DNA Adduct Assessment During Antihormonal Treatment of Perianal Gland Tumors With Tamoxifen in Male Dogs

被引:2
|
作者
Brodzki, Adam [1 ]
Tatara, Marcin R. [2 ]
Brodzki, Piotr [3 ]
Balicki, Ireneusz [1 ]
机构
[1] Univ Life Sci Lublin, Fac Vet Med, Dept & Clin Anim Surg, Ul Gleboka 30, PL-20612 Lublin, Poland
[2] Univ Life Sci Lublin, Fac Vet Med, Dept Anim Physiol, Lublin, Poland
[3] Univ Life Sci Lublin, Fac Vet Med, Dept & Clin Anim Reprod, Lublin, Poland
来源
IN VIVO | 2019年 / 33卷 / 03期
关键词
Dog; perianal gland tumors; tamoxifen; DNA adduct; genotoxicity; CHEMICAL CARCINOGENESIS; MOLECULAR DOSIMETRY; DOSE-RESPONSE; EXPOSURE; RAT; INDUCTION; LIVER;
D O I
10.21873/invivo.11532
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: Determination of DNA adduct count was performed in mononuclear cells during antihormonal treatment of perianal gland tumors. Materials and Methods: Eight- to fifteen-year-old dogs with carcinoma (CAR Group; N=5), epithelioma (EPI Group; N=16) or adenoma (ADE Group; N=24) were used. The control group suffered from perineal hernia or rectal diverticulum (CTR Group; N=25). Blood was collected at baseline, and at one and six months after the beginning of the anti-hormonal treatment with tamoxifen (1 mg/kg of body weight). DNA adduct count was determined using autoradiography. Results: At baseline, DNA adduct count reached the highest value in the CTR Group, and the lowest in the EPI Group (p<0.05). Six-month-long therapy with tamoxifen resulted in a significant increase in the DNA adduct count by 78.7%, 221.5% and 198.3% in the ADE, EPI and CAR groups, respectively (p<0.05). Conclusion: Increased DNA adduct formation after long-term administration of tamoxifen shows its genotoxicity.
引用
收藏
页码:731 / 735
页数:5
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