Anticancer effect of chrysin on canine mammary gland tumor cells via cell cycle arrest and apoptosis

Background: Canine mammary tumors are one of the most common tumors in female dogs, and the development of effective therapeutic agents is a critical clinical challenge.Chrysin, a natural flavonoid compound, has been reported to exhibit anticancer activity in various human cancers through the regulation of cell proliferation and apoptosis.However, the anticancer effects of chrysin on canine mammary tumors have not yet been fully elucidated.Therefore, this study investigated the antiproliferative and apoptosis-inducing effects of chrysin on CMT-U27 cells derived from canine mammary tumors.Methods: Antiproliferative activity was confirmed by treating CMT-U27 cells with chrysin at concentrations of 0-10 µM and evaluating cell viability.Cell proliferation capacity was assessed using Ki-67 immunocytochemistry.The expression levels of cell cycle-related proteins, including CDK2, CDK4, cyclin D, and cyclin E, were analyzed by Western blotting.Additionally, apoptosis-related proteins, including phosphorylated p53 and BCL2, were evaluated to investigate the apoptotic activity of chrysin treatment.Results: Chrysin treatment significantly reduced the viability and migration of CMT-U27 cells and decreased the number of Ki-67-positive cells in a dose-dependent manner.Following chrysin treatment, the expression of CDK2, CDK4, cyclin D, and cyclin E was significantly reduced, indicating that cell cycle progression was inhibited.Additionally, chrysin increased the expression of phosphorylated p53 and decreased BCL2 expression.Conclusions: Chrysin exhibited significant anticancer effects in canine mammary tumor-derived CMT-U27 cells through the inhibition of cell proliferation, accompanied by G2/M phase accumulation and downregulation of cyclin-CDK complex components.In addition, chrysin altered apoptosis-related signaling molecules, including p53 and BCL2.These results suggest that chrysin may have potential as a therapeutic candidate for canine mammary tumors.

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Publication Details

Journal
Journal of Animal Reproduciton and Biotechnology
Published
2026-06-30
DOI
https://doi.org/10.12750/jarb.41.2.58
Primary Topic
Flavonoids in Medical Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Anticancer effect of chrysin on canine mammary gland tumor cells via cell cycle arrest and apoptosis

Jae‐Joong Kim, Hyun-Jung Park, Won-Young Lee, Ran Lee et al.
Journal of Animal Reproduciton and Biotechnology
Flavonoids in Medical Research
article

Anticancer effect of chrysin on canine mammary gland tumor cells via cell cycle arrest and apoptosis

Jae‐Joong Kim, Hyun-Jung Park, Won-Young Lee, Ran Lee, Kwang‐Hyun Cho, Eun-Jung Kim, Hyeon Woo Sim
article en

Abstract

Background: Canine mammary tumors are one of the most common tumors in female dogs, and the development of effective therapeutic agents is a critical clinical challenge.Chrysin, a natural flavonoid compound, has been reported to exhibit anticancer activity in various human cancers through the regulation of cell proliferation and apoptosis.However, the anticancer effects of chrysin on canine mammary tumors have not yet been fully elucidated.Therefore, this study investigated the antiproliferative and apoptosis-inducing effects of chrysin on CMT-U27 cells derived from canine mammary tumors.Methods: Antiproliferative activity was confirmed by treating CMT-U27 cells with chrysin at concentrations of 0-10 µM and evaluating cell viability.Cell proliferation capacity was assessed using Ki-67 immunocytochemistry.The expression levels of cell cycle-related proteins, including CDK2, CDK4, cyclin D, and cyclin E, were analyzed by Western blotting.Additionally, apoptosis-related proteins, including phosphorylated p53 and BCL2, were evaluated to investigate the apoptotic activity of chrysin treatment.Results: Chrysin treatment significantly reduced the viability and migration of CMT-U27 cells and decreased the number of Ki-67-positive cells in a dose-dependent manner.Following chrysin treatment, the expression of CDK2, CDK4, cyclin D, and cyclin E was significantly reduced, indicating that cell cycle progression was inhibited.Additionally, chrysin increased the expression of phosphorylated p53 and decreased BCL2 expression.Conclusions: Chrysin exhibited significant anticancer effects in canine mammary tumor-derived CMT-U27 cells through the inhibition of cell proliferation, accompanied by G2/M phase accumulation and downregulation of cyclin-CDK complex components.In addition, chrysin altered apoptosis-related signaling molecules, including p53 and BCL2.These results suggest that chrysin may have potential as a therapeutic candidate for canine mammary tumors.

Journal of Animal Reproduciton and BiotechnologyVol. 41(2)
Konkuk University (KR), Sangji University (KR)
Sangji University
Good health and well-being
Openalex Percentile: Top 9%
Flavonoids in Medical Research
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