دورية أكاديمية

Contributions to drug resistance in glioblastoma derived from malignant cells in the sub-ependymal zone.

التفاصيل البيبلوغرافية
العنوان: Contributions to drug resistance in glioblastoma derived from malignant cells in the sub-ependymal zone.
المؤلفون: Piccirillo SG; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK., Spiteri I; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Cambridge, UK., Sottoriva A; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Cambridge, UK.; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, USA., Touloumis A; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Cambridge, UK.; European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridge, UK., Ber S; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK., Price SJ; Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK., Heywood R; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK., Francis NJ; Department of Oncology and the Medical Research Council Cancer Cell Unit, Hutchison/MRC Research Centre, Cambridge, UK., Howarth KD; Hutchison/MRC Research Centre and Department of Pathology, University of Cambridge, Cambridge, UK., Collins VP; Division of Molecular Histopathology, Department of Pathology, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK., Venkitaraman AR; Department of Oncology and the Medical Research Council Cancer Cell Unit, Hutchison/MRC Research Centre, Cambridge, UK., Curtis C; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, USA., Marioni JC; European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridge, UK., Tavaré S; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Cambridge, UK., Watts C; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
المصدر: Cancer research [Cancer Res] 2015 Jan 01; Vol. 75 (1), pp. 194-202. Date of Electronic Publication: 2014 Nov 18.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: American Association for Cancer Research Country of Publication: United States NLM ID: 2984705R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1538-7445 (Electronic) Linking ISSN: 00085472 NLM ISO Abbreviation: Cancer Res Subsets: MEDLINE
أسماء مطبوعة: Publication: Baltimore, Md. : American Association for Cancer Research
Original Publication: Chicago [etc.]
مواضيع طبية MeSH: Brain Neoplasms/*drug therapy , Brain Neoplasms/*pathology , Ependyma/*pathology , Glioblastoma/*drug therapy , Glioblastoma/*pathology , Neoplastic Stem Cells/*pathology , Neural Stem Cells/*pathology, Cell Line, Tumor ; Drug Resistance, Neoplasm ; Humans
مستخلص: Glioblastoma, the most common and aggressive adult brain tumor, is characterized by extreme phenotypic diversity and treatment failure. Through fluorescence-guided resection, we identified fluorescent tissue in the sub-ependymal zone (SEZ) of patients with glioblastoma. Histologic analysis and genomic characterization revealed that the SEZ harbors malignant cells with tumor-initiating capacity, analogous to cells isolated from the fluorescent tumor mass (T). We observed resistance to supramaximal chemotherapy doses along with differential patterns of drug response between T and SEZ in the same tumor. Our results reveal novel insights into glioblastoma growth dynamics, with implications for understanding and limiting treatment resistance.
(©2014 American Association for Cancer Research.)
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معلومات مُعتمدة: 16700 United Kingdom CRUK_ Cancer Research UK; A14545 United Kingdom CRUK_ Cancer Research UK; C14303/A10825 United Kingdom CRUK_ Cancer Research UK; C1023/A14545 United Kingdom CRUK_ Cancer Research UK; NIHR/CS/009/011 United Kingdom DH_ Department of Health; A10825 United Kingdom CRUK_ Cancer Research UK; 14545 United Kingdom CRUK_ Cancer Research UK; MC_UU_12022/1 United Kingdom MRC_ Medical Research Council; 090340 United Kingdom WT_ Wellcome Trust; G1001522 United Kingdom MRC_ Medical Research Council
فهرسة مساهمة: Indexing Agency: NLM Local ID #: EMS61174.
تواريخ الأحداث: Date Created: 20141120 Date Completed: 20150423 Latest Revision: 20240210
رمز التحديث: 20240210
مُعرف محوري في PubMed: PMC4286248
DOI: 10.1158/0008-5472.CAN-13-3131
PMID: 25406193
قاعدة البيانات: MEDLINE
الوصف
تدمد:1538-7445
DOI:10.1158/0008-5472.CAN-13-3131