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1000 Titel
  • Prognostic significance of high mobility group A2 (HMGA2) in pancreatic ductal adenocarcinoma: malignant functions of cytoplasmic HMGA2 expression
1000 Autor/in
  1. Gundlach, Jan-Paul |
  2. Hauser, Charlotte |
  3. Schlegel, Franka Maria |
  4. Willms, Anna |
  5. Halske, Christine |
  6. Röder, Christian |
  7. Krüger, Sandra |
  8. Röcken, Christoph |
  9. Becker, Thomas |
  10. Kalthoff, Holger |
  11. Trauzold, Anna |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-24
1000 Erschienen in
1000 Quellenangabe
  • 147(11):3313-3324
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00432-021-03745-w |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484217/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!HMGA2 has frequently been found in benign as well as malignant tumors and a significant association between HMGA2 overexpression and poor survival in different malignancies was described. In pancreatic ductal adenocarcinoma (PDAC), nuclear HMGA2 expression is associated with tumor dedifferentiation and presence of lymph node metastasis. Nevertheless, the impact of HMGA2 occurrence in other cell compartments is unknown.!##!Methods!#!Intracellular distribution of HMGA2 was analyzed in PDAC (n = 106) and peritumoral, non-malignant ducts (n = 28) by immunohistochemistry. Findings were correlated with clinico-pathological data. Additionally, intracellular HMGA2 presence was studied by Western blotting of cytoplasmic and nuclear fractions of cultured cells.!##!Results!#!HMGA2 was found in the cytoplasm and in the nucleus of cultured cells. In human tumor tissue, HMGA2 was also frequently found in the cytoplasm and the nucleus of tumor cells, however, nuclear staining was generally stronger. Direct comparison from tumor tissue with corresponding non-neoplastic peritumoral tissue revealed significantly stronger expression in tumors (p = 0.003). Of note, the nuclear staining was significantly stronger in lymph node metastatic cell nuclei compared to primary tumor cell nuclei (p = 0.049). Interestingly, cytoplasmic staining positively correlated with lymph vessel (p = 0.004) and venous invasion (p = 0.046).!##!Conclusion!#!HMGA2 is a prognostic marker in PDAC. Firstly, we found a positive correlation for cytoplasmic HMGA2 expression with lympho-vascular invasion and, secondly, we found a significantly stronger nuclear expression of HMGA2 in cancer-positive lymph node nuclei compared to primary tumor cell nuclei. So far, the role of cytoplasmic HMGA2 is nearly unknown, however, our data lend support to the hypothesis that cytoplasmic HMGA2 expression is involved in nodal spread.
1000 Sacherschließung
lokal Female [MeSH]
lokal Cell Line, Tumor [MeSH]
lokal Aged, 80 and over [MeSH]
lokal Aged [MeSH]
lokal Immunohistology
lokal Original Article – Cancer Research
lokal Cell Nucleus/metabolism [MeSH]
lokal Nucleus
lokal Humans [MeSH]
lokal Middle Aged [MeSH]
lokal Cytoplasm/metabolism [MeSH]
lokal Prognosis
lokal HMGA2 Protein/biosynthesis [MeSH]
lokal HMGA2
lokal Male [MeSH]
lokal Prognosis [MeSH]
lokal Pancreatic Neoplasms/metabolism [MeSH]
lokal Colonic Neoplasms/metabolism [MeSH]
lokal HCT116 Cells [MeSH]
lokal Carcinoma, Pancreatic Ductal/metabolism [MeSH]
lokal Pancreatic cancer
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-8845-6832|https://frl.publisso.de/adhoc/uri/SGF1c2VyLCBDaGFybG90dGU=|https://frl.publisso.de/adhoc/uri/U2NobGVnZWwsIEZyYW5rYSBNYXJpYQ==|https://frl.publisso.de/adhoc/uri/V2lsbG1zLCBBbm5h|https://frl.publisso.de/adhoc/uri/SGFsc2tlLCBDaHJpc3RpbmU=|https://frl.publisso.de/adhoc/uri/UsO2ZGVyLCBDaHJpc3RpYW4=|https://frl.publisso.de/adhoc/uri/S3LDvGdlciwgU2FuZHJh|https://frl.publisso.de/adhoc/uri/UsO2Y2tlbiwgQ2hyaXN0b3Bo|https://frl.publisso.de/adhoc/uri/QmVja2VyLCBUaG9tYXM=|https://frl.publisso.de/adhoc/uri/S2FsdGhvZmYsIEhvbGdlcg==|https://frl.publisso.de/adhoc/uri/VHJhdXpvbGQsIEFubmE=
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1000 Erstellt am 2023-05-09T10:16:55.071+0200
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1000 Zuletzt bearbeitet 2023-10-21T01:58:54.342+0200
1000 Objekt bearb. Sat Oct 21 01:58:54 CEST 2023
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