Akter Reshmi, Awais Muhammad, Boopathi Vinothini, Ahn Jong Chan, Yang Deok Chun, Kang Se Chan, Yang Dong Uk, Jung Seok-Kyu
Graduate School of Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Gyeonggido, Republic of Korea.
AIBIOME, 6, Jeonmin-ro 30beon-gil, Yuseong-gu 34214, Daejeon, Republic of Korea.
ACS Pharmacol Transl Sci. 2024 Feb 2;7(3):560-569. doi: 10.1021/acsptsci.3c00301. eCollection 2024 Mar 8.
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.
肥胖是一种公认的癌症风险因素,对癌症的发病率和死亡率均有重大影响。然而,将脂肪组织与癌细胞代谢联系起来的复杂分子机制尚未完全明确。本综述探讨了肿瘤能量代谢研究的历史背景,追溯其起源至1920年奥托·瓦尔堡的开创性工作。瓦尔堡发现的“瓦尔堡效应”,即癌细胞即使在有氧存在的情况下也倾向于无氧糖酵解,为理解癌症代谢奠定了基础。在此基础上,2009年出现了“反向瓦尔堡效应”,阐明了有氧糖酵解在癌症相关成纤维细胞(CAFs)中的作用及其对肿瘤微环境中乳酸积累的贡献,随后乳酸成为癌细胞的代谢底物。相比之下,在高肥胖环境中,癌细胞表现出一种独特的代谢转变,称为“瓦尔堡效应反转”。这种现象不同于依赖基质的反向瓦尔堡效应,它依赖于肥胖环境中增加的营养丰度,导致乳酸生成葡萄糖作为代谢底物。本综述强调了肥胖与肿瘤增殖加剧和侵袭性增加之间的关联,引入“瓦尔堡效应反转”作为一种源于肥胖环境中代谢格局改变的新机制。这里提出的见解为治疗探索开辟了有前景的途径,为创新癌症治疗策略的开发提供了新的视角和机会。