性,并且在小鼠模型中也观察到了这些效应。最后,GL22 通过下调脂肪酸结合蛋白的 mRNA 水平、阻断脂肪酸转运和损害心磷脂生物合成来抑制肝肿瘤生长。因此,本综述将重点介绍从蘑菇中分离的代谢物如何靶向代谢重编程中的潜在生物标志物。