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1000 Titel
  • C20orf204, a hepatocellular carcinoma-specific protein interacts with nucleolin and promotes cell proliferation
1000 Autor/in
  1. Burbano De Lara, Sebastian |
  2. Tran, Doan Duy Hai |
  3. Allister, Bernardus Aldrige |
  4. Polenkowski, Mareike |
  5. Nashan, Björn |
  6. Koch, Martina |
  7. Tamura, Teruko |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-03-17
1000 Erschienen in
1000 Quellenangabe
  • 10(3):31
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1038/s41389-021-00320-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969625/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • In most human cancers, a large number of proteins with driver mutations are involved in tumor development, implying that multiple fine tuners are involved in cancer formation and/or maintenance. A useful strategy for cancer therapy may therefore be to target multiple cancer type-specific fine tuners. Furthermore, genome-wide association studies of tumor samples have identified a large number of long noncoding (lnc)RNA associated with various types of tumor. In this context we have previously found that C20orf204 (a splice variant of Linc00176) RNA contains a 189 amino acid (AA) long open reading frame (C20orf204-189AA) that is expressed predominantly in hepatocellular carcinoma (HCC). We report here that a protein, C20orf204-189AA, was detected in the nucleus of 14 out of 20 primary HCC, but not in control livers. Strikingly, overexpression of C20orf204-189AA enhanced cell proliferation and ribosomal RNA transcription. C20orf204-189AA is co-localized, and interacted with nucleolin via the C-terminal and with ribosomal RNA via the N-terminal domain. Furthermore, the expression of C20orf204-189AA upregulates the protein level of nucleolin. Nucleolin and C20orf204 mRNA levels in HCC are correlated with tumor differentiation grade and patient survival, suggesting that C20orf204-189AA is a cancer type-specific fine tuner in some HCC that presents itself for potential targeting therapy and cancer biomarker. Thus, cancer cells exhibit remarkable transcriptome alterations partly by adopting cancer-specific splicing isoforms of noncoding RNAs and may participate in tumor development.
1000 Sacherschließung
lokal Molecular biology
lokal Article
lokal Cancer
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-5364-2686|https://frl.publisso.de/adhoc/uri/VHJhbiwgRG9hbiBEdXkgSGFp|https://orcid.org/0000-0003-1712-5937|https://orcid.org/0000-0003-3278-464X|https://orcid.org/0000-0001-7587-9935|https://frl.publisso.de/adhoc/uri/S29jaCwgTWFydGluYQ==|https://orcid.org/0000-0003-1069-8652
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1000 Erstellt am 2023-04-26T15:10:10.240+0200
1000 Erstellt von 322
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1000 Zuletzt bearbeitet 2023-10-19T12:59:28.050+0200
1000 Objekt bearb. Thu Oct 19 12:59:28 CEST 2023
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