Hochschulschrift

VHL and Hypoxia regulated genes in sympatho-adrenal cell lineage development and disease

Zusammenfassung: VHL and Hypoxia regulated genes in sympatho- adrenal cell lineage Development and DiseaseAbstractCells of the sympatho-adrenal (SA) cell lineage develop from neural crest cells (NCCs). Abnormal development of SA cells has been linked to various tumors, including neuroblastoma (NB), and Pheochromocytoma (PCC). In humans mutations of the Von Hippel Lindau tumor suppressor gene (VHL), a negative regulator of hypoxia inducible factors, is one of the major causes of PCC development. .Mammalian embryos develop within a hypoxic environment, under the influence of hypoxia inducible factors (HIFs). HIFs have been linked to various diseases, including NB, due to their impact on cellular differentiation. Delta like homolog 1 (DLK-1) is another gene implicated in neuroblastoma, which is hypoxia regulated and lies downstream of HIF system. However, the main role of VHL and hypoxia-inducible factors during normal development of SA cells is unclear up to date.The aim of the current study was to investigate the in vivo role of VHL on the normal development of SA cells and to investigate, whether the loss of VHL function leads to SA derived tumor development as pheochromocytoma.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Albert-Ludwigs-Universität Freiburg, Dissertation, 2016

Schlagwort
Krebs
Onkologie

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2016
Urheber
Beteiligte Personen und Organisationen

DOI
10.6094/UNIFR/11085
URN
urn:nbn:de:bsz:25-freidok-110851
Rechteinformation
Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
25.03.2025, 13:56 MEZ

Datenpartner

Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.

Objekttyp

  • Hochschulschrift

Beteiligte

Entstanden

  • 2016

Ähnliche Objekte (12)