Anticancer activity of Turkish marine extracts: a purple sponge extract induces apoptosis with multitarget kinase inhibition activity.
Animals
Antineoplastic Agents
/ pharmacology
Apoptosis
/ drug effects
Biological Products
/ pharmacology
Cell Line, Tumor
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Humans
Neoplasms
/ drug therapy
Porifera
Protein Kinase Inhibitors
/ pharmacology
Receptor, Platelet-Derived Growth Factor beta
/ antagonists & inhibitors
Turkey
Vascular Endothelial Growth Factor Receptor-2
/ antagonists & inhibitors
Apoptosis
Cancer
Marine products
Tyrosine kinase inhibitors
Journal
Investigational new drugs
ISSN: 1573-0646
Titre abrégé: Invest New Drugs
Pays: United States
ID NLM: 8309330
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
06
01
2020
accepted:
10
02
2020
pubmed:
18
2
2020
medline:
15
9
2021
entrez:
17
2
2020
Statut:
ppublish
Résumé
Marine natural products have drawn a great deal of attention as a vital source of new drugs for the last five decades. However, marine organisms in the seas surrounding Turkey (the Black Sea, the Aegean Sea and the Mediterranean Sea) haven't been yet extensively explored. In the present study, three marine organisms (Dysidea avara, Microcosmus sabatieri and Echinaster sepositus) were sampled from the Dardanelles (Turkish Straits System, Western Turkey) by scientific divers, transferred to the laboratory and then were extracted with 70% ethanol. The extracts were tested for their cytotoxic effect against K562, KMS-12PE, A549, and A375 cancer cell lines. The sponge extract elicited the most promising cytotoxic activity, thus it was further evaluated against H929, MCF-7, HeLa, and HCT116 cancer cells. Most of the designated cells showed a considerable sensitivity for the sponge extract particularly H929, K562, KMS-12PE and HeLa cells with IC
Identifiants
pubmed: 32062733
doi: 10.1007/s10637-020-00911-8
pii: 10.1007/s10637-020-00911-8
doi:
Substances chimiques
Antineoplastic Agents
0
Biological Products
0
Protein Kinase Inhibitors
0
KDR protein, human
EC 2.7.10.1
PDGFRB protein, human
EC 2.7.10.1
Receptor, Platelet-Derived Growth Factor beta
EC 2.7.10.1
Vascular Endothelial Growth Factor Receptor-2
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1326-1333Références
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