CEDOC, Chronic Diseases Research Centre, NOVA Medical School | Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.
Instituto Português de Oncologia de Lisboa Francisco Gentil (IPOLFG), Lisbon, Portugal.
Adv Exp Med Biol. 2020;1219:1-34. doi: 10.1007/978-3-030-34025-4_1.
The microenvironment depends and generates dependence on all the cells and structures that share the same niche, the biotope. The contemporaneous view of the tumor microenvironment (TME) agrees with this idea. The cells that make up the tumor, whether malignant or not, behave similarly to classes of elements within a living community. These elements inhabit, modify and benefit from all the facilities the microenvironment has to offer and that will contribute to the survival and growth of the tumor and the progression of the disease.The metabolic adaptation to microenvironment is a crucial process conducting to an established tumor able to grow locally, invade and metastasized. The metastatic cancer cells are reasonable more plastic than non-metastatic cancer cells, because the previous ones must survive in the microenvironment where the primary tumor develops and in addition, they must prosper in the microenvironment in the metastasized organ.The metabolic remodeling requires not only the adjustment of metabolic pathways per se but also the readjustment of signaling pathways that will receive and obey to the extracellular instructions, commanding the metabolic adaptation. Many diverse players are pivotal in cancer metabolic fitness from the initial signaling stimuli, going through the activation or repression of genes, until the phenotype display. The new phenotype will permit the import and consumption of organic compounds, useful for energy and biomass production, and the export of metabolic products that are useless or must be secreted for a further recycling or controlled uptake. In the metabolic network, three subsets of players are pivotal: (1) the organic compounds; (2) the transmembrane transporters, and (3) the enzymes.This chapter will present the "Pharaonic" intent of diagraming the interplay between these three elements in an attempt of simplifying and, at the same time, of showing the complex sight of cancer metabolism, addressing the orchestrating role of microenvironment and highlighting the influence of non-cancerous cells.
肿瘤微环境(TME)的现代观点也同意这一观点。构成肿瘤的细胞,无论是恶性的还是非恶性的,其行为都类似于生物群落中元素的分类。这些元素栖息、修饰并受益于微环境提供的所有设施,这些设施将有助于肿瘤的生存和生长以及疾病的进展。对微环境的代谢适应是一个关键过程,导致能够局部生长、侵袭和转移的已建立的肿瘤。转移性癌细胞比非转移性癌细胞更具可塑性,因为前者必须在原发肿瘤发展的微环境中生存,此外,它们必须在转移器官的微环境中茁壮成长。代谢重编程不仅需要调整代谢途径本身,还需要调整信号通路,这些信号通路将接收并服从细胞外指令,指挥代谢适应。许多不同的参与者在癌症代谢适应性中起着至关重要的作用,从初始信号刺激开始,经历基因的激活或抑制,直到表现出表型。新表型将允许导入和消耗有机化合物,这些化合物可用于能量和生物量的产生,并将代谢产物输出,这些产物无用或必须分泌以进一步回收或受控摄取。在代谢网络中,有三个子集的参与者至关重要:(1)有机化合物;(2)跨膜转运蛋白;(3)酶。这一章将展示这三个元素之间相互作用的“法老”意图,试图简化并同时展示癌症代谢的复杂视角,强调微环境的协调作用,并突出非癌细胞的影响。