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Status: Bibliographieeintrag

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Verfasst von:Salnikov, Alexey V. [VerfasserIn]   i
 Liu, Li [VerfasserIn]   i
 Platen, Mitja [VerfasserIn]   i
 Gladkich, Jury [VerfasserIn]   i
 Salnikova, Olga [VerfasserIn]   i
 Ryschich, Eduard [VerfasserIn]   i
 Mattern, Jürgen [VerfasserIn]   i
 Moldenhauer, Gerhard [VerfasserIn]   i
 Werner, Jens [VerfasserIn]   i
 Schemmer, Peter [VerfasserIn]   i
 Büchler, Markus W. [VerfasserIn]   i
 Herr, Ingrid [VerfasserIn]   i
Titel:Hypoxia induces EMT in low and highly aggressive pancreatic tumor cells but only cells with cancer stem cell characteristics acquire pronounced migratory potential
Verf.angabe:Alexei V. Salnikov, Li Liu, Mitja Platen, Jury Gladkich, Olga Salnikova, Eduard Ryschich, Jürgen Mattern, Gerhard Moldenhauer, Jens Werner, Peter Schemmer, Markus W. Büchler, Ingrid Herr
Jahr:2012
Umfang:9 S.
Fussnoten:Published September 26, 2012 ; Gesehen am 25.06.2018
Titel Quelle:Enthalten in: PLOS ONE
Ort Quelle:San Francisco, California, US : PLOS, 2006
Jahr Quelle:2012
Band/Heft Quelle:7(2012,9), Artikel-Nummer e46391, 9 Seiten
ISSN Quelle:1932-6203
Abstract:Tumor hypoxia induces epithelial-mesenchymal transition (EMT), which induces invasion and metastasis, and is linked to cancer stem cells (CSCs). Whether EMT generates CSCs de novo, enhances migration of existing CSCs or both is unclear. We examined patient tissue of pancreatic ductal adenocarcinoma (PDA) along with carcinomas of breast, lung, kidney, prostate and ovary. For in vitro studies, five established PDA cell lines classified as less (CSClow) and highly aggressive CSC-like cells (CSChigh) were examined by single and double immunofluorescence microscopy, wound-, transwell-, and time-lapse microscopy. HIF-1α and Slug, as well as HIF-2α and CD133 were co-expressed pointing to a putative co-existence of hypoxia, EMT and CSCs in vivo. CSChigh cells exhibited high basal expression of the mesenchymal Vimentin protein but low or absent expression of the epithelial marker E-cadherin, with the opposite result in CSClow cells. Hypoxia triggered altering of cell morphology from an epithelial to a mesenchymal phenotype, which was more pronounced in CSChigh cells. Concomitantly, E-cadherin expression was reduced and expression of Vimentin, Slug, Twist2 and Zeb1 enhanced. While hypoxia caused migration in all cell lines, velocity along with the percentage of migrating, polarized and pseudopodia-forming cells was significantly higher in CSChigh cells. These data indicate that hypoxia-induced EMT occurs in PDA and several other tumor entities. However although hypoxia-induced EMT signaling occurs in all tumor cell populations, only the stem-like cells acquire high migratory potential and thus may be responsible for invasion and metastasis.
DOI:doi:10.1371/journal.pone.0046391
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kostenfrei: Volltext: http://dx.doi.org/10.1371/journal.pone.0046391
 kostenfrei: Volltext: http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0046391
 DOI: https://doi.org/10.1371/journal.pone.0046391
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Cancer cell migration
 Cancer stem cells
 Cell migration
 Hypoxia
 Medical hypoxia
 Metastasis
 Pancreatic cancer
 Vimentin
K10plus-PPN:1576815234
Verknüpfungen:→ Zeitschrift

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