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Verfasst von:Stefanovic, Stefan [VerfasserIn]   i
 Deutsch, Thomas M. [VerfasserIn]   i
 Sinn, Peter [VerfasserIn]   i
 Schütz, Florian [VerfasserIn]   i
 Bohlmann, Michael K. [VerfasserIn]   i
 Sütterlin, Marc [VerfasserIn]   i
 Schneeweiss, Andreas [VerfasserIn]   i
 Wallwiener, Markus [VerfasserIn]   i
Titel:Molecular subtype conversion between primary and metastatic breast cancer corresponding to the dynamics of apoptotic and intact circulating tumor cells
Verf.angabe:Stefan Stefanovic, Thomas M. Deutsch, Ralph Wirtz, Andreas Hartkopf, Peter Sinn, Florian Schuetz, Christof Sohn, Michael K. Bohlmann, Marc Sütterlin, Andreas Schneeweiss and Markus Wallwiener
E-Jahr:2019
Jahr:11 March 2019
Umfang:10 S.
Fussnoten:Gesehen am 06.12.2019
Titel Quelle:Enthalten in: Cancers
Ort Quelle:Basel : MDPI, 2009
Jahr Quelle:2019
Band/Heft Quelle:11(2019,3) Artikel-Nummer 342, 10 Seiten
ISSN Quelle:2072-6694
Abstract:The presence of circulating tumor cells (CTCs), detected as a form of liquid biopsy is associated with poor survival in both early and metastatic breast cancer. Monitoring tumor biology based on intrinsic subtypes delivers treatment-relevant information on the heterogeneity or biomarker conversion between primary and metastatic tumors. This study aimed to correlate the change of the apoptotic and intact CTC counts with mRNA-assessed intrinsic subtype change. Thirty-four breast cancer patients with available triplets of primary tumors, distant metastasis biopsies and data on intact and apoptotic CTC dynamics were included in the analysis. The intrinsic subtype was determined per RT-qPCR quantification of the gene expression ESR1, PGR, ERBB2 and MKI67. Both luminal (p = 0.038) and triple negative (p = 0.035) patients showed a significant downregulation of apoptotic CTCs. Repeated biopsies of distant metastatic sites, as well as determining a potential shift of the intrinsic subtype, combined with data on intact and apoptotic CTC dynamics from liquid biopsies might help personalize systemic therapy and generate additional surrogate markers for successful systemic therapy.
DOI:doi:10.3390/cancers11030342
URL:kostenfrei: Volltext: https://doi.org/10.3390/cancers11030342
 kostenfrei: Verlag: https://www.mdpi.com/2072-6694/11/3/342
 DOI: https://doi.org/10.3390/cancers11030342
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:biomarker conversion
 breast cancer
 circulating tumor cells
 intrinsic subtype
 RT-qPCR
K10plus-PPN:1684618967
Verknüpfungen:→ Zeitschrift
 
 
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