Anti-cancer effects of DHP107 on canine mammary gland cancer examined through in-vitro and in-vivo mouse xenograft models

被引:0
|
作者
Chae, Hyung-Kyu [1 ,2 ]
Oh, Ye-In [3 ]
Lim, Ga-Hyun [1 ]
Jung, Yun-Chan [4 ]
Park, Seol-Hee [1 ]
An, Ju-Hyun [5 ,6 ]
Park, Su-Min [1 ]
Seo, Kyoung-Won [1 ]
Chu, Sung-Nam [7 ]
Li, Qiang [8 ]
Youn, Hwa-Young [1 ]
机构
[1] Seoul Natl Univ, Coll Vet Med, Lab Vet Internal Med, Seoul 08826, South Korea
[2] Western Referral Anim Med Ctr, Dept Vet Internal Med, Seoul, South Korea
[3] Kyungpook Natl Univ, Coll Vet Med, Dept Vet Internal Med, Daegu, South Korea
[4] CHA Univ, Lab Anim Ctr, CHA Biocomplex, Sungnam, South Korea
[5] Kangwon Natl Univ, Dept Vet Emergency & Crit Care Med, Coll Vet Med, Chuncheon Si, South Korea
[6] Kangwon Natl Univ, Inst Vet Sci, Coll Vet Med, Chunchon, South Korea
[7] DaeHwa Pharmaceut Co Ltd, Pangyo Res Lab, Sungnam, South Korea
[8] YanBian Univ, Agr Coll, Dept Vet Med, Yanji 133000, Jilin, Peoples R China
关键词
Cancer; Chemotherapy; Canine; Oral paclitaxel; Mammary gland cancer; ORAL PACLITAXEL FORMULATION; ADVANCED SOLID TUMORS; BREAST-CANCER; DOGS; CHEMOTHERAPY; EFFICACY; THERAPY;
D O I
10.1186/s12917-023-03837-4
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundCanine mammary gland cancer (CMGC) is a common neoplasm in intact bitches. However, the benefit of adjuvant chemotherapy is unclear. The aim of this study was to investigate the anti-proliferative effects of paclitaxel on CMGC in in-vitro and in-vivo settings.ResultsPaclitaxel dose-dependently inhibited viability and induced G2/M phase cell cycle arrest and apoptosis in both primary and metastatic CMGC cell lines (CIPp and CIPm). In animal experiments, the average tumour volume decreased significantly in proportion to the administered oral paclitaxel dose. By examining tumour tissue using a TUNEL assay and immunohistochemical staining with anti-CD31 as a marker of endothelial differentiation, respectively, it was confirmed that oral paclitaxel induced apoptosis and exerted an anti-angiogenetic effect in tumour tissues. Further, downregulation of cyclin D1 in tumour tissues suggested that oral paclitaxel induced cell cycle arrest in tumour tissues in-vivo.ConclusionsOur results suggest that paclitaxel may have anti-cancer effects on CMGC through cell cycle arrest, induction of apoptosis, and anti-angiogenesis. This study could provide a novel approach to treat CMGC.
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页数:11
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