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1000 Titel
  • Dysregulated paired related homeobox 1 impacts on hepatocellular carcinoma phenotypes
1000 Autor/in
  1. Piorońska, Weronika |
  2. Nwosu, Zeribe Chike |
  3. Han, Mei |
  4. Büttner, Michael |
  5. Ebert, Matthias Philip |
  6. Dooley, Steven |
  7. Meyer, Christoph |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-09-08
1000 Erschienen in
1000 Quellenangabe
  • 21(1):1006
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12885-021-08637-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424914/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Hepatocellular carcinoma (HCC) is a major cause of cancer-related death. Paired related homeobox 1 (PRRX1) is a transcription factor that regulates cell growth and differentiation, but its importance in HCC is unclear.!##!Methods!#!We examined the expression pattern of PRRX1 in nine microarray datasets of human HCC tumour samples (n > 1100) and analyzed its function in HCC cell lines. In addition, we performed gene set enrichment, Kaplan-Meier overall survival analysis, metabolomics and functional assays.!##!Results!#!PRRX1 is frequently upregulated in human HCC. Pathway enrichment analysis predicted a direct correlation between PRRX1 and focal adhesion and epithelial-mesenchymal transition. High expression of PRRX1 and low ZEB1 or high ZEB2 significantly predicted better overall survival in HCC patients. In contrast, metabolic processes correlated inversely and transcriptional analyses revealed that glycolysis, TCA cycle and amino acid metabolism were affected. These findings were confirmed by metabolomics analysis. At the phenotypic level, PRRX1 knockdown accelerated proliferation and clonogenicity in HCC cell lines.!##!Conclusions!#!Our results suggest that PRRX1 controls metabolism, has a tumour suppressive role, and may function in cooperation with ZEB1/2. These findings have functional relevance in HCC, including in understanding transcriptional control of distinct cancer hallmarks.
1000 Sacherschließung
lokal Gene Expression Regulation, Neoplastic [MeSH]
lokal Carcinoma, Hepatocellular/metabolism [MeSH]
lokal Tumor Cells, Cultured [MeSH]
lokal Liver Neoplasms/pathology [MeSH]
lokal Liver Neoplasms/metabolism [MeSH]
lokal Liver cancer
lokal Metabolome [MeSH]
lokal EMT
lokal Phenotype [MeSH]
lokal Metabolism
lokal Liver Neoplasms/genetics [MeSH]
lokal Cell Proliferation [MeSH]
lokal Humans [MeSH]
lokal Carcinoma, Hepatocellular/pathology [MeSH]
lokal Epithelial-Mesenchymal Transition [MeSH]
lokal Homeodomain Proteins/genetics [MeSH]
lokal Survival Rate [MeSH]
lokal Carcinoma, Hepatocellular/genetics [MeSH]
lokal Biomarkers, Tumor/metabolism [MeSH]
lokal Homeodomain Proteins/metabolism [MeSH]
lokal Research
lokal Biomarkers, Tumor/genetics [MeSH]
lokal PRRX1
lokal Prognosis [MeSH]
lokal Epithelial mesenchymal transition
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/UGlvcm-FhHNrYSwgV2Vyb25pa2E=|https://frl.publisso.de/adhoc/uri/Tndvc3UsIFplcmliZSBDaGlrZQ==|https://frl.publisso.de/adhoc/uri/SGFuLCBNZWk=|https://frl.publisso.de/adhoc/uri/QsO8dHRuZXIsIE1pY2hhZWw=|https://frl.publisso.de/adhoc/uri/RWJlcnQsIE1hdHRoaWFzIFBoaWxpcA==|https://frl.publisso.de/adhoc/uri/RG9vbGV5LCBTdGV2ZW4=|https://frl.publisso.de/adhoc/uri/TWV5ZXIsIENocmlzdG9waA==
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1000 Erstellt am 2023-11-15T17:11:16.947+0100
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1000 Zuletzt bearbeitet Thu Nov 30 21:13:02 CET 2023
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