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Tumor metabolism, cancer cell transporters, and microenvironmental resistance

机译:肿瘤新陈代谢,癌细胞转运蛋白和微环境抗性

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摘要

Cancer cells reprogram their metabolic machineries to enter into permanent glycolytic pathways. The full reason for such reprogramming takes place is unclear. However, this metabolic switch is not made in vain for the lactate that is generated and exported outside cells is reused by other cells. This results in the generation of a pH gradient between the low extracellular pH that is acidic (pHe) and the higher cytosolic alkaline or near neutral pH (pHi) environments that are tightly regulated by the overexpression of several pumps and ion channels (e.g. NHE-1, MCT-1, V-ATPase, CA9, and CA12). The generation of this unique pH gradient serves as a determining factor in defining "tumor fitness''. Tumor fitness is the capacity of the tumor to invade and metastasize due to its ability to reduce the efficiency of the immune system and confer resistance to chemotherapy. In this article, we highlight the importance of tumor microenvironment in mediating the failure of chemotherapeutic agents.
机译:癌细胞重新编程其代谢机制,进入永久性糖酵解途径。这种重新编程的全部原因尚不清楚。然而,这种代谢转换并不是徒劳的,因为细胞外产生和输出的乳酸被其他细胞重复利用。这导致细胞外pH值较低的酸性环境(pHe)和较高的胞质碱性或近中性环境(pHi)之间产生pH梯度,这些环境受到多个泵和离子通道(例如NHE-1、MCT-1、V-ATP酶、CA9和CA12)过度表达的严格调节。这种独特的pH梯度的产生是定义“肿瘤适合度”的决定因素。肿瘤适合度是指肿瘤侵袭和转移的能力,因为它能够降低免疫系统的效率并对化疗产生耐药性。在本文中,我们强调了肿瘤微环境在介导化疗药物失败中的重要性。

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