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-blockers inhibit the viability of breast cancer cells by regulating the ERK/COX-2 signaling pathway and the drug response is affected by ADRB2 single-nucleotide polymorphisms

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成果类型:
期刊论文
作者:
Xie, Wan-Ying;He, Ruo-Hui;Zhang, Jun;He, Yi-Jing;Wan, Zan;...
通讯作者:
Liu, Jie
作者机构:
[Xie, Wan-Ying; Liu, Jie; Mcleod, Howard L.; He, Ruo-Hui; Li, Zhi; Tang, Yong-Jun; Wan, Zan; He, Yi-Jing; Zhou, Cheng-Fang] Cent S Univ, Xiangya Hosp, Dept Clin Pharmacol, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China.
[Xie, Wan-Ying; Liu, Jie; He, Ruo-Hui; Li, Zhi; Wan, Zan; He, Yi-Jing; Zhou, Cheng-Fang] Cent S Univ, Inst Clin Pharmacol, Hunan Key Lab Pharmacogenet, Changsha 410078, Hunan, Peoples R China.
[Liu, Jie; He, Ruo-Hui; Li, Zhi; He, Yi-Jing] Univ South China, Cooperat Innovat Ctr Mol Target New Drug Study, Hengyang 421001, Hunan, Peoples R China.
[Zhang, Jun] Cent S Univ, Xiangya Hosp, Dept Nephrol, Changsha 410008, Hunan, Peoples R China.
[Tang, Yong-Jun] Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China.
通讯机构:
[Liu, Jie] C
Cent S Univ, Xiangya Hosp, Dept Clin Pharmacol, 110 Xiangya Rd, Changsha 410008, Hunan, Peoples R China.
语种:
英文
关键词:
triple-negative breast cancer;-blocker;-adrenergic receptor;mitogen-activated protein kinase signaling pathway;(2)-adrenergic receptor single-nucleotide polymorphisms
期刊:
ONCOLOGY REPORTS
ISSN:
1021-335X
年:
2019
卷:
41
期:
1
页码:
341-350
基金类别:
National Natural Science Foundation of China [81070902]; Young Scientists Fund of the National Natural Science Foundation of China [30600774]; China Postdoctoral Science Foundation [201104515, 2012M510138]
机构署名:
本校为其他机构
院系归属:
药学与生物科学学院
摘要:
The (2)-adrenergic receptor ((2)-AR, encoded by the ADRB2 gene) is a member of the G-protein-coupled receptor superfamily that can be stimulated by catecholamines. Studies in vivo and in vitro have confirmed that -blockers (-AR antagonists) exert antitumor effects on various tumors. Furthermore, ADRB2 single-nucleotide polymorphisms (SNPs) have been identified to alter the expression and conformation of (2)-AR, which may alter the -blocker drug response. The aim of the present study was to investigate the effect of -blockers on triple-negative breast cancer cells and determine whether ADRB2 SN...

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