Targeting Glutamine Metabolism for Cancer Treatment

被引:249
作者
Choi, Yeon-Kyung [1 ]
Park, Keun-Gyu [1 ]
机构
[1] Kyungpook Natl Univ, Sch Med, Dept Internal Med, Daegu 41944, South Korea
关键词
Cancer; Glutamine; Anaplerosis; Redox homeostasis; PHOSPHATE-ACTIVATED GLUTAMINASE; OXIDATIVE STRESS; CELL BIOLOGY; TUMOR-GROWTH; AUTOPHAGY; MTOR; RESISTANCE; EXPRESSION; SURVIVAL; GLS2;
D O I
10.4062/biomolther.2017.178
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
Rapidly proliferating cancer cells require energy and cellular building blocks for their growth and ability to maintain redox balance. Many studies have focused on understanding how cancer cells adapt their nutrient metabolism to meet the high demand of anabolism required for proliferation and maintaining redox balance. Glutamine, the most abundant amino acid in plasma, is a well-known nutrient used by cancer cells to increase proliferation as well as survival under metabolic stress conditions. In this review, we provide an overview of the role of glutamine metabolism in cancer cell survival and growth and highlight the mechanisms by which glutamine metabolism affects cancer cell signaling. Furthermore, we summarize the potential therapeutic approaches of targeting glutamine metabolism for the treatment of numerous types of cancer.
引用
收藏
页码:19 / 28
页数:10
相关论文
共 86 条
[1]   Redox control of glutamine utilization in cancer [J].
Alberghina, L. ;
Gaglio, D. .
CELL DEATH & DISEASE, 2014, 5 :e1561-e1561
[2]   From Krebs to clinic: glutamine metabolism to cancer therapy (vol 16, pg 619, 2016) [J].
Altman, Brian J. ;
Stine, Zachary E. ;
Dang, Chi V. .
NATURE REVIEWS CANCER, 2016, 16 (12) :773-773
[3]   Resistance to BRAF inhibitors induces glutamine dependency in melanoma cells [J].
Baenke, Franziska ;
Chaneton, Barbara ;
Smith, Matthew ;
Van Den Broek, Niels ;
Hogan, Kate ;
Tang, Haoran ;
Viros, Amaya ;
Martin, Matthew ;
Galbraith, Laura ;
Girotti, Maria R. ;
Dhomen, Nathalie ;
Gottlieb, Eyal ;
Marais, Richard .
MOLECULAR ONCOLOGY, 2016, 10 (01) :73-84
[4]   The two TORCs and Akt [J].
Bhaskar, Prashanth T. ;
Hay, Nissim .
DEVELOPMENTAL CELL, 2007, 12 (04) :487-502
[5]   Amino Acid Transporters in Cancer and Their Relevance to "Glutamine Addiction": Novel Targets for the Design of a New Class of Anticancer Drugs [J].
Bhutia, Yangzom D. ;
Babu, Ellappan ;
Ramachandran, Sabarish ;
Ganapathy, Vadivel .
CANCER RESEARCH, 2015, 75 (09) :1782-1788
[6]   Metabolic pathways promoting cancer cell survival and growth [J].
Boroughs, Lindsey K. ;
DeBerardinis, Ralph J. .
NATURE CELL BIOLOGY, 2015, 17 (04) :351-359
[7]   KRAS: feeding pancreatic cancer proliferation [J].
Bryant, Kirsten L. ;
Mancias, Joseph D. ;
Kimmelman, Alec C. ;
Der, Channing J. .
TRENDS IN BIOCHEMICAL SCIENCES, 2014, 39 (02) :91-100
[8]   Alanyl-glutamine consumption modifies the suppressive effect of L-asparaginase on lymphocyte Populations in mice1,2 [J].
Bunpo, Piyawan ;
Murray, Betty ;
Cundiff, Judy ;
Brizius, Emma ;
Aldrich, Carla J. ;
Anthony, Tracy G. .
JOURNAL OF NUTRITION, 2008, 138 (02) :338-343
[9]   A Positive Feedback Loop between Sestrin2 and mTORC2 Is Required for the Survival of Glutamine-Depleted Lung Cancer Cells [J].
Byun, Jun-Kyu ;
Choi, Yeon-Kyung ;
Kim, Ji-Hyun ;
Jeong, Ji Yun ;
Jeon, Hui-Jeon ;
Kim, Mi-Kyung ;
Hwang, Ilseon ;
Lee, Shin-Yup ;
Lee, You Mie ;
Lee, In-Kyu ;
Park, Keun-Gyu .
CELL REPORTS, 2017, 20 (03) :586-599
[10]   Targeting Glutamine Induces Apoptosis: A Cancer Therapy Approach [J].
Chen, Lian ;
Cui, Hengmin .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2015, 16 (09) :22830-22855