Apis meliffera intermissa venom attenuated colitis-associated cancer progression in azoxymethane treated mice

Dahdouh Faouzi1,2, Djeffal Hanane Chainez1, Bourouba Amira1

  • 1Department of Biology, Laboratory of Cell Toxicology, Faculty of Sciences, Badji-Mokhtar, Annaba University, Annaba, BP 23000, Algeria.

PubMed

Insights

Algerian bee venom shows promise in treating colitis-associated colorectal cancer (CAC). This study found bee venom mitigated inflammation and pathological changes in mice, suggesting its potential as an adjunct therapy for CAC.

Area of Science:

  • Immunology and Cancer Research
  • Pharmacology and Toxicology
  • Gastroenterology

Background:

  • Colitis-associated colorectal cancer (CAC) arises from chronic colon inflammation, posing therapeutic challenges.
  • Apis mellifera intermissa venom exhibits anti-inflammatory and anti-tumorigenic properties in preclinical models.
  • Investigating novel therapeutic strategies for CAC is crucial due to its significant morbidity and mortality.

Purpose of the Study:

  • To evaluate the therapeutic potential of Algerian Apis mellifera intermissa venom against azoxymethane (AOM)-induced CAC in mice.
  • To assess the impact of bee venom on hematological parameters, systemic inflammation, and colon histopathology in a CAC model.

Main Methods:

  • Male mice were divided into four groups: control, AOM-induced CAC, bee venom treatment, and combined AOM + bee venom treatment.
  • Colitis-associated colorectal cancer was induced using azoxymethane (AOM) and a high-fat diet.
  • Bee venom was administered intraperitoneally daily for two weeks, with subsequent analysis of body weight, food/water intake, hematology, serum C-reactive protein (CRP), and colon histopathology.

Main Results:

  • AOM induction led to reduced body weight, food/water intake, altered hematological profiles (decreased RBC, HGB, HCT; increased WBC, MCV, MCH), elevated CRP, and severe colon pathology.
  • Co-treatment with bee venom significantly ameliorated these effects, restoring normal hematological values, reducing CRP levels, and improving colon morphology and epithelial integrity.
  • Bee venom treatment alone did not show adverse effects and maintained normal physiological parameters.

Conclusions:

  • Apis mellifera intermissa venom demonstrates significant therapeutic potential in mitigating the progression of colitis-associated colorectal cancer in a mouse model.
  • The venom's anti-inflammatory and protective effects on colon tissue suggest it could be a valuable adjunct therapy for CAC.
  • Further research is warranted to elucidate the specific mechanisms of action and explore clinical applications of bee venom in CAC management.