Cancer Stem Cells in Glioblastoma Multiforme

被引:37
作者
Bradshaw, Amy [1 ]
Wickremesekera, Agadha [1 ,2 ]
Brasch, Helen D. [1 ]
Chibnall, Alice M. [1 ]
Davis, Paul F. [1 ]
Tan, Swee T. [1 ,3 ]
Itinteang, Tinte [1 ]
机构
[1] Gillies McIndoe Res Inst, Wellington, New Zealand
[2] Wellington Reg Hosp, Dept Neurosurg, Wellington, New Zealand
[3] Hutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
关键词
glioblastoma multiforme; embryonic; cancer; stem cells; expression; hierarchy;
D O I
10.3389/fsurg.2016.00048
中图分类号
R61 [外科手术学];
学科分类号
摘要
Aim: To identify and characterize cancer stem cells (CSC) in glioblastoma multiforme (GBM). Methods: Four -micrometer thick formalin-fixed paraffin-embedded GBM samples from six patients underwent 3,3-diaminobenzidine (DAB) and immunofluorescent (IF) immunohistochemical (IHC) staining for the embryonic stem cell (ESC) markers NANOG, OCT4, SALL4, SOX2, and pSTAT3. IF IHC staining was performed to demonstrate co-expression of these markers with GFAP. The protein expression and the transcriptional activities of the genes encoding NANOG, OCT4, SOX2, SALL4, and STAT3 were investigated using Western blotting (WB) and NanoString gene expression analysis, respectively. Results: DAB and IF IHC staining demonstrated the presence of a CSC population expressing NANOG, OCT4, SOX2, SALL4, and pSTAT3 with the almost ubiquitous presence of SOX2 and a relatively low abundance of OCT4, within GBM. The expression of NANOG, SOX2 and, pSTAT3 but, not OCT and SALL4, was confirmed by WB. NanoString gene analysis demonstrated transcriptional activation of NANOG, OCT4, SALL4, STAT3, and SOX2 in GBM. Conclusion: This study demonstrated a population of CSCs within GBM characterized by the expression of the CSC markers NANOG, SALL4, SOX2, pSTAT3 and OCT4 at the protein and mRNA levels. The almost ubiquitous presence of SOX2 and a relatively low abundance of OCT4 would support the putative existence of a stem cell hierarchy within GBM.
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页数:8
相关论文
共 42 条
[1]   Is tumor growth sustained by rare cancer stem cells or dominant clones? [J].
Adams, Jerry M. ;
Strasser, Andreas .
CANCER RESEARCH, 2008, 68 (11) :4018-4021
[2]  
Annovazzi L, 2011, CANCER GENOM PROTEOM, V8, P139
[3]   Core transcriptional regulatory circuitry in human embryonic stem cells [J].
Boyer, LA ;
Lee, TI ;
Cole, MF ;
Johnstone, SE ;
Levine, SS ;
Zucker, JR ;
Guenther, MG ;
Kumar, RM ;
Murray, HL ;
Jenner, RG ;
Gifford, DK ;
Melton, DA ;
Jaenisch, R ;
Young, RA .
CELL, 2005, 122 (06) :947-956
[4]   Cancer Stem Cell Hierarchy in Glioblastoma Multiforme [J].
Bradshaw, Amy ;
Wickremsekera, Agadha ;
Tan, Swee T. ;
Peng, Lifeng ;
Davis, Paul F. ;
Itinteang, Tinte .
FRONTIERS IN SURGERY, 2016, 3
[5]   Post-translational modulation of pluripotency [J].
Cai, Ning ;
Li, Mo ;
Qu, Jing ;
Liu, Guang-Hui ;
Izpisua Belmonte, Juan Carlos .
JOURNAL OF MOLECULAR CELL BIOLOGY, 2012, 4 (04) :262-265
[6]   Alternative Splicing Produces Nanog Protein Variants with Different Capacities for Self-renewal and Pluripotency in Embryonic Stem Cells [J].
Das, Satyabrata ;
Jena, Snehalata ;
Levasseur, Dana N. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (49) :42690-42703
[7]   A study of embryonic stem cell-related proteins in human astrocytomas: Identification of Nanog as a predictor of survival [J].
Elsir, Tamador ;
Edqvist, Per-Henrik ;
Carlson, Joseph ;
Ribom, Dan ;
Bergqvist, Michael ;
Ekman, Simon ;
Popova, Svetlana N. ;
Alafuzoff, Irina ;
Ponten, Fredrik ;
Nister, Monica ;
Smits, Anja .
INTERNATIONAL JOURNAL OF CANCER, 2014, 134 (05) :1123-1131
[8]   ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS [J].
EVANS, MJ ;
KAUFMAN, MH .
NATURE, 1981, 292 (5819) :154-156
[9]   Frontiers in targeting glioma stem cells [J].
Frosina, Guido .
EUROPEAN JOURNAL OF CANCER, 2011, 47 (04) :496-507
[10]   The Bright and the Dark Sides of DNA Repair in Stem Cells [J].
Frosina, Guido .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2010,