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1000 Titel
  • Downregulation of SFRP1 is a protumorigenic event in hepatoblastoma and correlates with beta-catenin mutations
1000 Autor/in
  1. Regel, Ivonne |
  2. Eichenmüller, Melanie |
  3. Mahajan, Ujjwal Mukund |
  4. Hagl, Beate |
  5. Benitz, Simone |
  6. Häberle, Beate |
  7. Vokuhl, Christian |
  8. von Schweinitz, Dietrich |
  9. Kappler, Roland |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-03-18
1000 Erschienen in
1000 Quellenangabe
  • 146(5):1153-1167
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00432-020-03182-1 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142044/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Hepatoblastoma (HB) and pediatric hepatocellular carcinoma (HCC) are the most common malignant liver tumors in childhood. Both tumor types exhibit genetic and epigenetic alterations in the WNT/β-catenin signaling pathway, which is a key regulator of liver progenitor cells in embryonic development. The tumors demonstrate a high rate of β-catenin mutations and gene expression changes of several WNT antagonists. However, the role of the WNT inhibitory factor secreted frizzled-related protein 1 (SFRP1) has not been addressed in pediatric liver cancer so far.!##!Results!#!In our study, we investigated the gene expression level, DNA methylation status and functional relevance of SFRP1 in HB cell lines and in pediatric liver tumor patient samples. SFRP1 was downregulated due to DNA promoter methylation in all tested HB cell lines. Overexpression of SFRP1 in HB cell lines diminished tumor cell proliferation, colony formation and migration potential. In addition, the SFRP1-expressing HB cell lines showed reduced WNT/β-catenin signaling pathway activity and decreased expression of WNT target genes. To evaluate the utility of SFRP1 as a biomarker in pediatric liver cancer, we determined the gene expression level and DNA methylation status of SFRP1 in 45 pediatric liver tumor patient samples. The correlation analysis of different clinical parameters and tumor characteristics revealed a significant correlation of reduced SFRP1 expression with the presence of mutant β-catenin. The methylation status of SFRP1 was furthermore associated to a pediatric liver tumor type with HCC-like characteristics, TERT mutations and an older age at diagnosis.!##!Conclusion!#!Altogether, our data demonstrate that the epigenetic suppression of the WNT/β-catenin antagonist SFRP1 has an important impact on the malignant behavior of HB cells. Although SFRP1 methylation is a common event in HCC-like pediatric liver tumors, its potential as a prognostic or diagnostic biomarker needs to be further investigated.
1000 Sacherschließung
lokal Cell Line, Tumor [MeSH]
lokal Aged [MeSH]
lokal SFRP1
lokal DKK1
lokal Intercellular Signaling Peptides and Proteins/genetics [MeSH]
lokal beta Catenin/genetics [MeSH]
lokal APC
lokal Wnt Signaling Pathway [MeSH]
lokal WNT signaling
lokal Liver Neoplasms/metabolism [MeSH]
lokal Male [MeSH]
lokal Hepatoblastoma/genetics [MeSH]
lokal DNA methylation
lokal WIF1
lokal Liver Neoplasms/genetics [MeSH]
lokal Intercellular Signaling Peptides and Proteins/biosynthesis [MeSH]
lokal Hepatoblastoma/metabolism [MeSH]
lokal Membrane Proteins/genetics [MeSH]
lokal Female [MeSH]
lokal beta Catenin/metabolism [MeSH]
lokal Mutation [MeSH]
lokal Down-Regulation [MeSH]
lokal Original Article – Cancer Research
lokal Humans [MeSH]
lokal Hepatocellular carcinoma
lokal Middle Aged [MeSH]
lokal Hep G2 Cells [MeSH]
lokal Membrane Proteins/biosynthesis [MeSH]
lokal DNA Methylation [MeSH]
lokal Epigenetics
lokal Pediatric liver cancer
lokal Hepatoblastoma
lokal Promoter Regions, Genetic [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/UmVnZWwsIEl2b25uZQ==|https://frl.publisso.de/adhoc/uri/RWljaGVubcO8bGxlciwgTWVsYW5pZQ==|https://frl.publisso.de/adhoc/uri/TWFoYWphbiwgVWpqd2FsIE11a3VuZA==|https://frl.publisso.de/adhoc/uri/SGFnbCwgQmVhdGU=|https://frl.publisso.de/adhoc/uri/QmVuaXR6LCBTaW1vbmU=|https://frl.publisso.de/adhoc/uri/SMOkYmVybGUsIEJlYXRl|https://frl.publisso.de/adhoc/uri/Vm9rdWhsLCBDaHJpc3RpYW4=|https://frl.publisso.de/adhoc/uri/dm9uIFNjaHdlaW5pdHosIERpZXRyaWNo|https://frl.publisso.de/adhoc/uri/S2FwcGxlciwgUm9sYW5k
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1000 Erstellt am 2023-11-17T11:37:12.717+0100
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