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10.1038/cddis.2017.379

http://scihub22266oqcxt.onion/10.1038/cddis.2017.379
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C5680566!5680566!29048400
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suck abstract from ncbi


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pmid29048400      Cell+Death+Dis 2017 ; 8 (10): e3128-
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  • CD10?/ALDH? cells are the sole cisplatin-resistant component of a novel ovarian cancer stem cell hierarchy #MMPMID29048400
  • Ffrench B; Gasch C; Hokamp K; Spillane C; Blackshields G; Mahgoub TM; Bates M; Kehoe L; Mooney A; Doyle R; Doyle B; O'Donnell D; Gleeson N; Hennessy BT; Stordal B; O'Riain C; Lambkin H; O'Toole S; O'Leary JJ; Gallagher MF
  • Cell Death Dis 2017[Oct]; 8 (10): e3128- PMID29048400show ga
  • It is long established that tumour-initiating cancer stem cells (CSCs) possess chemoresistant properties. However, little is known of the mechanisms involved, particularly with respect to the organisation of CSCs as stem-progenitor-differentiated cell hierarchies. Here we aimed to elucidate the relationship between CSC hierarchies and chemoresistance in an ovarian cancer model. Using a single cell-based approach to CSC discovery and validation, we report a novel, four-component CSC hierarchy based around the markers cluster of differentiation 10 (CD10) and aldehyde dehydrogenase (ALDH). In a change to our understanding of CSC biology, resistance to chemotherapy drug cisplatin was found to be the sole property of CD10?/ALDH? CSCs, while all four CSC types were sensitive to chemotherapy drug paclitaxel. Cisplatin treatment quickly altered the hierarchy, resulting in a three-component hierarchy dominated by the cisplatin-resistant CD10?/ALDH? CSC. This organisation was found to be hard-wired in a long-term cisplatin-adapted model, where again CD10?/ALDH? CSCs were the sole cisplatin-resistant component, and all CSC types remained paclitaxel-sensitive. Molecular analysis indicated that cisplatin resistance is associated with inherent- and adaptive-specific drug efflux and DNA-damage repair mechanisms. Clinically, low CD10 expression was consistent with a specific set of ovarian cancer patient samples. Collectively, these data advance our understanding of the relationship between CSC hierarchies and chemoresistance, which was shown to be CSC- and drug-type specific, and facilitated by specific and synergistic inherent and adaptive mechanisms. Furthermore, our data indicate that primary stage targeting of CD10?/ALDH? CSCs in specific ovarian cancer patients in future may facilitate targeting of recurrent disease, before it ever develops.
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