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dc.contributor.authorGhahhari, NM
dc.contributor.authorGhahhari, HM
dc.contributor.authorKadivar, M
dc.date.accessioned2018-08-26T08:51:17Z
dc.date.available2018-08-26T08:51:17Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/53327
dc.description.abstractBackground: Salivary gland tumors (SGTs) are known for their specific heterogeneity and ambiguous outcome for the affected patients. The LKB1 and SMAD4 genes are pivotal components of important signaling pathways, including AMPK and TGF-?. To our knowledge, no study has reported an association between the expression levels of these genes in SGTs. The expression levels of LKB1 and SMAD4 were evaluated to clarify their possible crosstalk in SGTs. Materials and Methods: A total of 50 fresh tissue specimens were obtained from patients with SGTs, including pleomorphic adenoma (PA), Warthin's tumor (WT), intermediate grade mucoepidermoid carcinoma (MEC), salivary duct carcinoma (SDC), and carcinoma ex pleomorphic adenoma (CexPA), as well as 8 normal samples. Quantitative real-time polymerase chain reaction was performed for all samples with specific primers. Results: Data were analyzed using statistical methods. PA, WT, MEC, and SDC showed a significant decrease in LKB1 levels, but the gene was up-regulated in CexPA. SMAD4 was overexpressed in all samples. Conclusion: The results suggest a possible link between downregulation of LKB1 and overexpression of SMAD4 in SGTs. LKB1 depletion leads to upregulation of SMAD4, promoting epithelial-mesenchymal transition in tumor cells. Therefore, LKB1 and SMAD4 could be key players in inducing tumor heterogeneity in SGTs. é 2012 S. Karger GmbH, Freiburg.
dc.language.isoEnglish
dc.relation.ispartofOnkologie
dc.subjecthydroxymethylglutaryl coenzyme A reductase kinase
dc.subjectprotein kinase LKB1
dc.subjectSmad4 protein
dc.subjecttransforming growth factor beta
dc.subjectadenosquamous carcinoma
dc.subjectarticle
dc.subjectbenign tumor
dc.subjectdata analysis
dc.subjectepithelial mesenchymal transition
dc.subjectgene overexpression
dc.subjecthuman
dc.subjecthuman tissue
dc.subjectintracellular signaling
dc.subjectmajor clinical study
dc.subjectoncogene
dc.subjectpleomorphic adenoma
dc.subjectprotein depletion
dc.subjectquantitative analysis
dc.subjectreal time polymerase chain reaction
dc.subjectreceptor down regulation
dc.subjectreceptor upregulation
dc.subjectsalivary gland carcinoma
dc.subjectsalivary gland tumor
dc.subjectstatistical analysis
dc.subjectstatistical significance
dc.subjecttissue section
dc.subjecttumor cell
dc.subjectWarthin tumor
dc.subjectHumans
dc.subjectProtein Kinases
dc.subjectProtein-Serine-Threonine Kinases
dc.subjectReceptor Cross-Talk
dc.subjectSalivary Gland Neoplasms
dc.subjectSignal Transduction
dc.subjectSmad4 Protein
dc.subjectTissue Distribution
dc.subjectTransforming Growth Factor beta
dc.titleCould a possible crosstalk between ampk and tgf-? signaling pathways be a key player in benign and malignant salivary gland tumors?
dc.typeArticle
dc.citation.volume35
dc.citation.issue12
dc.citation.spage770
dc.citation.epage774
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1159/0003451315


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