Myricetin induces pancreatic cancer cell death via the induction of apoptosis and inhibition of the phosphatidylinositol 3-kinase (PI3K) signaling pathway

被引:170
作者
Phillips, P. A. [1 ]
Sangwan, V. [1 ]
Borja-Cacho, D. [1 ]
Dudeja, V. [1 ]
Vickers, S. M. [1 ]
Saluja, A. K. [1 ]
机构
[1] Univ Minnesota, Dept Surg, Minneapolis, MN 55455 USA
关键词
Pancreatic cancer; Myricetin; Orthotopic model; Apoptosis; CYTOCHROME-C RELEASE; DIETARY FLAVONOIDS; IN-VITRO; GROWTH; PROLIFERATION; CYTOTOXICITY; MANIPULATION; WORTMANNIN; MIGRATION; LY294002;
D O I
10.1016/j.canlet.2011.05.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Pancreatic cancer is the fourth leading cause of cancer related deaths and is a disease with poor prognosis. It is refractory to standard chemotherapeutic drugs or to novel treatment modalities, making it imperative to find new treatments. In this study, using both primary and metastatic pancreatic cancer cell lines, we have demonstrated that the flavonoid myricetin induced pancreatic cancer cell death in vitro via apoptosis, and caused a decrease in PI3 kinase activity. In vivo, treatment of orthotopic pancreatic tumors with myricetin resulted in tumor regression and decreased metastatic spread. Importantly, myricetin was non-toxic, both in vitro and in vivo, underscoring its use as a therapeutic agent against pancreatic cancer. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:181 / 188
页数:8
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