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Nitensidine B affects proteins of the glycolytic pathway and induces apoptosis in cervical carcinoma cells immortalized by HPV16

dc.contributor.authorSouza, Felipe de Oliveira [UNESP]
dc.contributor.authorSorbo, Juliana Maria [UNESP]
dc.contributor.authorRegasini, Luis Octavio [UNESP]
dc.contributor.authorBolzani, Vanderlan da Silva [UNESP]
dc.contributor.authorRosa, Jose Cesar
dc.contributor.authorCzernys, Erica da Silva
dc.contributor.authorValente, Valeria [UNESP]
dc.contributor.authorMoreira, Thais Fernanda [UNESP]
dc.contributor.authorNavegante, Geovana [UNESP]
dc.contributor.authorFernandes, Barbara Colatto [UNESP]
dc.contributor.authorSoares, Christiane Pienna [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2018-11-26T17:55:17Z
dc.date.available2018-11-26T17:55:17Z
dc.date.issued2018-09-15
dc.description.abstractBackground: Cervical cancer, the fourth most common type of cancer among women worldwide, accounts for approximately 12% of all types of malignancies that affect women. Natural products have contributed significantly to the development of modern therapies; approximately 70% of the drugs available for chemotherapy are naturally based products. Purpose: The purpose of this study was to examine the biological activities of nitensidine B (NTB), a guanidinic alkaloid isolated from the leaves of Pterogyne nitens Tul. (Fabaceae) in a cervical cancer cell line. Methods: In vitro experiments were performed using cervical carcinoma cells immortalized by human papillomavirus type 16 (HPV16, SiHa cells), since epidemiological and molecular studies have demonstrated robust associations between the etiologies of cervical cancer and HPV infection. Cytotoxicity as well as the effect of NTB treatment on intracellular signals of apoptosis, fragmentation of internucleosomal DNA via terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), and levels of apoptosis effectors (Caspase 3/7) were evaluated. In addition, differential proteomic analysis (iTRAQ) and protein validation using western blot were performed. Results: The cytotoxicity of NTB treatment in the SiHa cell line was concentration-dependent, with the minimum inhibitory concentration of 50% of the cells of 40.98 mu M. In the TUNEL assay, SiHa cell apoptosis with 3/7 caspase activation was reported at 12 h following treatment. Differential proteomic analysis by iTRAQ demonstrated that proteins of the glycolytic pathway, aldolase A, alpha-enolase, pyruvate kinase, and glyceraldehyde 3-phosphate dehydrogenase were underexpressed. Conclusion: These results indicated that NTB could play a role in decreasing glycolysis. Since tumor cells prefer the glycolytic pathway to generate energy, these findings suggest that NTB may be a reliable model for the study of human cervical cancer cell lines immortalized by HPV16, however more experiments can be performed.en
dc.description.affiliationSao Paulo State Univ, Sch Pharmaceut Sci, Dept Clin Anal, Highway Araraquara Jau,Km 01, Araraquara, SP, Brazil
dc.description.affiliationSao Paulo State Univ, Dept Chem & Environm Sci, Inst Biosci Letters & Exact Sci, Cristovao Colombo St 2265, Sao Jose Do Rio Preto, SP, Brazil
dc.description.affiliationSao Paulo State Univ, Inst Chem, Dept Organ Chem, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Ctr Prot Chem, Dept Cellular Mol Biol & Pathogen Bioagents, Fac Med Ribeirao Preto, Ave Bandeirantes 3900, Ribeirao Preto, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Sch Pharmaceut Sci, Dept Clin Anal, Highway Araraquara Jau,Km 01, Araraquara, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Dept Chem & Environm Sci, Inst Biosci Letters & Exact Sci, Cristovao Colombo St 2265, Sao Jose Do Rio Preto, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Inst Chem, Dept Organ Chem, BR-14800900 Araraquara, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipNational Institute of Science and Technology - INCT BioNat
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdNational Institute of Science and Technology - INCT BioNat: 465637/2014-0
dc.description.sponsorshipIdFAPESP: 2014/50926-0
dc.format.extent179-186
dc.identifierhttp://dx.doi.org/10.1016/j.phymed.2018.05.016
dc.identifier.citationPhytomedicine. Jena: Elsevier Gmbh, Urban & Fischer Verlag, v. 48, p. 179-186, 2018.
dc.identifier.doi10.1016/j.phymed.2018.05.016
dc.identifier.fileWOS000443714600020.pdf
dc.identifier.issn0944-7113
dc.identifier.lattes1768025290373669
dc.identifier.orcid0000-0003-1740-7360
dc.identifier.urihttp://hdl.handle.net/11449/164608
dc.identifier.wosWOS:000443714600020
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPhytomedicine
dc.relation.ispartofsjr1,087
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectCervical cancer
dc.subjectNitensidine B
dc.subjectApoptosis
dc.subjectProteomic analysis
dc.subjectGlycolytic pathway
dc.titleNitensidine B affects proteins of the glycolytic pathway and induces apoptosis in cervical carcinoma cells immortalized by HPV16en
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.author.lattes1768025290373669[11]
unesp.author.orcid0000-0002-3705-0971[3]
unesp.author.orcid0000-0003-1740-7360[11]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt
unesp.departmentQuímica e Ciências Ambientais - IBILCEpt
unesp.departmentQuímica Orgânica - IQARpt

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