The role of autophagy in regulating metabolism in the tumor microenvironment

被引:10
|
作者
Zhang, Panpan [2 ]
Cheng, Shanshan [2 ]
Sheng, Xiaonan [3 ]
Dai, Huijuan [3 ]
He, Kang [1 ]
Du, Yueyao [3 ]
机构
[1] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Liver Surg, Shanghai 200127, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Dept Gynecol & Obstet, Shanghai Key Lab Gynecol Oncol,Sch Med, Shanghai 200127, Peoples R China
[3] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Breast Surg, 1630 Dongfang Rd, Shanghai 200127, Peoples R China
基金
中国国家自然科学基金;
关键词
Autophagy; Metabolism; Therapeutic targets; Tumor; Tumor microenvironment; CANCER-ASSOCIATED FIBROBLASTS; NEUTROPHIL EXTRACELLULAR TRAPS; BREAST-CANCER; OXIDATIVE STRESS; ADIPOSE-TISSUE; CELLS; GLYCOLYSIS; HYPOXIA; METASTASIS; GLUTAMINE;
D O I
10.1016/j.gendis.2021.10.010
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
Autophagy, as a special programmed cell death, is a critical degradative process that eliminates intracellular abnormal proteins or damage organelles to balance cell energy and favor cell metabolism with autophagy-related (ATG) proteins. Autophagy activation is being increasingly recognized as an essential hallmark in tumorigenesis through influencing the metabolism of stromal cells in the tumor microenvironment (TME) which comprises of tumor cells, cancer-associated fibroblasts (CAFs), cancer-associated endothelial cells (CAEs), immune cells and adipocytes. Tumor cells can reuse autophagy-involved recycling to maintain mitochondrial function and energy supply to meet the metabolic demand of their growth and proliferation. However, the mechanism through which autophagy can promote a crosstalk between tumor and stroma cells is not clear. Reprogramed metabolism is one of the main characteristics of TME leading to higher adaptability of tumor cells with diverse mechanisms. The activation of autophagy has expanded our understanding on the interaction between tumor metabolism and TME. The aim of this review is to report recent advances on the metabolic cross-talk between stromal cells and solid tumor cells induced by autophagy in TME and revealed potential therapeutic targets. (c) 2021 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons. org/licenses/by-nc-nd/4.0/).
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页码:447 / 456
页数:10
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