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Neuromedin B receptor antagonist suppresses tumor angiogenesis and tumor growth in vitro and in vivo
被引:23
|作者:
Park, Hyun-Joo
Kim, Su-Ryun
Kim, Mi-Kyoung
Choi, Kyu-Sil
[2
]
Jang, Hye-Ock
Yun, Il
Bae, Soo-Kyung
Bae, Moon-Kyoung
[1
]
机构:
[1] Pusan Natl Univ, Sch Dent, Dept Oral Physiol, Yangsan 626870, South Korea
[2] Sungkyunkwan Univ, Mol & Cellular Imaging Ctr, Samsung Biomed Res Inst, Sch Med, Seoul 136710, South Korea
关键词:
Neuromedin B receptor antagonist;
Vascular endothelial cells;
Angiogenesis;
Breast cancer cells;
Tumor growth;
GASTRIN-RELEASING-PEPTIDE;
BOMBESIN-LIKE PEPTIDES;
ACTIVATED PROTEIN-KINASE;
CANCER CELL-LINES;
HUMAN BREAST;
SIGNAL-TRANSDUCTION;
EPITHELIAL-CELLS;
GENE-EXPRESSION;
DISEASE STATES;
PROLIFERATION;
D O I:
10.1016/j.canlet.2011.08.014
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Neuromedin B (NMB), a member of the mammalian bombesin-like peptide family, and its receptor were aberrantly expressed in vascularized solid tumors. Here, the NMB receptor (NMB-R) antagonist PD168368 specifically inhibited both NMB-induced in vivo and in vitro angiogenesis. In addition, PD168368 showed growth inhibitory effects on MDA-MB-231 breast cancer cells by inducing cell cycle arrest and apoptosis. Furthermore, PD168368 effectively suppressed tumor growth in a xenograft model of breast tumor in vivo. Overall, NMB-R antagonist exhibited a significant antitumor activity by simultaneously inhibiting neovascularization and cancer cell growth, thereby suggesting that NMB-R could be a potential therapeutic target for cancer treatment. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
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页码:117 / 127
页数:11
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