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Frondoside A from sea cucumber and nymphaeols from Okinawa propolis: Natural anti-cancer agents that selectively inhibit PAK1 in vitro.
- 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.
- Subjects :
- A549 Cells
Animals
Chromatography, High Pressure Liquid
Flavanones chemistry
Flavanones pharmacology
Flavonoids chemistry
Flavonoids pharmacology
Glycosides chemistry
Humans
In Vitro Techniques
Lim Kinases antagonists & inhibitors
Lim Kinases drug effects
Propolis chemistry
Proto-Oncogene Proteins c-akt antagonists & inhibitors
Proto-Oncogene Proteins c-akt drug effects
Sea Cucumbers
Triterpenes chemistry
p21-Activated Kinases antagonists & inhibitors
Antineoplastic Agents pharmacology
Glycosides pharmacology
Propolis pharmacology
Triterpenes pharmacology
p21-Activated Kinases drug effects
Subjects
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