| PDK4-dependent hypercatabolism and lactate production of senescent cells promotes cancer malignancy |
| 論文作者 |
Dou, XF; Fu, Q; Long, QL; Liu, SN; Zou, YJ; Fu, D; Xu, QX; Jiang, ZR; Ren, XH; Zhang, GL; Wei, XL; Li, QF; Campisi, J; Zhao, YZ; Sun, Y |
| 期刊/會(huì)議名稱 |
NATURE METABOLISM |
| 論文年度 |
2023 |
| 論文類別 |
Article; Early Access |
| 摘要 |
Senescent cells remain metabolically active, but their metabolic landscape and resulting implications remain underexplored. Here, we report upregulation of pyruvate dehydrogenase kinase 4 (PDK4) upon senescence, particularly in some stromal cell lines. Senescent cells display a PDK4-dependent increase in aerobic glycolysis and enhanced lactate production but maintain mitochondrial respiration and redox activity, thus adopting a special form of metabolic reprogramming. Medium from PDK4+ stromal cells promotes the malignancy of recipient cancer cells in vitro, whereas inhibition of PDK4 causes tumor regression in vivo. We find that lactate promotes reactive oxygen species production via NOX1 to drive the senescence-associated secretory phenotype, whereas PDK4 suppression reduces DNA damage severity and restrains the senescence-associated secretory phenotype. In preclinical trials, PDK4 inhibition alleviates physical dysfunction and prevents age-associated frailty. Together, our study confirms the hypercatabolic nature of senescent cells and reveals a metabolic link between cellular senescence, lactate production, and possibly, age-related pathologies, including but not limited to cancer. PDK4-dependent lactate production by senescent stromal cells is shown to promote cancer growth and drug resistance and might have a broader role in the emergence of age-associated diseases. |
| 影響因子 |
20.8 |
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