4.8 Article

Targeting Cancer Metabolism Plasticity with JX06 Nanoparticles via Inhibiting PDK1 Combined with Metformin for Endometrial Cancer Patients with Diabetes

Journal

ADVANCED SCIENCE
Volume 9, Issue 8, Pages -

Publisher

WILEY
DOI: 10.1002/advs.202104472

Keywords

cell metabolic reprogramming; diabetes; endometrial cancer; high glucose; metformin; PDK1

Funding

  1. National Key Technology R&D Program of China [2019YFC1005200, 2019YFC1005201]
  2. National Natural Science Foundation of China [82072861, 81672571, 81874108]
  3. Natural Science Foundation of Beijing [7202213]

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This study found that diabetes is closely related to endometrial cancer and there is currently no effective treatment for patients with both conditions. Through experiments, a new drug (JX06-NPs) that disrupts cancer metabolism was discovered to significantly inhibit the growth of endometrial cancer cells, with better results when combined with metformin. This study provides a new adjuvant therapy for patients with diabetes and endometrial cancer.
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+).

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