背景(考古学)
癌细胞
内吞循环
细胞生物学
肿瘤微环境
细胞外
癌症
内吞作用
生物
免疫系统
胞饮病
细胞
生物化学
免疫学
遗传学
古生物学
作者
Joseph Puccini,Michael A. Badgley,Dafna Bar‐Sagi
标识
DOI:10.1016/j.trecan.2021.09.004
摘要
By delivering vital metabolic substrates to cancer cells, macropinocytosis presents an attractive and targetable vulnerability in tumors. Macropinocytosis facilitates the uptake of a wide assortment of extracellular macromolecules and metabolites in addition to protein. Emerging evidence illustrates that many different tumor types engage in macropinocytosis through multiple oncogenic drivers. The delivery of therapeutic agents via macropinocytosis offers an alternative approach for selective targeting of tumor cells. Macropinocytosis, an evolutionarily conserved endocytic mechanism that mediates non-specific fluid-phase uptake, is potently upregulated by various oncogenic pathways. It is now well appreciated that high macropinocytic activity is a hallmark of many human tumors, which use this adaptation to scavenge extracellular nutrients for fueling cell growth. In the context of the nutrient-scarce tumor microenvironment, this process provides tumor cells with metabolic flexibility. However, dependence on this scavenging mechanism also illuminates a potential metabolic vulnerability. As such, there is a great deal of interest in understanding the molecular underpinnings of macropinocytosis. In this review, we will discuss the most recent advances in characterizing macropinocytosis: the pathways that regulate it, its contribution to the metabolic fitness of cancer cells, and its therapeutic potential. Macropinocytosis, an evolutionarily conserved endocytic mechanism that mediates non-specific fluid-phase uptake, is potently upregulated by various oncogenic pathways. It is now well appreciated that high macropinocytic activity is a hallmark of many human tumors, which use this adaptation to scavenge extracellular nutrients for fueling cell growth. In the context of the nutrient-scarce tumor microenvironment, this process provides tumor cells with metabolic flexibility. However, dependence on this scavenging mechanism also illuminates a potential metabolic vulnerability. As such, there is a great deal of interest in understanding the molecular underpinnings of macropinocytosis. In this review, we will discuss the most recent advances in characterizing macropinocytosis: the pathways that regulate it, its contribution to the metabolic fitness of cancer cells, and its therapeutic potential.
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