Correlation between the DNA methylation and gene expression of IGFBP5 in breast cancer

MakaleAçık ErişimScopus SJRQ3

Özet

BACKGROUND: The insulin-like growth factor binding protein5 (IGFBP5) is often dysregulated in human cancers and considered neither a tumor suppressor nor an oncogene. OBJECTIVE: We aim to examine the reason of the changeable gene regulation of IGFBP5 in the case of methylation in breast cancer. METHODS: We used methyl-specific polymerase (MSP) chain reaction to detect CpG methylation of IGFBP5 promoter and exon-I in breast cancer and adjacent tissues. Gene expression is evaluated by quantative polymerase chain reaction (qPCR). RESULTS: IGFBP5 methylation was detected in 24 of 58 (41%) and 54 of 56 (96.5%) promoter and exon-I site respectively in tumor tissues. In adjacent tissues 17 of 58 (29%) and 53 of 56 (96.5%) was methylated. IGFBP5 expression was higher estrogene receptor (ER)(+) than ER(-) patients (p = 0:0549). Beside, we found a positive correlation between the expression of IGFBP5 and G2 tumor grade (p = 0:0131). However, no correlation was observed between IGFBP5 expression and age, menopause or the presence of lymph node metastasis (p > 0:05). CONCLUSIONS: In summary, our results showed that IGFBP5 promoter and exon-I methylation did not have any differences between tumor and adjacent tissues so that IGFBP5 methylation did not change IGFBP5 gene regulation in breast cancer. This is the first study investigating the IGFBP5 gene methylation in breast cancer.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/bayburt/13893Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.3233/bd-160234Yayıncı resmi DOI adresi
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9
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorKarabulut, Sevgi
dc.contributor.authorKaya, Zehra
dc.contributor.authorAmuran, Gökçe Gullu
dc.contributor.authorPeker, Irem
dc.contributor.authorÖzmen, Tolga
dc.contributor.authorGulluolu, Bahadir M.
dc.contributor.authorKaya, Handan
dc.contributor.authorErzik, Can
dc.contributor.authorOzer, Ayşe
dc.contributor.authorAkkiprik, Mustafa
dc.date.accessioned2026-10-29T19:11:36.107140487Z
dc.date.available2026-10-29T19:11:36.107140487Z
dc.date.issued2016
dc.description.abstractBACKGROUND: The insulin-like growth factor binding protein5 (IGFBP5) is often dysregulated in human cancers and considered neither a tumor suppressor nor an oncogene. OBJECTIVE: We aim to examine the reason of the changeable gene regulation of IGFBP5 in the case of methylation in breast cancer. METHODS: We used methyl-specific polymerase (MSP) chain reaction to detect CpG methylation of IGFBP5 promoter and exon-I in breast cancer and adjacent tissues. Gene expression is evaluated by quantative polymerase chain reaction (qPCR). RESULTS: IGFBP5 methylation was detected in 24 of 58 (41%) and 54 of 56 (96.5%) promoter and exon-I site respectively in tumor tissues. In adjacent tissues 17 of 58 (29%) and 53 of 56 (96.5%) was methylated. IGFBP5 expression was higher estrogene receptor (ER)(+) than ER(-) patients (p = 0:0549). Beside, we found a positive correlation between the expression of IGFBP5 and G2 tumor grade (p = 0:0131). However, no correlation was observed between IGFBP5 expression and age, menopause or the presence of lymph node metastasis (p > 0:05). CONCLUSIONS: In summary, our results showed that IGFBP5 promoter and exon-I methylation did not have any differences between tumor and adjacent tissues so that IGFBP5 methylation did not change IGFBP5 gene regulation in breast cancer. This is the first study investigating the IGFBP5 gene methylation in breast cancer.
dc.identifier.doi10.3233/bd-160234
dc.identifier.endpage131
dc.identifier.issn0888-6008
dc.identifier.issue4
dc.identifier.pmid27612043
dc.identifier.scopus2-s2.0-85008616079
dc.identifier.startpage123
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/13893
dc.identifier.volume36
dc.language.isoen
dc.publisherIOS Press
dc.relation.ispartofBreast Disease
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectbreast cancer
dc.subjectIGFBP5
dc.subjectmethylation
dc.subjectMSP
dc.subjectpromoter
dc.subject.otherAdult
dc.subject.otherAged
dc.subject.otherBreast Neoplasms
dc.subject.otherCpG Islands
dc.subject.otherDNA Methylation
dc.subject.otherExons
dc.subject.otherFemale
dc.subject.otherGene Expression
dc.subject.otherGene Expression Regulation, Neoplastic
dc.subject.otherHumans
dc.subject.otherInsulin-Like Growth Factor Binding Protein 5
dc.subject.otherMiddle Aged
dc.subject.otherNeoplasm Grading
dc.subject.otherPolymerase Chain Reaction
dc.subject.otherPromoter Regions, Genetic
dc.subject.otherReceptor, ErbB-2
dc.subject.otherReceptors, Estrogen
dc.subject.otherReceptors, Progesterone
dc.subject.otherRNA, Messenger
dc.subject.otherbeta actin
dc.subject.otherepidermal growth factor receptor 2
dc.subject.otherestrogen receptor
dc.subject.otherKi 67 antigen
dc.subject.othersomatomedin binding protein 5
dc.subject.otherERBB2 protein, human
dc.subject.othermessenger RNA
dc.subject.otherprogesterone receptor
dc.subject.otherage distribution
dc.subject.otherArticle
dc.subject.otherbinding site
dc.subject.otherbreast cancer
dc.subject.othercancer grading
dc.subject.othercancer prognosis
dc.subject.othercontrolled study
dc.subject.otherCpG island
dc.subject.othergene expression regulation
dc.subject.othergene sequence
dc.subject.otherhistopathology
dc.subject.otherhuman
dc.subject.otherhuman tissue
dc.subject.otherlymph node metastasis
dc.subject.othermajor clinical study
dc.subject.otherpostmenopause
dc.subject.otherpriority journal
dc.subject.otherpromoter region
dc.subject.otherprotein expression
dc.subject.othertranscription initiation site
dc.subject.otherbreast tumor
dc.subject.otherexon
dc.subject.othergenetics
dc.subject.othermetabolism
dc.subject.otherpathology
dc.titleCorrelation between the DNA methylation and gene expression of IGFBP5 in breast cancer
dc.typeArticle
rdl.citation.scopus9
rdl.departmentMarmara University, School of Medicine, Medical Biology Department, Istanbul, Turkey
rdl.departmentBayburt University, Health Services Vocational School, Bayburt, Turkey
rdl.departmentYüzüncü Yıl University, School of Medicine, Medical Biology Department, Van, Turkey
rdl.departmentMarmara University, School of Medicine, General Surgery Department, Istanbul, Turkey
rdl.departmentMarmara University, School of Medicine, Pathology Department, Istanbul, Turkey
rdl.oa.statusclosed
rdl.oa.statusgreen
rdl.oa.urlhttps://hdl.handle.net/20.500.12403/668
rdl.scopus.quartileQ3
rdl.source.indexSCOPUS
rdl.source.indexPUBMED