Targeting Cancer Metabolism Plasticity with JX06 Nanoparticles via Inhibiting PDK1 Combined with Metformin for Endometrial Cancer Patients with Diabetes
Xiao Yang, Yuan Cheng, Jingyi Zhou, Lingpu Zhang, Xingchen Li, Zhiqi Wang, Shenyi Yin, Lirong Zhai, Ting Huang, Xiaotong Wu, Boqiang Shen, Yangyang Dong, Lijun Zhao, Yujing Chi, Yuanyuan Jia, Jiaqi Wang, Jiaqi Wang, Yijiao He, Xiying Dong, Haihua Xiao, Jianliu Wang, Jianliu Wang
Abstract
Abstract Diabetes is closely related to the occurrence of endometrial cancer (EC) and its poor prognosis. However, there is no effective clinical treatment for EC patients with diabetes (patient EC+/dia+ ). To explore new therapeutic targets, Ishikawa is cultured with high glucose (Ishikawa HG ) mimicking hyperglycemia in patient EC+/dia+ . Subsequently, it is discovered that Ishikawa HG exhibits glucose metabolic reprogramming characterized by increased glycolysis and decreased oxidative phosphorylation. Further, pyruvate dehydrogenase kinase 1 (PDK1) is identified to promote glycolysis of Ishikawa HG by proteomics. Most importantly, JX06, a novel PDK1 inhibitor combined metformin (Met) significantly inhibits Ishikawa HG proliferation though Ishikawa HG is resistant to Met. Furthermore, a reduction‐sensitive biodegradable polymer is adopted to encapsulate JX06 to form nanoparticles (JX06‐NPs) for drug delivery. It is found that in vitro JX06‐NPs have better inhibitory effect on the growth of Ishikawa HG as well as patient‐derived EC cells (PDC) than JX06. Additionally, it is found that JX06‐NPs can accumulate to the tumor of EC‐bearing mouse with diabetes (mice EC+/dia+ ) after intravenous injection, and JX06‐NPs combined Met can significantly inhibit tumor growth of mice EC+/dia+ . Taken together, the study demonstrates that the combination of JX06‐NPs and Met can target the cancer metabolism plasticity, which significantly inhibits the growth of EC, thereby provides a new adjuvant therapy for patients EC+/dia+ .