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2020-02-18Zeitschriftenartikel DOI: 10.25646/6579
Upregulation of SMYD3 and SMYD3 VNTR 3/3 polymorphism increase the risk of hepatocellular carcinoma
dc.contributor.authorThanh Binh, Mai
dc.contributor.authorXuan Hoan, Nghiem
dc.contributor.authorPhuong Giang, Dao
dc.contributor.authorVan Tong, Hoang
dc.contributor.authorBock, Claus-Thomas
dc.contributor.authorWedemeyer, Heiner
dc.contributor.authorLinh Toan, Nguyen
dc.contributor.authorHong Bang, Mai
dc.contributor.authorKremsner, Peter G.
dc.contributor.authorMeyer, Christian G.
dc.contributor.authorHuu Song, Le
dc.contributor.authorVelavan, Thirumalaisamy P.
dc.date.accessioned2020-03-23T07:44:43Z
dc.date.available2020-03-23T07:44:43Z
dc.date.issued2020-02-18none
dc.identifier.other10.1038/s41598-020-59667-z
dc.identifier.urihttp://edoc.rki.de/176904/6546
dc.description.abstractSMYD3 (SET and MYND domain-containing protein 3) is involved in histone modification, which initiates oncogenesis by activating transcription of multiple downstream genes. To investigate associations of variable numbers of tandem repeats (VNTR) variants in the SMYD3 gene promoter, SMYD3 serum levels and SMYD3 mRNA expression in hepatitis B virus (HBV) infection and clinical progression of related liver disease. SMYD3 VNTRs were genotyped in 756 HBV patients and 297 healthy controls. SMYD3 serum levels were measured in 293 patients and SMYD3 mRNA expression was quantified in 48 pairs of hepatocellular tumor and adjacent non-tumor liver tissues. Genotype SYMD3 VNTR 3/3 was more frequent among HCC patients than in controls (Padjusted = 0.037). SMYD3 serum levels increased according to clinical progression of liver diseases (P = 0.01); HCC patients had higher levels than non-HCC patients (P = 0.04). Among patients with SMYD3 VNTR 3/3, HCC patients had higher SMYD3 levels than others (P < 0.05). SMYD3 mRNA expression was up-regulated in HCC tumor tissues compared to other tissues (P = 0.008). In conclusion, upregulation of SMYD3 correlates with the occurrence of HCC and SMYD3 VNTR 3/3 appears to increase the risk of HCC through increasing SMYD3 levels. SMYD3 may be an indicator for HCC development in HBV patients.eng
dc.language.isoengnone
dc.publisherRobert Koch-Institut
dc.rights(CC BY 3.0 DE) Namensnennung 3.0 Deutschlandger
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/de/
dc.subjectHepatitis Beng
dc.subjectHepatocellular carcinomaeng
dc.subject.ddc610 Medizin und Gesundheitnone
dc.titleUpregulation of SMYD3 and SMYD3 VNTR 3/3 polymorphism increase the risk of hepatocellular carcinomanone
dc.typearticle
dc.identifier.urnurn:nbn:de:kobv:0257-176904/6546-4
dc.identifier.doihttp://dx.doi.org/10.25646/6579
dc.type.versionpublishedVersionnone
local.edoc.container-titleScientific Reportsnone
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttps://www.nature.com/articles/s41598-020-59667-z#Abs1none
local.edoc.container-publisher-nameSpringer Naturenone
local.edoc.container-volume10none
local.edoc.container-issue2797none
local.edoc.container-year2020none
local.edoc.container-firstpage1none
local.edoc.container-lastpage8none
local.edoc.rki-departmentInfektionskrankheitennone
dc.description.versionPeer Reviewednone

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