Rudolf-Zenker-Institute of Experimental Surgery, University Medical Center, Rostock, Germany.
Core Facility Multimodal Small Animal Imaging, University Medical Center, Rostock, Germany.
PLoS One. 2022 Apr 22;17(4):e0266601. doi: 10.1371/journal.pone.0266601. eCollection 2022.
Pancreatic cancer is the fourth leading cause of cancer death, with a 5-year survival rate of 10%. A stagnant high mortality rate over the last decades highlights the need for innovative therapeutic approaches. Pancreatic tumors pursue an altered metabolism in order to maintain energy generation under low nutrient influx and hypoxic conditions. Targeting these metabolic strategies might therefore be a reasonable therapeutic approach for pancreatic cancer. One promising agent is CPI- 613, a potent inhibitor of two enzymes of the tricarboxylic acid cycle. The present study evaluated the anti-cancerous efficacy of CPI-613 in combination with galloflavin, a lactate dehydrogenase inhibitor or with alpha-cyano-4-hydroxycinnamic acid, an inhibitor of monocarboxylate transporters. The efficacy of both combination therapies was tested in vitro on one human and two murine pancreatic cancer cell lines and in vivo in an orthotopic pancreatic cancer model. Tumor progression was evaluated by MRI and 18F-FDG PET-CT. Both combinatorial treatments demonstrated in vitro a significant inhibition of pancreatic cancer cell proliferation and induction of cell death. In contrast to the in vitro results, both combination therapies did not significantly reduce tumor growth in vivo. The in vitro results suggest that a combined inhibition of different metabolic pathways might be a promising approach for cancer therapy. However, the in vivo experiments indicate that applying a higher dosage or using other drugs targeting these metabolic pathways might be more promising.
胰腺癌是癌症死亡的第四大主要原因,其 5 年生存率为 10%。过去几十年来,死亡率一直居高不下,这凸显了需要创新的治疗方法。为了在低营养摄入和缺氧条件下维持能量生成,胰腺肿瘤会采用改变代谢的方式。因此,针对这些代谢策略可能是治疗胰腺癌的一种合理方法。一种有前途的药物是 CPI-613,它是三羧酸循环的两种酶的有效抑制剂。本研究评估了 CPI-613 与大黄素、乳酸脱氢酶抑制剂或 alpha-氰基-4-羟基肉桂酸(单羧酸转运蛋白抑制剂)联合使用的抗癌疗效。在体外,这两种联合疗法在一种人源和两种鼠源胰腺癌细胞系中进行了测试,在原位胰腺癌细胞模型中进行了体内测试。通过 MRI 和 18F-FDG PET-CT 评估肿瘤进展。两种组合疗法均在体外显著抑制胰腺癌细胞增殖并诱导细胞死亡。与体外结果相反,两种联合疗法在体内均未显著抑制肿瘤生长。体外结果表明,联合抑制不同的代谢途径可能是癌症治疗的一种有前途的方法。然而,体内实验表明,使用更高剂量或使用其他针对这些代谢途径的药物可能更有前途。