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Brazilian Propolis Suppresses Angiogenesis by Inducing Apoptosis in Tube‐Forming Endothelial Cells through Inactivation of Survival Signal ERK1/2
Author(s) -
Kazuhiro Kunimasa,
MokRyeon Ahn,
Tomomi Kobayashi,
Ryoji Eguchi,
Shigenori Kumazawa,
Yoshihiro Fujimori,
Takashi Nakano,
Tsutomu Nakayama,
Kazuhiko Kaji,
Toshiro Ohta
Publication year - 2009
Publication title -
evidence-based complementary and alternative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.552
H-Index - 90
eISSN - 1741-4288
pISSN - 1741-427X
DOI - 10.1093/ecam/nep024
Subject(s) - propolis , angiogenesis , protein kinase b , apoptosis , poly adp ribose polymerase , mapk/erk pathway , chemistry , microbiology and biotechnology , signal transduction , kinase , blot , phosphorylation , extracellular , biology , cancer research , biochemistry , dna , polymerase , food science , gene
We recently reported that propolis suppresses tumor-induced angiogenesis through tube formation inhibition and apoptosis induction in endothelial cells. However, molecular mechanisms underlying such angiogenesis suppression by propolis have not been fully elucidated. The aim of this study was to investigate the effects of ethanol extract of Brazilian propolis (EEBP) on two major survival signals, extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt, and to elucidate whether changes in these signals were actually involved in antiangiogenic effects of the propolis. Detection by western blotting revealed that EEBP suppressed phosphorylation of ERK1/2, but not that of Akt. Pharmacological inhibition by U0126 demonstrated that ERK1/2 inactivation alone was enough to inhibit tube formation and induce apoptosis. It was also shown that EEBP and U0126 similarly induced activation of caspase-3 and cleavage of poly ADP-ribose polymerase (PARP) and lamin A/C, all of which are molecular markers of apoptosis. These results indicate that inhibition of survival signal ERK1/2, and subsequent induction of apoptosis, is a critical mechanism of angiogenesis suppression by EEBP.

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