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Erschienen in: Clinical & Experimental Metastasis 8/2012

01.12.2012 | Research Paper

CD44+/CD24− ovarian cancer cells demonstrate cancer stem cell properties and correlate to survival

verfasst von: Erhong Meng, Beverely Long, Paula Sullivan, Steve McClellan, Michael A. Finan, Eddie Reed, Lalita Shevde, Rodney P. Rocconi

Erschienen in: Clinical & Experimental Metastasis | Ausgabe 8/2012

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Abstract

Cancer cells with the surface marker profile CD44+/CD24− have previously been described to possess cancer stem cell-like properties. This manuscript evaluates those properties in ovarian cancer cell lines. The proportion of CD44+/CD24− cells corresponded to the clinical aggressiveness of each ovarian cancer cell line histologic subtype. CD44+/CD24− cells demonstrated enhanced progressive differentiation as well as showing a 60-fold increase in Matrigel invasion in both SKOV3 and OV90 cell lines (p < 0.001 each) compared to other phenotypes. CD44+/CD24− demonstrated significant resistance to all chemotherapy agents used in all cell lines, with a 71–93 % increase in resistance compared with baseline. Using a threshold of 25 % CD44+/CD24– ovarian cancer cells found in ascites, patients with >25 % CD44+/CD24− were significantly more likely to recur (83 vs. 14 %, p = 0.003) and had shorter median progression-free survival (6 vs. 18 months, p = 0.01). In conclusion, the CD44+/CD24− phenotype in ovarian cancer cells demonstrate cancer stem cell-like properties of enhanced differentiation, invasion, and resistance to chemotherapy. This CD44+/CD24− phenotype correlates to clinical endpoints with increased risk of recurrence and shorter progression-free survival in patients with ovarian cancer.
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Metadaten
Titel
CD44+/CD24− ovarian cancer cells demonstrate cancer stem cell properties and correlate to survival
verfasst von
Erhong Meng
Beverely Long
Paula Sullivan
Steve McClellan
Michael A. Finan
Eddie Reed
Lalita Shevde
Rodney P. Rocconi
Publikationsdatum
01.12.2012
Verlag
Springer Netherlands
Erschienen in
Clinical & Experimental Metastasis / Ausgabe 8/2012
Print ISSN: 0262-0898
Elektronische ISSN: 1573-7276
DOI
https://doi.org/10.1007/s10585-012-9482-4

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