Back to Search Start Over

Frondoside A from sea cucumber and nymphaeols from Okinawa propolis: Natural anti-cancer agents that selectively inhibit PAK1 in vitro.

Authors :
Nguyen BCQ
Yoshimura K
Kumazawa S
Tawata S
Maruta H
Source :
Drug discoveries & therapeutics [Drug Discov Ther] 2017 May 30; Vol. 11 (2), pp. 110-114. Date of Electronic Publication: 2017 Apr 24.
Publication Year :
2017

Abstract

A sulfated saponin called "Frondoside A" (FRA) from sea cucumber and ingredients from Okinawa propolis (OP) have been previously shown to suppress the PAK1-dependent growth of A549 lung cancer as well as pancreatic cancer cells. However, the precise molecular mechanism underlying their anti-cancer action still remains to be clarified. In this study, for the first time, we found that both FRA and OP directly inhibit PAK1 in vitro in a selective manner (far more effectively than two other oncogenic kinases, LIMK and AKT). Furthermore, at least two major anti-cancer ingredients of OP, nymphaeols A and C, also directly inhibit PAK1 in vitro in a selective manner. To the best of our knowledge, FRA is the first marine compound that selectively inhibits PAK1. Likewise, these nymphaeols are the first propolis ingredients that selectively inhibit PAK1.

Details

Language :
English
ISSN :
1881-7831
Volume :
11
Issue :
2
Database :
MEDLINE
Journal :
Drug discoveries & therapeutics
Publication Type :
Academic Journal
Accession number :
28442678
Full Text :
https://doi.org/10.5582/ddt.2017.01011