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Selective Calcium Sensitivity in Immature Glioma Cancer Stem Cells

Wee, Shimei (författare)
Niklasson, Maria (författare)
Department of Medical Biochemistry and Biophysics, Karolinska Institutet
Marinescu, Voichita Dana (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
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Segerman, Anna (författare)
Uppsala universitet,Neuroonkologi
Schmidt, Linnea (författare)
Uppsala universitet,Neuroonkologi
Hermansson, Annika (författare)
Uppsala universitet,Neuroonkologi
Dirks, Peter (författare)
Forsberg-Nilsson, Karin (författare)
Uppsala universitet,Neuroonkologi
Westermark, Bengt (författare)
Uppsala universitet,Neuroonkologi
Uhrbom, Lene (författare)
Uppsala universitet,Neuroonkologi
Linnarsson, Sten (författare)
Karolinska Institutet
Nelander, Sven (författare)
Uppsala universitet,Neuroonkologi
Andang, Michael (författare)
Karolinska Institutet
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 (creator_code:org_t)
2014-12-22
2014
Engelska.
Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 9:12
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Tumor-initiating cells are a subpopulation in aggressive cancers that exhibit traits shared with stem cells, including the ability to self-renew and differentiate, commonly referred to as stemness. In addition, such cells are resistant to chemo- and radiation therapy posing a therapeutic challenge. To uncover stemness-associated functions in glioma-initiating cells (GICs), transcriptome profiles were compared to neural stem cells (NSCs) and gene ontology analysis identified an enrichment of Ca2+ signaling genes in NSCs and the more stem-like (NSC-proximal) GICs. Functional analysis in a set of different GIC lines regarding sensitivity to disturbed homeostasis using A23187 and Thapsigargin, revealed that NSC-proximal GICs were more sensitive, corroborating the transcriptome data. Furthermore, Ca2+ drug sensitivity was reduced in GICs after differentiation, with most potent effect in the NSC-proximal GIC, supporting a stemness-associated Ca2+ sensitivity. NSCs and the NSC-proximal GIC line expressed a larger number of ion channels permeable to potassium, sodium and Ca2+. Conversely, a higher number of and higher expression levels of Ca2+ binding genes that may buffer Ca2+, were expressed in NSC-distal GICs. In particular, expression of the AMPA glutamate receptor subunit GRIA1, was found to associate with Ca2+ sensitive NSC-proximal GICs, and decreased as GICs differentiated along with reduced Ca2+ drug sensitivity. The correlation between high expression of Ca2+ channels (such as GRIA1) and sensitivity to Ca2+ drugs was confirmed in an additional nine novel GIC lines. Calcium drug sensitivity also correlated with expression of the NSC markers nestin (NES) and FABP7 (BLBP, brain lipid-binding protein) in this extended analysis. In summary, NSC-associated NES+/FABP7(+)/GRIA1(+) GICs were selectively sensitive to disturbances in Ca2+ homeostasis, providing a potential target mechanism for eradication of an immature population of malignant cells.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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