Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Revista Brasileira de Farmacognosia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2017000300324 |
Resumo: | Abstract Glioblastoma is the most common malignant brain tumor representing with poor prognosis, therapy resistance and high metastasis rate. Increased expression and activity of matrix metalloproteinase-2, a member of matrix metalloproteinase family proteins, has been reported in many cancers including glioblastoma. Inhibition of matrix metalloproteinase-2 expression has resulted in reduced aggression of glioblastoma tumors in several reports. In the present study, we evaluated effect of bee venom on expression and activity of matrix metalloproteinase-2 as well as potential toxicity and apoptogenic properties of bee venom on glioblastoma cells. Human A172 glioblastoma cells were treated with increasing concentrations of bee venom. Then, cell viability, apoptosis, matrix metalloproteinase-2 expression, and matrix metalloproteinase-2 activity were measured using MMT assay, propidium iodide staining, real time-PCR, and zymography, respectively. The IC50 value of bee venom was 28.5 µg/ml in which it leads to decrease of cell viability and induction of apoptosis. Incubation with bee venom also decreased the expression of matrix metalloproteinase-2 in this cell line (p < 0.05). In zymography, there was a reverse correlation between bee venom concentration and total matrix metalloproteinase-2 activity. Induction of apoptosis as well as inhibition of matrix metalloproteinase-2 activity and expression can be suggested as molecular mechanisms involved in cytotoxic and antimetastatic effects of bee venom against glioblastoma cells. |
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Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cellsBee venomGlioblastomaMatrix metalloproteinase-2ApoptosisMetastasisZymographyAbstract Glioblastoma is the most common malignant brain tumor representing with poor prognosis, therapy resistance and high metastasis rate. Increased expression and activity of matrix metalloproteinase-2, a member of matrix metalloproteinase family proteins, has been reported in many cancers including glioblastoma. Inhibition of matrix metalloproteinase-2 expression has resulted in reduced aggression of glioblastoma tumors in several reports. In the present study, we evaluated effect of bee venom on expression and activity of matrix metalloproteinase-2 as well as potential toxicity and apoptogenic properties of bee venom on glioblastoma cells. Human A172 glioblastoma cells were treated with increasing concentrations of bee venom. Then, cell viability, apoptosis, matrix metalloproteinase-2 expression, and matrix metalloproteinase-2 activity were measured using MMT assay, propidium iodide staining, real time-PCR, and zymography, respectively. The IC50 value of bee venom was 28.5 µg/ml in which it leads to decrease of cell viability and induction of apoptosis. Incubation with bee venom also decreased the expression of matrix metalloproteinase-2 in this cell line (p < 0.05). In zymography, there was a reverse correlation between bee venom concentration and total matrix metalloproteinase-2 activity. Induction of apoptosis as well as inhibition of matrix metalloproteinase-2 activity and expression can be suggested as molecular mechanisms involved in cytotoxic and antimetastatic effects of bee venom against glioblastoma cells.Sociedade Brasileira de Farmacognosia2017-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2017000300324Revista Brasileira de Farmacognosia v.27 n.3 2017reponame:Revista Brasileira de Farmacognosia (Online)instname:Sociedade Brasileira de Farmacognosia (SBFgnosia)instacron:SBFGNOSIA10.1016/j.bjp.2016.11.006info:eu-repo/semantics/openAccessSisakht,MohsenMashkani,BarataliBazi,AliOstadi,HassanZare,MaryamAvval,Farnaz ZahediSadeghnia,Hamid RezaMojarad,MajidNadri,MohammadGhorbani,AhmadSoukhtanloo,Mohmmadeng2017-06-20T00:00:00Zoai:scielo:S0102-695X2017000300324Revistahttp://www.sbfgnosia.org.br/revista/https://old.scielo.br/oai/scielo-oai.phprbgnosia@ltf.ufpb.br1981-528X0102-695Xopendoar:2017-06-20T00:00Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia)false |
dc.title.none.fl_str_mv |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells |
title |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells |
spellingShingle |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells Sisakht,Mohsen Bee venom Glioblastoma Matrix metalloproteinase-2 Apoptosis Metastasis Zymography |
title_short |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells |
title_full |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells |
title_fullStr |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells |
title_full_unstemmed |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells |
title_sort |
Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells |
author |
Sisakht,Mohsen |
author_facet |
Sisakht,Mohsen Mashkani,Baratali Bazi,Ali Ostadi,Hassan Zare,Maryam Avval,Farnaz Zahedi Sadeghnia,Hamid Reza Mojarad,Majid Nadri,Mohammad Ghorbani,Ahmad Soukhtanloo,Mohmmad |
author_role |
author |
author2 |
Mashkani,Baratali Bazi,Ali Ostadi,Hassan Zare,Maryam Avval,Farnaz Zahedi Sadeghnia,Hamid Reza Mojarad,Majid Nadri,Mohammad Ghorbani,Ahmad Soukhtanloo,Mohmmad |
author2_role |
author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Sisakht,Mohsen Mashkani,Baratali Bazi,Ali Ostadi,Hassan Zare,Maryam Avval,Farnaz Zahedi Sadeghnia,Hamid Reza Mojarad,Majid Nadri,Mohammad Ghorbani,Ahmad Soukhtanloo,Mohmmad |
dc.subject.por.fl_str_mv |
Bee venom Glioblastoma Matrix metalloproteinase-2 Apoptosis Metastasis Zymography |
topic |
Bee venom Glioblastoma Matrix metalloproteinase-2 Apoptosis Metastasis Zymography |
description |
Abstract Glioblastoma is the most common malignant brain tumor representing with poor prognosis, therapy resistance and high metastasis rate. Increased expression and activity of matrix metalloproteinase-2, a member of matrix metalloproteinase family proteins, has been reported in many cancers including glioblastoma. Inhibition of matrix metalloproteinase-2 expression has resulted in reduced aggression of glioblastoma tumors in several reports. In the present study, we evaluated effect of bee venom on expression and activity of matrix metalloproteinase-2 as well as potential toxicity and apoptogenic properties of bee venom on glioblastoma cells. Human A172 glioblastoma cells were treated with increasing concentrations of bee venom. Then, cell viability, apoptosis, matrix metalloproteinase-2 expression, and matrix metalloproteinase-2 activity were measured using MMT assay, propidium iodide staining, real time-PCR, and zymography, respectively. The IC50 value of bee venom was 28.5 µg/ml in which it leads to decrease of cell viability and induction of apoptosis. Incubation with bee venom also decreased the expression of matrix metalloproteinase-2 in this cell line (p < 0.05). In zymography, there was a reverse correlation between bee venom concentration and total matrix metalloproteinase-2 activity. Induction of apoptosis as well as inhibition of matrix metalloproteinase-2 activity and expression can be suggested as molecular mechanisms involved in cytotoxic and antimetastatic effects of bee venom against glioblastoma cells. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-06-01 |
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=S0102-695X2017000300324 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2017000300324 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.bjp.2016.11.006 |
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 |
Sociedade Brasileira de Farmacognosia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Farmacognosia |
dc.source.none.fl_str_mv |
Revista Brasileira de Farmacognosia v.27 n.3 2017 reponame:Revista Brasileira de Farmacognosia (Online) instname:Sociedade Brasileira de Farmacognosia (SBFgnosia) instacron:SBFGNOSIA |
instname_str |
Sociedade Brasileira de Farmacognosia (SBFgnosia) |
instacron_str |
SBFGNOSIA |
institution |
SBFGNOSIA |
reponame_str |
Revista Brasileira de Farmacognosia (Online) |
collection |
Revista Brasileira de Farmacognosia (Online) |
repository.name.fl_str_mv |
Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia) |
repository.mail.fl_str_mv |
rbgnosia@ltf.ufpb.br |
_version_ |
1752122470220955648 |