Functions of autophagy in the tumor microenvironment and cancer metastasis

被引:210
|
作者
Mowers, Erin E. [1 ,2 ,3 ]
Sharifi, Marina N. [1 ,2 ,4 ]
Macleod, Kay F. [1 ,2 ,5 ]
机构
[1] Univ Chicago, Ben May Dept Canc Res, 929 East 57th St, Chicago, IL 60637 USA
[2] Comm Canc Biol, Chicago, IL USA
[3] Interdisciplinary Scientist Training Program, Chicago, IL USA
[4] Med Scientist Training Program, Chicago, IL USA
[5] Univ Chicago, Chicago, IL 60637 USA
关键词
autophagy; invasion; metastasis; mitophagy; tumor cell migration; tumor microenvironment; tumor stem cells; EPITHELIAL-MESENCHYMAL TRANSITION; PANCREATIC STELLATE CELLS; FOCAL ADHESION KINASE; STEM-CELLS; TARGETING AUTOPHAGY; INHIBITS AUTOPHAGY; BONE-MARROW; AMINO-ACIDS; PROMOTES; GROWTH;
D O I
10.1111/febs.14388
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macro-autophagy is an ancient and highly conserved self-degradative process that plays a homeostatic role in normal cells by eliminating organelles, pathogens, and protein aggregates. Autophagy, as it is routinely referred to, also allows cells to maintain metabolic sufficiency and survive under conditions of nutrient stress by recycling the by-products of autophagic degradation, such as fatty acids, amino acids, and nucleotides. Tumor cells are more reliant than normal cells on autophagy for survival in part due to their rapid growth rate, altered metabolism, and nutrient-deprived growth environment. How this dependence of tumor cells on autophagy affects their progression to malignancy and metastatic disease is an area of increasing research focus. Here, we review recent work identifying critical functions for autophagy in tumor cell migration and invasion, tumor stem cell maintenance and therapy resistance, and cross-talk between tumor cells and their microenvironment.
引用
收藏
页码:1751 / 1766
页数:16
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