Evo312: An Evodiamine Analog and Novel PKCβI Inhibitor with Potent Antitumor Activity in Gemcitabine-Resistant Pancreatic Cancer.
Eun Seo BaeJunhwa HongYijae LimWoong Sub ByunSimin ChunSuckchang HongSang-Kook LeePublished in: Journal of medicinal chemistry (2024)
As an obstinate cancer pancreatic cancer (PC) poses a major challenge due to limited treatment options which include resection surgery, radiation therapy, and gemcitabine-based chemotherapy. In cancer cells, protein kinase C βI (PKCβI) participates in diverse cellular processes, including cell proliferation, invasion, and apoptotic pathways. In the present study, we created a scaffold to develop PKCβI inhibitors using evodiamine-based synthetic molecules. Among the candidate inhibitors, Evo312 exhibited the highest antiproliferative efficacy against PC cells, PANC-1, and acquired gemcitabine-resistant PC cells, PANC-GR. Additionally, Evo312 robustly inhibited PKCβI activity. Mechanistically, Evo312 effectively suppressed the upregulation of PKCβI protein expression, leading to the induction of cell cycle arrest and apoptosis in PANC-GR cells. Furthermore, Evo312 exerted an antitumor activity in a PANC-GR cell-implanted xenograft mouse model. These findings position Evo312 as a promising lead compound for overcoming gemcitabine resistance in PC through novel mechanisms.
Keyphrases
- cell cycle arrest
- cell death
- protein kinase
- locally advanced
- pi k akt
- cell proliferation
- radiation therapy
- mouse model
- signaling pathway
- rectal cancer
- squamous cell carcinoma
- papillary thyroid
- oxidative stress
- stem cells
- anti inflammatory
- poor prognosis
- acute coronary syndrome
- mesenchymal stem cells
- bone marrow
- young adults
- radiation induced