Lipid metabolism in cancer progression and therapeutic strategies

被引:224
作者
Fu, Yan [1 ,2 ,3 ]
Zou, Tiantian [1 ,2 ,3 ]
Shen, Xiaotian [1 ,2 ,3 ]
Nelson, Peter J. [4 ]
Li, Jiahui [5 ]
Wu, Chao [6 ]
Yang, Jimeng [1 ,2 ,3 ]
Zheng, Yan [1 ,2 ,3 ]
Bruns, Christiane [5 ]
Zhao, Yue [5 ]
Qin, Lunxiu [1 ,2 ,3 ]
Dong, Qiongzhu [1 ,2 ,3 ]
机构
[1] Fudan Univ, Dept Gen Surg, Huashan Hosp, Shanghai, Peoples R China
[2] Fudan Univ, Canc Metastasis Inst, Shanghai, Peoples R China
[3] Fudan Univ, Inst Biomed Sci, 131 DongAn Rd, Shanghai 200032, Peoples R China
[4] Ludwig Maximilian Univ LMU, Med Clin & Policlin 4, Munich, Germany
[5] Univ Hosp Cologne, Gen Visceral & Canc Surg, D-50937 Cologne, Germany
[6] Shanghai Jiao Tong Univ, Ruijin Hosp, Dept Gen Surg, Sch Med, Shanghai, Peoples R China
来源
MEDCOMM | 2021年 / 2卷 / 01期
基金
中国国家自然科学基金;
关键词
cancer; lipid metabolism; mechanism; microenvironment; therapeutic strategy; FATTY-ACID SYNTHASE; STEAROYL-COA-DESATURASE; ATP CITRATE LYASE; SPHINGOSINE KINASE 1; ELEMENT-BINDING PROTEINS; HUMAN COLORECTAL-CANCER; CD8(+) T-CELLS; PROSTATE-CANCER; BREAST-CANCER; PHOSPHOLIPASE-D;
D O I
10.1002/mco2.27
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Dysregulated lipid metabolism represents an important metabolic alteration in cancer. Fatty acids, cholesterol, and phospholipid are the three most prevalent lipids that act as energy producers, signaling molecules, and source material for the biogenesis of cell membranes. The enhanced synthesis, storage, and uptake of lipids contribute to cancer progression. The rewiring of lipid metabolism in cancer has been linked to the activation of oncogenic signaling pathways and cross talk with the tumor microenvironment. The resulting activity favors the survival and proliferation of tumor cells in the harsh conditions within the tumor. Lipid metabolism also plays a vital role in tumor immunogenicity via effects on the function of the noncancer cells within the tumor microenvironment, especially immune-associated cells. Targeting altered lipid metabolism pathways has shown potential as a promising anticancer therapy. Here, we review recent evidence implicating the contribution of lipid metabolic reprogramming in cancer to cancer progression, and discuss the molecular mechanisms underlying lipid metabolism rewiring in cancer, and potential therapeutic strategies directed toward lipid metabolism in cancer. This review sheds new light to fully understanding of the role of lipid metabolic reprogramming in the context of cancer and provides valuable clues on therapeutic strategies targeting lipid metabolism in cancer.
引用
收藏
页码:27 / 59
页数:33
相关论文
共 331 条
[1]   Hypoxia, lipids, and cancer: surviving the harsh tumor microenvironment [J].
Ackerman, Daniel ;
Simon, M. Celeste .
TRENDS IN CELL BIOLOGY, 2014, 24 (08) :472-478
[2]   The Fatty Acid Synthase Inhibitor Orlistat Reduces the Growth and Metastasis of Orthotopic Tongue Oral Squamous Cell Carcinomas [J].
Agostini, Michelle ;
Almeida, Luciana Y. ;
Bastos, Debora C. ;
Ortega, Rose M. ;
Moreira, Fernanda S. ;
Seguin, Fabiana ;
Zecchin, Karina G. ;
Raposo, Helena F. ;
Oliveira, Helena C. F. ;
Amoedo, Nivea D. ;
Salo, Tuula ;
Coletta, Ricardo D. ;
Graner, Edgard .
MOLECULAR CANCER THERAPEUTICS, 2014, 13 (03) :585-595
[3]   Exogenous lipid uptake induces metabolic and functional reprogramming of tumor-associated myeloid-derived suppressor cells [J].
Al-Khami, Amir A. ;
Zheng, Liqin ;
Del Valle, Luis ;
Hossain, Fokhrul ;
Wyczechowska, Dorota ;
Zabaleta, Jovanny ;
Sanchez, Maria D. ;
Dean, Matthew J. ;
Rodriguez, Paulo C. ;
Ochoa, Augusto C. .
ONCOIMMUNOLOGY, 2017, 6 (10)
[4]   Snail1-Dependent Activation of Cancer-Associated Fibroblast Controls Epithelial Tumor Cell Invasion and Metastasis [J].
Alba-Castellon, Lorena ;
Olivera-Salguero, Ruben ;
Mestre-Farrera, Aida ;
Pena, Raul ;
Herrera, Mercedes ;
Bonilla, Felix ;
Ignacio Casal, J. ;
Baulida, Josep ;
Pena, Cristina ;
Garcia de Herreros, Antonio .
CANCER RESEARCH, 2016, 76 (21) :6205-6217
[5]   Bile Acids Activate YAP to Promote Liver Carcinogenesis [J].
Anakk, Sayeepriyadarshini ;
Bhosale, Manoj ;
Schmidt, Valentina A. ;
Johnson, Randy L. ;
Finegold, Milton J. ;
Moore, David D. .
CELL REPORTS, 2013, 5 (04) :1060-1069
[6]   The LATS2 tumor suppressor inhibits SREBP and suppresses hepatic cholesterol accumulation [J].
Aylon, Yael ;
Gershoni, Anat ;
Rotkopf, Ron ;
Biton, Inbal E. ;
Porat, Ziv ;
Koh, Anna P. ;
Sun, Xiaochen ;
Lee, Youngmin ;
Fiel, Maria-Isabel ;
Hoshida, Yujin ;
Friedman, Scott L. ;
Johnson, Randy L. ;
Oren, Moshe .
GENES & DEVELOPMENT, 2016, 30 (07) :786-797
[7]   5-aminosalicylic acid inhibits cell cycle progression in a phospholipase D dependent manner in colorectal cancer [J].
Baan, Bart ;
Dihal, Ashwin A. ;
Hoff, Eva ;
Bos, Carina L. ;
Voorneveld, Philip W. ;
Koelink, Pim J. ;
Wildenberg, Manon E. ;
Muncan, Vanesa ;
Heijmans, Jarom ;
Verspaget, Hein W. ;
Richel, Dick J. ;
Hardwick, James C. H. ;
Hommes, Daniel W. ;
Peppelenbosch, Maikel P. ;
van den Brink, Gijs R. .
GUT, 2012, 61 (12) :1708-1715
[8]   The cholesterol metabolite 27 hydroxycholesterol facilitates breast cancer metastasis through its actions on immune cells [J].
Baek, Amy E. ;
Yu, Yen-Rei A. ;
He, Sisi ;
Wardell, Suzanne E. ;
Chang, Ching-Yi ;
Kwon, Sanghoon ;
Pillai, Ruchita V. ;
McDowell, Hannah B. ;
Thompson, J. Will ;
Dubois, Laura G. ;
Sullivan, Patrick M. ;
Kemper, Jongsook K. ;
Gunn, Michael D. ;
McDonnell, Donald P. ;
Nelson, Erik R. .
NATURE COMMUNICATIONS, 2017, 8
[9]   Targeting PPAR ligands as possible approaches for metabolic reprogramming of T cells in cancer immunotherapy [J].
Bahrambeigi, Saman ;
Molaparast, Morteza ;
Sohrabi, Farahnaz ;
Seifi, Lachin ;
Faraji, Alireza ;
Fani, Saba ;
Shafiei-Irannejad, Vahid .
IMMUNOLOGY LETTERS, 2020, 220 :32-37
[10]   The role of miR-122 in the dysregulation of glucose-6-phosphate dehydrogenase (G6PD) expression in hepatocellular cancer [J].
Barajas, Juan M. ;
Reyes, Ryan ;
Guerrero, Maria J. ;
Jacob, Samson T. ;
Motiwala, Tasneem ;
Ghoshal, Kalpana .
SCIENTIFIC REPORTS, 2018, 8