Aspirin use and changes in circulating tumor DNA levels in patients with metastatic colorectal cancer

Pak J Pharm Sci. 2024 Jan;37(1):123-128.

Abstract

The study aimed to investigate the effects of aspirin on patients with metastatic colorectal cancer, focusing on circulating tumor DNA levels and bone tissue. Two groups (A and B) of ten patients with osteoporosis were selected for the study. Bone tissue samples were obtained from the patients and cultured under sterile conditions. The aspirin group showed a significant decrease in circulating tumor DNA levels and an increase in bone tissue density compared to the control group. Additionally, osteoblast apoptosis was reduced, while proliferation was enhanced in the aspirin group. The protein pAkt related to the PI3K/Akt signaling pathway was upregulated in the aspirin group. These results indicate that aspirin can effectively lower circulating tumor DNA levels, promote bone tissue proliferation, inhibit apoptosis, and activate the PI3K/Akt signaling pathway, thereby influencing bone cell function. These findings provide a basis for aspirin's potential application in treating metastatic colorectal cancer and encourage further research on its mechanism and clinical use.

MeSH terms

  • Aged
  • Apoptosis* / drug effects
  • Aspirin* / pharmacology
  • Aspirin* / therapeutic use
  • Bone Density / drug effects
  • Cell Proliferation / drug effects
  • Circulating Tumor DNA* / blood
  • Circulating Tumor DNA* / genetics
  • Colorectal Neoplasms* / drug therapy
  • Colorectal Neoplasms* / genetics
  • Colorectal Neoplasms* / pathology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Osteoblasts / drug effects
  • Osteoblasts / metabolism
  • Osteoblasts / pathology
  • Osteoporosis / drug therapy
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / drug effects

Substances

  • Aspirin
  • Circulating Tumor DNA
  • Proto-Oncogene Proteins c-akt
  • Phosphatidylinositol 3-Kinases