Li Dandan, Chu Jiaxin, Yan Yan, Xu Wenjun, Zhu Xingchun, Sun Yun, Ding Haofeng, Ren Li, Zhu Bo
Department of Pathology, Bengbu Medical University, Bengbu 233000, China.
College of Clinical Medicine, Bengbu Medical University, Bengbu 233000, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2025 May 20;45(5):1039-1046. doi: 10.12122/j.issn.1673-4254.2025.05.17.
To investigate the effect of curcumin on lipid metabolism in non-small cell lung cancer (NSCLC) and its molecular mechanism.
The inhibitory effect of curcumin (0-70 μmol/L) on proliferation of A549 and H1299 cells was assessed using MTT assay, and 20 and 40 μmol/L curcumin was used in the subsequent experiments. The effect of curcumin on lipid metabolism was evaluated using cellular uptake assay, wound healing assay, triglyceride (TG)/free fatty acid (NEFA) measurements, and Oil Red O staining. Western blotting was performed to detect the expressions of PGC-1α, PPAR-α, and HIF-1α in curcumin-treated cells. Network pharmacology was used to predict the metabolic pathways, and the results were validated by Western blotting. In a nude mouse model bearing A549 cell xenograft, the effects of curcumin (20 mg/kg) on tumor growth and lipid metabolism were assessed by measuring tumor weight and observing the changes in intracellular lipid droplets.
Curcumin concentration-dependently inhibited the proliferation of A549 and H1299 cells and significantly reduced TG and NEFA levels and intracellular lipid droplets. Western blotting revealed that curcumin significantly upregulated PGC-1α and PPAR‑α expressions in the cells. KEGG pathway enrichment analysis predicted significant involvement of the HIF-1 signaling pathway in curcumin-treated NSCLC, suggesting a potential interaction between HIF-1α and PPAR‑α. Western blotting confirmed that curcumin downregulated the expression of HIF-1α. In the tumor-bearing mice, curcumin treatment caused significant reduction of the tumor weight and the number of lipid droplets in the tumor cells.
Curcumin inhibits NSCLC cell proliferation and lipid metabolism by downregulating the HIF-1α pathway.
探讨姜黄素对非小细胞肺癌(NSCLC)脂质代谢的影响及其分子机制。
采用MTT法评估姜黄素(0 - 70 μmol/L)对A549和H1299细胞增殖的抑制作用,后续实验采用20和40 μmol/L的姜黄素。通过细胞摄取实验、伤口愈合实验、甘油三酯(TG)/游离脂肪酸(NEFA)测定和油红O染色评估姜黄素对脂质代谢的影响。进行蛋白质免疫印迹法检测姜黄素处理细胞中PGC - 1α、PPAR - α和HIF - 1α的表达。利用网络药理学预测代谢途径,并通过蛋白质免疫印迹法验证结果。在携带A549细胞异种移植的裸鼠模型中,通过测量肿瘤重量和观察细胞内脂滴变化评估姜黄素(20 mg/kg)对肿瘤生长和脂质代谢的影响。
姜黄素浓度依赖性地抑制A549和H1299细胞的增殖,并显著降低TG和NEFA水平以及细胞内脂滴。蛋白质免疫印迹法显示,姜黄素显著上调细胞中PGC - 1α和PPAR - α的表达。KEGG通路富集分析预测HIF - 1信号通路在姜黄素处理的NSCLC中显著参与,提示HIF - 1α与PPAR - α之间可能存在相互作用。蛋白质免疫印迹法证实姜黄素下调HIF - 1α的表达。在荷瘤小鼠中,姜黄素治疗导致肿瘤重量显著减轻以及肿瘤细胞中脂滴数量减少。
姜黄素通过下调HIF - 1α通路抑制NSCLC细胞增殖和脂质代谢。