Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy

BACKGROUND: Photodynamic therapy is an alternative treatment of muco-cutaneous tumors that uses a light source able to photoactivate a chemical compound that acts as a photosensitizer. The phthalocyanines append to a wide chemical class that encompasses a large range of compounds; out of them alumin...

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Autores principales: Matei,Clara, Tampa,Mircea, Caruntu,Constantin, Ion,Rodica-Mariana, Georgescu,Simona-Roxana, Dumitrascu,Georgiana Roxana, Constantin,Carolina, Neagu,Monica
Lenguaje:English
Publicado: Sociedad de Biología de Chile 2014
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602014000100033
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spelling oai:scielo:S0716-976020140001000332015-10-30Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapyMatei,ClaraTampa,MirceaCaruntu,ConstantinIon,Rodica-MarianaGeorgescu,Simona-RoxanaDumitrascu,Georgiana RoxanaConstantin,CarolinaNeagu,Monica Aluminum di-sulphonated phthalocyanine DOK cells Photodynamic therapy Protein microarray BACKGROUND: Photodynamic therapy is an alternative treatment of muco-cutaneous tumors that uses a light source able to photoactivate a chemical compound that acts as a photosensitizer. The phthalocyanines append to a wide chemical class that encompasses a large range of compounds; out of them aluminium-substituted disulphonated phthalocyanine possesses a good photosensitizing potential. RESULTS: The destructive effects of PDT with aluminium-substituted disulphonated phthalocyanine are achieved by induction of apoptosis in tumoral cells as assessed by flow cytometry analysis. Using protein microarray we evaluate the possible molecular pathways by which photodynamic therapy activates apoptosis in dysplastic oral keratinocytes cells, leading to the tumoral cells destruction. Among assessed analytes, Bcl-2, P70S6K kinase, Raf-1 and Bad proteins represent the apoptosis related biomolecules that showed expression variations with the greatest amplitude. CONCLUSIONS: Up to date, the intimate molecular apoptotic mechanisms activated by photodynamic therapy with this type of phthalocyanine in dysplastic human oral keratinocytes are not completely elucidated. With protein microarray as high-throughput proteomic approach a better understanding of the manner in which photodynamic therapy leads to tumoral cell destruction can be obtained, by depicting apoptotic molecules that can be potentially triggered in future anti-tumoral therapies.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.47 20142014-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602014000100033en10.1186/0717-6287-47-33
institution Scielo Chile
collection Scielo Chile
language English
topic Aluminum di-sulphonated phthalocyanine
DOK cells
Photodynamic therapy
Protein microarray
spellingShingle Aluminum di-sulphonated phthalocyanine
DOK cells
Photodynamic therapy
Protein microarray
Matei,Clara
Tampa,Mircea
Caruntu,Constantin
Ion,Rodica-Mariana
Georgescu,Simona-Roxana
Dumitrascu,Georgiana Roxana
Constantin,Carolina
Neagu,Monica
Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy
description BACKGROUND: Photodynamic therapy is an alternative treatment of muco-cutaneous tumors that uses a light source able to photoactivate a chemical compound that acts as a photosensitizer. The phthalocyanines append to a wide chemical class that encompasses a large range of compounds; out of them aluminium-substituted disulphonated phthalocyanine possesses a good photosensitizing potential. RESULTS: The destructive effects of PDT with aluminium-substituted disulphonated phthalocyanine are achieved by induction of apoptosis in tumoral cells as assessed by flow cytometry analysis. Using protein microarray we evaluate the possible molecular pathways by which photodynamic therapy activates apoptosis in dysplastic oral keratinocytes cells, leading to the tumoral cells destruction. Among assessed analytes, Bcl-2, P70S6K kinase, Raf-1 and Bad proteins represent the apoptosis related biomolecules that showed expression variations with the greatest amplitude. CONCLUSIONS: Up to date, the intimate molecular apoptotic mechanisms activated by photodynamic therapy with this type of phthalocyanine in dysplastic human oral keratinocytes are not completely elucidated. With protein microarray as high-throughput proteomic approach a better understanding of the manner in which photodynamic therapy leads to tumoral cell destruction can be obtained, by depicting apoptotic molecules that can be potentially triggered in future anti-tumoral therapies.
author Matei,Clara
Tampa,Mircea
Caruntu,Constantin
Ion,Rodica-Mariana
Georgescu,Simona-Roxana
Dumitrascu,Georgiana Roxana
Constantin,Carolina
Neagu,Monica
author_facet Matei,Clara
Tampa,Mircea
Caruntu,Constantin
Ion,Rodica-Mariana
Georgescu,Simona-Roxana
Dumitrascu,Georgiana Roxana
Constantin,Carolina
Neagu,Monica
author_sort Matei,Clara
title Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy
title_short Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy
title_full Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy
title_fullStr Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy
title_full_unstemmed Protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy
title_sort protein microarray for complex apoptosis monitoring of dysplastic oral keratinocytes in experimental photodynamic therapy
publisher Sociedad de Biología de Chile
publishDate 2014
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602014000100033
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