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Verfasst von:Fischer, Chiara [VerfasserIn]   i
 Turchinovich, Andrey [VerfasserIn]   i
 Feißt, Manuel [VerfasserIn]   i
 Riedel, Fabian [VerfasserIn]   i
 Haßdenteufel, Kathrin [VerfasserIn]   i
 Scharli, Philipp [VerfasserIn]   i
 Hartkopf, Andreas [VerfasserIn]   i
 Brucker, Sara [VerfasserIn]   i
 Michel, Laura L. [VerfasserIn]   i
 Burwinkel, Barbara [VerfasserIn]   i
 Schneeweiss, Andreas [VerfasserIn]   i
 Wallwiener, Markus [VerfasserIn]   i
 Deutsch, Thomas M. [VerfasserIn]   i
Titel:Circulating miR-200 family and CTCs in metastatic breast cancer before, during, and after a new line of systemic treatment
Verf.angabe:Chiara Fischer, Andrey Turchinovich, Manuel Feisst, Fabian Riedel, Kathrin Haßdenteufel, Philipp Scharli, Andreas D. Hartkopf, Sara Y. Brucker, Laura Michel, Barbara Burwinkel, Andreas Schneeweiss, Markus Wallwiener and Thomas M. Deutsch
E-Jahr:2022
Jahr:23 August 2022
Umfang:12 S.
Fussnoten:Gesehen am 20.10.2022
Titel Quelle:Enthalten in: International journal of molecular sciences
Ort Quelle:Basel : Molecular Diversity Preservation International, 2000
Jahr Quelle:2022
Band/Heft Quelle:23(2022), 17, Artikel-ID 9535, Seite 1-12
ISSN Quelle:1422-0067
 1661-6596
Abstract:The extracellular circulating microRNA (miR)-200 regulates epithelial-mesenchymal transition and, thus, plays an essential role in the metastatic cascade and has shown itself to be a promising prognostic and predictive biomarker in metastatic breast cancer (MBC). Expression levels of the plasma miR-200 family were analyzed in relationship to systemic treatment, circulating tumor cells (CTC) count, progression-free survival (PFS), and overall survival (OS). Expression of miR-200a, miR-200b, miR-200c, miR-141, and miR-429, and CTC status (CTC-positive ≥ 5 CTC/7.5 mL) was assessed in 47 patients at baseline (BL), after the first completed cycle of a new line of systemic therapy (1C), and upon the progression of disease (PD). MiR-200a, miR-200b, and miR-141 expression was reduced at 1C compared to BL. Upon PD, all miR-200s were upregulated compared to 1C. At all timepoints, the levels of miR-200s were elevated in CTC-positive versus CTC-negative patients. Further, heightened miR-200s expression and positive CTC status were associated with poorer OS at BL and 1C. In MBC patients, circulating miR-200 family members decreased after one cycle of a new line of systemic therapy, were elevated during PD, and were indicative of CTC status. Notably, increased levels of miR-200s and elevated CTC count correlated with poorer OS and PFS. As such, both are promising biomarkers for optimizing the clinical management of MBC.
DOI:doi:10.3390/ijms23179535
URL:kostenfrei: Volltext: https://doi.org/10.3390/ijms23179535
 kostenfrei: Volltext: https://www.mdpi.com/1422-0067/23/17/9535
 DOI: https://doi.org/10.3390/ijms23179535
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:circulating microRNA
 circulating tumor cells
 CTC
 EMT
 epithelial-mesenchymal transition
 MBC
 metastatic breast cancer
 microRNA-200 family
 miR-200 family
 miR-200s
K10plus-PPN:1819460215
Verknüpfungen:→ Zeitschrift
 
 
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