TY - JOUR
T1 - Inversion of the Warburg Effect
T2 - Unraveling the Metabolic Nexus between Obesity and Cancer
AU - Akter, Reshmi
AU - Awais, Muhammad
AU - Boopathi, Vinothini
AU - Ahn, Jong Chan
AU - Yang, Deok Chun
AU - Kang, Se Chan
AU - Yang, Dong Uk
AU - Jung, Seok Kyu
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/3/8
Y1 - 2024/3/8
N2 - Obesity is a well-established risk factor for cancer, significantly impacting both cancer incidence and mortality. However, the intricate molecular mechanisms connecting adipose tissue to cancer cell metabolism are not fully understood. This Review explores the historical context of tumor energy metabolism research, tracing its origins to Otto Warburg’s pioneering work in 1920. Warburg’s discovery of the “Warburg effect”, wherein cancer cells prefer anaerobic glycolysis even in the presence of oxygen, laid the foundation for understanding cancer metabolism. Building upon this foundation, the “reverse Warburg effect” emerged in 2009, elucidating the role of aerobic glycolysis in cancer-associated fibroblasts (CAFs) and its contribution to lactate accumulation in the tumor microenvironment, subsequently serving as a metabolic substrate for cancer cells. In contrast, within high-adiposity contexts, cancer cells exhibit a unique metabolic shift termed the “inversion of the Warburg effect”. This phenomenon, distinct from the stromal-dependent reverse Warburg effect, relies on increased nutrient abundance in obesity environments, leading to the generation of glucose from lactate as a metabolic substrate. This Review underscores the heightened tumor proliferation and aggressiveness associated with obesity, introducing the “inversion of the Warburg effect” as a novel mechanism rooted in the altered metabolic landscape within an obese milieu. The insights presented here open promising avenues for therapeutic exploration, offering fresh perspectives and opportunities for the development of innovative cancer treatment strategies.
AB - Obesity is a well-established risk factor for cancer, significantly impacting both cancer incidence and mortality. However, the intricate molecular mechanisms connecting adipose tissue to cancer cell metabolism are not fully understood. This Review explores the historical context of tumor energy metabolism research, tracing its origins to Otto Warburg’s pioneering work in 1920. Warburg’s discovery of the “Warburg effect”, wherein cancer cells prefer anaerobic glycolysis even in the presence of oxygen, laid the foundation for understanding cancer metabolism. Building upon this foundation, the “reverse Warburg effect” emerged in 2009, elucidating the role of aerobic glycolysis in cancer-associated fibroblasts (CAFs) and its contribution to lactate accumulation in the tumor microenvironment, subsequently serving as a metabolic substrate for cancer cells. In contrast, within high-adiposity contexts, cancer cells exhibit a unique metabolic shift termed the “inversion of the Warburg effect”. This phenomenon, distinct from the stromal-dependent reverse Warburg effect, relies on increased nutrient abundance in obesity environments, leading to the generation of glucose from lactate as a metabolic substrate. This Review underscores the heightened tumor proliferation and aggressiveness associated with obesity, introducing the “inversion of the Warburg effect” as a novel mechanism rooted in the altered metabolic landscape within an obese milieu. The insights presented here open promising avenues for therapeutic exploration, offering fresh perspectives and opportunities for the development of innovative cancer treatment strategies.
KW - Cancer
KW - Inversion of Warburg effect
KW - Obesity
KW - Reverse Warburg effect
KW - Warburg effect
UR - http://www.scopus.com/inward/record.url?scp=85184871129&partnerID=8YFLogxK
U2 - 10.1021/acsptsci.3c00301
DO - 10.1021/acsptsci.3c00301
M3 - Review article
AN - SCOPUS:85184871129
SN - 2575-9108
VL - 7
SP - 560
EP - 569
JO - ACS Pharmacology and Translational Science
JF - ACS Pharmacology and Translational Science
IS - 3
ER -