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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Malandrinos, G. | en |
| dc.contributor.author | Nunes, A. M. | en |
| dc.contributor.author | Zavitsanos, K. | en |
| dc.contributor.author | Hadjiliadis, N. | en |
| dc.date.accessioned | 2015-11-24T16:44:10Z | - |
| dc.date.available | 2015-11-24T16:44:10Z | - |
| dc.identifier.issn | 0033-4545 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/8778 | - |
| dc.rights | Default Licence | - |
| dc.subject | carcinogenesis | en |
| dc.subject | copper(ii) | en |
| dc.subject | histone models | en |
| dc.subject | nickel(ii) | en |
| dc.subject | peptides | en |
| dc.subject | c-terminal tail | en |
| dc.subject | nucleosome core particle | en |
| dc.subject | histone h2a | en |
| dc.subject | ni(ii) ions | en |
| dc.subject | coordination properties | en |
| dc.subject | angstrom resolution | en |
| dc.subject | binding sequence | en |
| dc.subject | oxidative damage | en |
| dc.subject | cu(ii) | en |
| dc.subject | nickel(ii) | en |
| dc.title | Peptide models in the study of the mechanism of carcinogenesis by heavy metals | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | Doi 10.1351/Pac-Con-10-11-14 | - |
| heal.identifier.secondary | <Go to ISI>://000298741900011 | - |
| heal.identifier.secondary | http://pac.iupac.org/publications/pac/pdf/2011/pdf/8309x1751.pdf | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.publicationDate | 2011 | - |
| heal.abstract | The molecular mechanisms of carcinogenesis involving heavy metal ions are not yet fully understood. Histones surrounding DNA are believed to be primary targets for metal ion binding, and such interactions may play a direct or indirect role in metal-induced toxicity carcinogenesis. This paper reviews our results of approximately the last 10 years in this area, starting from small peptide fragments and models of various histones and ending with longer ones. It was found that almost all peptide models reacted strongly with metal ions, and in some cases the peptides in the presense of Cu(II) or Ni(II) were hydrolyzed. Oxidation of deoxyguanosine to 8-oxo-deoxyguanosine under physiological pH values was also observed in the presense of mild oxidation agents like H(2)O(2) and certain metal ion-peptide complexes. With longer peptide chain models, a DNA strand breakage analysis was also carried out, indicating an increased DNA damage by Cu(2+)/H(2)O(2) and Ni(2+)/H(2)O(2) reaction mixtures. The results lead to proposals of possible mechanistic pathways of carcinogenesis caused by Cu(II) and Ni(II). | en |
| heal.publisher | International Union of Pure and Applied Chemistry | en |
| heal.journalName | Pure and Applied Chemistry | en |
| heal.journalType | peer reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Malandrinos-2011-Peptide models in th.pdf | 697 kB | Adobe PDF | View/Open |
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