Auranofin Suppresses the Growth of Canine Mammary Tumour Cells and Induces Apoptosis via the PI3K/AKT Pathway

被引:1
作者
Lin, Zhaoyan [1 ,2 ]
Chen, Rong [1 ,2 ]
Wang, Jiao [1 ,2 ]
Zheng, Yu [1 ,2 ]
He, Zixuan [1 ,2 ]
Yan, Ye [1 ,2 ]
Zhang, Linxi [1 ]
Huang, Xiaohong [1 ,2 ]
Zhang, Hong [3 ]
机构
[1] Fujian Agr & Forestry Univ, Coll Anim Sci, Fuzhou, Peoples R China
[2] Fujian Agr & Forestry Univ, Fujian Key Lab Tradit Chinese Vet Med & Anim Hlth, Fuzhou 350002, Peoples R China
[3] Anhui Agr Univ, Coll Anim Sci & Technol, Hefei, Peoples R China
基金
中国国家自然科学基金;
关键词
3D cell culture; apoptosis; auranofin; CMT; PI3K/AKT; ANTICANCER ACTIVITY; CANCER; ESTABLISHMENT; INHIBITION; COMPOUND; MODELS; LINES;
D O I
10.1111/vco.13005
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Canine mammary gland tumour (CMT) is the most common spontaneous tumour in intact female dogs and often exhibits metastases. Auranofin (AF) is a gold complex used for treating rheumatism. The excellent anti-tumour ability of AF has been demonstrated in various types of human and canine tumours. In this study, five CMT cell lines (CIPp, CMT-7364, CHMp, CIPm and CTBp) and three CMT primary cells (G7894, L1883 and L6783) were used to explore the anti-tumour effect of AF on CMT. Two CMT cell lines (CIPp and CMT-7364) were used to search the underlying mechanism of the effect of AF on CMT. The results showed that AF inhibited the growth, migration, invasion, and colony formation abilities of CMT cells. Additionally, the growth of CMT in a 3D cell culture model was effectively suppressed by AF. Furthermore, AF induced cell apoptosis of CMT cells via the PI3K/AKT pathway. In conclusion, AF effectively induces CMT apoptosis by regulating the PI3K/AKT pathway, indicating that AF should be explored as a potential CMT treatment in future studies.
引用
收藏
页码:555 / 565
页数:11
相关论文
共 41 条
[21]   Auranofin-mediated inhibition of PI3K/AKT/mTOR axis and anticancer activity in non-small cell lung cancer cells [J].
Li, Hongyu ;
Hu, Jing ;
Wu, Shuhong ;
Wang, Li ;
Cao, Xiaobo ;
Zhang, Xiaoshan ;
Dai, Bingbing ;
Cao, Mengru ;
Shao, Ruping ;
Zhang, Ran ;
Majidi, Mourad ;
Ji, Lin ;
Heymach, John V. ;
Wang, Michael ;
Pan, Shiyang ;
Minna, John ;
Mehran, Reza J. ;
Swisher, Stephen G. ;
Roth, Jack A. ;
Fang, Bingliang .
ONCOTARGET, 2016, 7 (03) :3548-3558
[22]   Targeting the PI3K/AKT/mTOR and RAF/MEK/ERK pathways for cancer therapy [J].
Li, Qingfang ;
Li, Zhihui ;
Luo, Ting ;
Shi, Huashan .
MOLECULAR BIOMEDICINE, 2022, 3 (01)
[23]   Auranofin and ICG-001 Emerge Synergistic Anti-tumor Effect on Canine Breast Cancer by Inducing Apoptosis via Mitochondrial Pathway [J].
Lin, Zhaoyan ;
Lin, Zixiang ;
Zhao, Ying ;
Cheng, Nan ;
Zhang, Di ;
Lin, Jiahao ;
Zhang, Hong ;
Lin, Degui .
FRONTIERS IN VETERINARY SCIENCE, 2021, 8
[24]   Combination of Auranofin and ICG-001 Suppress the Proliferation and Metastasis of Colon Cancer [J].
Lin, Zhaoyan ;
Li, Qingqing ;
Zhao, Ying ;
Lin, Zixiang ;
Cheng, Nan ;
Zhang, Di ;
Liu, Gang ;
Lin, Jiahao ;
Zhang, Hong ;
Lin, Degui .
FRONTIERS IN ONCOLOGY, 2021, 11
[25]   Next Generation Gold Drugs and Probes: Chemistry and Biomedical Applications [J].
Mertens, R. Tyler ;
Gukathasan, Sailajah ;
Arojojoye, Adedamola S. ;
Olelewe, Chibuzor ;
Awuah, Samuel G. .
CHEMICAL REVIEWS, 2023, 123 (10) :6612-6667
[26]   Understanding of tumourigenesis in canine mammary tumours based on cancer stem cell research [J].
Michishita, Masaki .
VETERINARY JOURNAL, 2020, 265
[27]   Cyclopedic protein expression analysis of cultured canine mammary gland adenocarcinoma cells from six tumours [J].
Nakagawa, T ;
Watanabe, M ;
Ohashi, E ;
Uyama, R ;
Takauji, S ;
Mochizuki, M ;
Nishimura, R ;
Ogawa, H ;
Sugano, S ;
Sasaki, N .
RESEARCH IN VETERINARY SCIENCE, 2006, 80 (03) :317-323
[28]   3D cell-based biosensor for cell viability and drug assessment by 3D electric cell/matrigel-substrate impedance sensing [J].
Pan, Yuxiang ;
Hu, Ning ;
Wei, Xinwei ;
Gong, Lin ;
Zhang, Bin ;
Wan, Hao ;
Wang, Ping .
BIOSENSORS & BIOELECTRONICS, 2019, 130 :344-351
[29]   Auranofin displays anticancer activity against ovarian cancer cells through FOXO3 activation independent of p53 [J].
Park, See-Hyoung ;
Lee, Jung Han ;
Berek, Jonathan S. ;
Hu, Mickey C. -T. .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2014, 45 (04) :1691-1698
[30]   Comparative oncology approach to drug repurposing in osteosarcoma [J].
Parrales, Alejandro ;
McDonald, Peter ;
Ottomeyer, Megan ;
Roy, Anuradha ;
Shoenen, Frank J. ;
Broward, Melinda ;
Bruns, Tyce ;
Themm, Douglas H. ;
Weir, Scott J. ;
Neville, Kathleen A. ;
Iwakuma, Tomoo ;
Fulbright, Joy M. .
PLOS ONE, 2018, 13 (03)