Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study
Autor(a) principal: | |
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Data de Publicação: | 2002 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Dental Journal |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402002000200006 |
Resumo: | Low level laser therapy (LLLT) has been used successfully in biomedicine and some of the results are thought to be related to cell proliferation. The effects of LLLT on cell proliferation is debatable because studies have found both an increase and a decrease in proliferation of cell cultures. Cell culture is an excellent method to assess both effects and dose of treatment. The aim of this study was to assess the effect of 635nm and 670nm laser irradiation of H.Ep.2 cells in vitro using MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide). The cells were obtained from squamous cell carcinoma (SCC) of the larynx and were routinely processed from defrost to the experimental condition. Twenty-four hours after transplantation the cells were irradiated with doses ranging from 0.04 to 0.48J/cm² for seven consecutive days (5 mW diode lasers: 635nm or 670nm, beam cross-section ~1mm) at local light doses between 0.04 and 0.48J/cm². The results showed that 635nm laser light did not significantly stimulate the proliferation of H.Ep.2 cells at doses of 0.04J/cm² to 0.48J/cm², However, 670nm laser irradiation led to an increased cell proliferation when compared to both control and 635nm irradiated cells. The best cell proliferation was found with 670nm laser irradiated cultures exposed to doses of doses of 0.04 to 0.48J/cm². We conclude that both dose and wavelength are factors that may affect cell proliferation of H.Ep.2 cells. |
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Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" studycell proliferationhazardsstimulatory effectLow level laser therapy (LLLT) has been used successfully in biomedicine and some of the results are thought to be related to cell proliferation. The effects of LLLT on cell proliferation is debatable because studies have found both an increase and a decrease in proliferation of cell cultures. Cell culture is an excellent method to assess both effects and dose of treatment. The aim of this study was to assess the effect of 635nm and 670nm laser irradiation of H.Ep.2 cells in vitro using MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide). The cells were obtained from squamous cell carcinoma (SCC) of the larynx and were routinely processed from defrost to the experimental condition. Twenty-four hours after transplantation the cells were irradiated with doses ranging from 0.04 to 0.48J/cm² for seven consecutive days (5 mW diode lasers: 635nm or 670nm, beam cross-section ~1mm) at local light doses between 0.04 and 0.48J/cm². The results showed that 635nm laser light did not significantly stimulate the proliferation of H.Ep.2 cells at doses of 0.04J/cm² to 0.48J/cm², However, 670nm laser irradiation led to an increased cell proliferation when compared to both control and 635nm irradiated cells. The best cell proliferation was found with 670nm laser irradiated cultures exposed to doses of doses of 0.04 to 0.48J/cm². We conclude that both dose and wavelength are factors that may affect cell proliferation of H.Ep.2 cells.Fundação Odontológica de Ribeirão Preto2002-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402002000200006Brazilian Dental Journal v.13 n.2 2002reponame:Brazilian Dental Journalinstname:Fundação Odontológica de Ribeirão Preto (FUNORP)instacron:FUNORP10.1590/S0103-64402002000200006info:eu-repo/semantics/openAccessPinheiro,Antonio Luiz BarbosaNascimento,Silene Carneiro doVieira,Alessandro Leonardo de BarrosRolim,Aluízio BarrosSilva,Pedro Soriano daBrugnera Jr.,Aldoeng2003-04-04T00:00:00Zoai:scielo:S0103-64402002000200006Revistahttps://www.scielo.br/j/bdj/https://old.scielo.br/oai/scielo-oai.phpbdj@forp.usp.br||sergio@fosjc.unesp.br1806-47600103-6440opendoar:2003-04-04T00:00Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)false |
dc.title.none.fl_str_mv |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study |
title |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study |
spellingShingle |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study Pinheiro,Antonio Luiz Barbosa cell proliferation hazards stimulatory effect |
title_short |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study |
title_full |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study |
title_fullStr |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study |
title_full_unstemmed |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study |
title_sort |
Does LLLT stimulate laryngeal carcinoma cells? An "in vitro" study |
author |
Pinheiro,Antonio Luiz Barbosa |
author_facet |
Pinheiro,Antonio Luiz Barbosa Nascimento,Silene Carneiro do Vieira,Alessandro Leonardo de Barros Rolim,Aluízio Barros Silva,Pedro Soriano da Brugnera Jr.,Aldo |
author_role |
author |
author2 |
Nascimento,Silene Carneiro do Vieira,Alessandro Leonardo de Barros Rolim,Aluízio Barros Silva,Pedro Soriano da Brugnera Jr.,Aldo |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Pinheiro,Antonio Luiz Barbosa Nascimento,Silene Carneiro do Vieira,Alessandro Leonardo de Barros Rolim,Aluízio Barros Silva,Pedro Soriano da Brugnera Jr.,Aldo |
dc.subject.por.fl_str_mv |
cell proliferation hazards stimulatory effect |
topic |
cell proliferation hazards stimulatory effect |
description |
Low level laser therapy (LLLT) has been used successfully in biomedicine and some of the results are thought to be related to cell proliferation. The effects of LLLT on cell proliferation is debatable because studies have found both an increase and a decrease in proliferation of cell cultures. Cell culture is an excellent method to assess both effects and dose of treatment. The aim of this study was to assess the effect of 635nm and 670nm laser irradiation of H.Ep.2 cells in vitro using MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide). The cells were obtained from squamous cell carcinoma (SCC) of the larynx and were routinely processed from defrost to the experimental condition. Twenty-four hours after transplantation the cells were irradiated with doses ranging from 0.04 to 0.48J/cm² for seven consecutive days (5 mW diode lasers: 635nm or 670nm, beam cross-section ~1mm) at local light doses between 0.04 and 0.48J/cm². The results showed that 635nm laser light did not significantly stimulate the proliferation of H.Ep.2 cells at doses of 0.04J/cm² to 0.48J/cm², However, 670nm laser irradiation led to an increased cell proliferation when compared to both control and 635nm irradiated cells. The best cell proliferation was found with 670nm laser irradiated cultures exposed to doses of doses of 0.04 to 0.48J/cm². We conclude that both dose and wavelength are factors that may affect cell proliferation of H.Ep.2 cells. |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402002000200006 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402002000200006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-64402002000200006 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Fundação Odontológica de Ribeirão Preto |
publisher.none.fl_str_mv |
Fundação Odontológica de Ribeirão Preto |
dc.source.none.fl_str_mv |
Brazilian Dental Journal v.13 n.2 2002 reponame:Brazilian Dental Journal instname:Fundação Odontológica de Ribeirão Preto (FUNORP) instacron:FUNORP |
instname_str |
Fundação Odontológica de Ribeirão Preto (FUNORP) |
instacron_str |
FUNORP |
institution |
FUNORP |
reponame_str |
Brazilian Dental Journal |
collection |
Brazilian Dental Journal |
repository.name.fl_str_mv |
Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP) |
repository.mail.fl_str_mv |
bdj@forp.usp.br||sergio@fosjc.unesp.br |
_version_ |
1754204089629016064 |