dc.contributor.author |
Kyriazi, M |
en |
dc.contributor.author |
Yova, D |
en |
dc.contributor.author |
Rallis, M |
en |
dc.contributor.author |
Lima, A |
en |
dc.date.accessioned |
2014-03-01T01:23:41Z |
|
dc.date.available |
2014-03-01T01:23:41Z |
|
dc.date.issued |
2006 |
en |
dc.identifier.issn |
0304-3835 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/17089 |
|
dc.subject |
Chemoprevention |
en |
dc.subject |
Hairless mice |
en |
dc.subject |
Pine bark extract |
en |
dc.subject |
Skin carcinogenesis |
en |
dc.subject.classification |
Oncology |
en |
dc.subject.other |
7,12 dimethylbenz[a]anthracene |
en |
dc.subject.other |
dimethylbenz[a]anthracene |
en |
dc.subject.other |
flavonoid |
en |
dc.subject.other |
melanin |
en |
dc.subject.other |
phenol derivative |
en |
dc.subject.other |
pinus maritima extract |
en |
dc.subject.other |
plant extract |
en |
dc.subject.other |
polyphenol |
en |
dc.subject.other |
unclassified drug |
en |
dc.subject.other |
antineoplastic agent |
en |
dc.subject.other |
carcinogen |
en |
dc.subject.other |
animal experiment |
en |
dc.subject.other |
animal model |
en |
dc.subject.other |
antineoplastic activity |
en |
dc.subject.other |
article |
en |
dc.subject.other |
chemoprophylaxis |
en |
dc.subject.other |
controlled study |
en |
dc.subject.other |
drug inhibition |
en |
dc.subject.other |
drug mechanism |
en |
dc.subject.other |
female |
en |
dc.subject.other |
genotoxicity |
en |
dc.subject.other |
male |
en |
dc.subject.other |
melanoma |
en |
dc.subject.other |
mouse |
en |
dc.subject.other |
nonhuman |
en |
dc.subject.other |
papilloma |
en |
dc.subject.other |
pine |
en |
dc.subject.other |
Pinus maritima |
en |
dc.subject.other |
priority journal |
en |
dc.subject.other |
skin carcinogenesis |
en |
dc.subject.other |
skin carcinoma |
en |
dc.subject.other |
ultraviolet radiation |
en |
dc.subject.other |
animal |
en |
dc.subject.other |
bark |
en |
dc.subject.other |
chemically induced disorder |
en |
dc.subject.other |
hairless mouse |
en |
dc.subject.other |
metabolism |
en |
dc.subject.other |
radiation injury |
en |
dc.subject.other |
skin tumor |
en |
dc.subject.other |
time |
en |
dc.subject.other |
Animalia |
en |
dc.subject.other |
Pinus pinaster |
en |
dc.subject.other |
9,10-Dimethyl-1,2-benzanthracene |
en |
dc.subject.other |
Animals |
en |
dc.subject.other |
Anticarcinogenic Agents |
en |
dc.subject.other |
Carcinogens |
en |
dc.subject.other |
Female |
en |
dc.subject.other |
Male |
en |
dc.subject.other |
Melanins |
en |
dc.subject.other |
Mice |
en |
dc.subject.other |
Mice, Inbred HRS |
en |
dc.subject.other |
Neoplasms, Radiation-Induced |
en |
dc.subject.other |
Pinus |
en |
dc.subject.other |
Plant Bark |
en |
dc.subject.other |
Skin Neoplasms |
en |
dc.subject.other |
Time Factors |
en |
dc.subject.other |
Ultraviolet Rays |
en |
dc.title |
Cancer chemopreventive effects of Pinus Maritima bark extract on ultraviolet radiation and ultraviolet radiation-7,12,dimethylbenz(a)anthracene induced skin carcinogenesis of hairless mice |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/j.canlet.2005.06.005 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/j.canlet.2005.06.005 |
en |
heal.language |
English |
en |
heal.publicationDate |
2006 |
en |
heal.abstract |
The bark extract of Pinus Maritima (PBE), a rich in phenolic acids, polyphenols and in particular flavonoids mixture, was examined for skin cancer preventive action that was evaluated in two different experimental animal tumor models induced by ultraviolet radiation (UVR) and combination of UVR with 7,12-dimethylbenz[a]anthracene. Significant decrease in the number of animals bearing tumors and the number of tumors per animal was observed in the PBE treated animals. In the same time significant increase in the viability of these animals was also observed. Furthermore, PBE delayed the appearance of tumors. These results provide strong evidence about the preventive anticancer activity of this extract on non-melanoma skin cancer and its protective effect not only from UVR, but also from more potent carcinogenic agents. (c) 2005 Elsevier Ireland Ltd. All rights reserved. |
en |
heal.publisher |
ELSEVIER IRELAND LTD |
en |
heal.journalName |
Cancer Letters |
en |
dc.identifier.doi |
10.1016/j.canlet.2005.06.005 |
en |
dc.identifier.isi |
ISI:000238563500009 |
en |
dc.identifier.volume |
237 |
en |
dc.identifier.issue |
2 |
en |
dc.identifier.spage |
234 |
en |
dc.identifier.epage |
241 |
en |