Doxorubicin as a Potential Treatment Option in Canine Mammary Tumors

Madalina Luciana Gherman1,2, Oana Zanoaga2, Liviuta Budisan2

  • 1Experimental Center, Iuliu Hatieganu University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.

Veterinary Sciences
|November 24, 2023
PubMed

Insights

Doxorubicin effectively inhibits canine mammary cancer cell proliferation and alters epithelial-to-mesenchymal transition (EMT)-related gene expression in vitro. This study highlights Doxorubicin

Area of Science:

  • Veterinary Oncology
  • Cancer Cell Biology
  • Pharmacology

Background:

  • Canine mammary tumors (CMTs) are a significant health concern in female dogs, necessitating advanced therapeutic strategies beyond surgery.
  • Doxorubicin, a chemotherapy agent, has demonstrated efficacy in human cancers by modulating key cellular processes including apoptosis, autophagy, cell cycle, invasion, and epithelial-to-mesenchymal transition (EMT).

Purpose of the Study:

  • To investigate the effects of Doxorubicin on canine mammary cancer cell lines.
  • To evaluate Doxorubicin's impact on cell proliferation and EMT-related gene expression in canine models.

Main Methods:

  • Treatment of two distinct canine mammary cancer cell lines (P114 and CMT-U27) with Doxorubicin.
  • Assessment of Doxorubicin's effects on cell proliferation rates.
  • Analysis of the expression of genes associated with the epithelial-to-mesenchymal transition (EMT).

Main Results:

  • Doxorubicin treatment significantly inhibited cell proliferation in both P114 and CMT-U27 canine mammary cancer cell lines.
  • Doxorubicin administration led to notable alterations in the expression of EMT-related genes within the studied cell lines.

Conclusions:

  • Doxorubicin demonstrates anti-proliferative effects on canine mammary cancer cells in vitro.
  • The drug influences phenotypic characteristics by altering EMT-related gene expression, suggesting a potential therapeutic role.
  • These findings provide crucial insights into the relationship between Doxorubicin, phenotypic modulation, and proliferation in canine mammary tumor models.

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