ALDH1+ cancer stem cells in epithelial ovarian cancer are associated with chemoresistance and poor survival

2014 ◽  
Vol 74 (S 01) ◽  
Author(s):  
K Kübler ◽  
MD Keyver-Paik ◽  
M Debald ◽  
B Rostamzadeh ◽  
T Thiesler ◽  
...  
Oncotarget ◽  
2014 ◽  
Vol 5 (12) ◽  
pp. 4305-4319 ◽  
Author(s):  
Anna Pastò ◽  
Chiara Bellio ◽  
Giorgia Pilotto ◽  
Vincenzo Ciminale ◽  
Micol Silic-Benussi ◽  
...  

2010 ◽  
Vol 2010 ◽  
pp. 1-9 ◽  
Author(s):  
Sheetal Dyall ◽  
Simon A. Gayther ◽  
Dimitra Dafou

The cancer stem cell hypothesis is becoming more widely accepted as a model for carcinogenesis. Tumours are heterogeneous both at the molecular and cellular level, containing a small population of cells that possess highly tumourigenic “stem-cell” properties. Cancer stem cells (CSCs), or tumour-initiating cells, have the ability to self-renew, generate xenografts reminiscent of the primary tumour that they were derived from, and are chemoresistant. The characterisation of the CSC population within a tumour that drives its growth could provide novel target therapeutics against these cells specifically, eradicating the cancer completely. There have been several reports describing the isolation of putative cancer stem cell populations in several cancers; however, no defined set of markers has been identified that conclusively characterises “stem-like” cancer cells. This paper highlights the current experimental approaches that have been used in the field and discusses their limitations, with specific emphasis on the identification and characterisation of the CSC population in epithelial ovarian cancer.


2011 ◽  
Author(s):  
Gang Yin ◽  
Vinny Craveiro ◽  
Jennie Holmberg ◽  
Han-Hsuan Fu ◽  
Michael K. Montagna ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-12 ◽  
Author(s):  
Karina Dahl Steffensen ◽  
Ayesha B. Alvero ◽  
Yang Yang ◽  
Marianne Waldstrøm ◽  
Pei Hui ◽  
...  

Epithelial ovarian cancer stem cells (EOC stem cells) have been associated with recurrence and chemoresistance. CD44 and CK18 are highly expressed in cancer stem cells and function as tools for their identification and characterization. We investigated the association between the number of CD44+ EOC stem cells in ovarian cancer tumors and progression-free survival. EOC stem cells exist as clusters located close to the stroma forming the cancer stem cell “niche”. 17.1% of the samples reveled high number of CD44+ EOC stem cells (>20% positive cells). In addition, the number of CD44+ EOC stem cells was significantly higher in patients with early-stage ovarian cancer (FIGO I/II), and it was associated with shorter progression-free survival (P=0.026). This study suggests that quantification of the number of EOC stem cells in the tumor can be used as a predictor of disease and could be applied for treatment selection in early-stage ovarian cancer.


Cell Cycle ◽  
2011 ◽  
Vol 10 (13) ◽  
pp. 2206-2214 ◽  
Author(s):  
Ilana Chefetz ◽  
Jennie C. Holmberg ◽  
Ayesha B. Alvero ◽  
Irene Visintin ◽  
Gil Mor

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