Anti-proliferative and apoptotic effect of cannabinoids on human pancreatic ductal adenocarcinoma xenograft in BALB/c nude mice model

Sci Rep. 2024 Mar 18;14(1):6515. doi: 10.1038/s41598-024-55307-y.

Abstract

Human pancreatic ductal adenocarcinoma (PDAC) is a highly malignant and lethal tumor of the exocrine pancreas. Cannabinoids extracted from the hemp plant Cannabis sativa have been suggested as a potential therapeutic agent in several human tumors. However, the anti-tumor effect of cannabinoids on human PDAC is not entirely clarified. In this study, the anti-proliferative and apoptotic effect of cannabinoid solution (THC:CBD at 1:6) at a dose of 1, 5, and 10 mg/kg body weight compared to the negative control (sesame oil) and positive control (5-fluorouracil) was investigated in human PDAC xenograft nude mice model. The findings showed that cannabinoids significantly decreased the mitotic cells and mitotic/apoptotic ratio, meanwhile dramatically increased the apoptotic cells. Parallelly, cannabinoids significantly downregulated Ki-67 and PCNA expression levels. Interestingly, cannabinoids upregulated BAX, BAX/BCL-2 ratio, and Caspase-3, meanwhile, downregulated BCL-2 expression level and could not change Caspase-8 expression level. These findings suggest that cannabinoid solution (THC:CBD at 1:6) could inhibit proliferation and induce apoptosis in human PDAC xenograft models. Cannabinoids, including THC:CBD, should be further studied for use as the potent PDCA therapeutic agent in humans.

Keywords: Anti-proliferation; Apoptosis; Cannabis; Nude mouse xenograft model; Pancreatic adenocarcinoma.

MeSH terms

  • Animals
  • Cannabinoids* / pharmacology
  • Cannabinoids* / therapeutic use
  • Cannabis*
  • Carcinoma, Pancreatic Ductal* / drug therapy
  • Heterografts
  • Humans
  • Mice
  • Mice, Nude
  • Pancreatic Neoplasms* / drug therapy
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein

Substances

  • Cannabinoids
  • bcl-2-Associated X Protein
  • Proto-Oncogene Proteins c-bcl-2