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PTPN6 expression is epigenetically regulated and influences survival and response to chemotherapy in high-grade gliomas

Sooman, Linda (author)
Uppsala universitet,Enheten för onkologi
Ekman, Simon (author)
Uppsala universitet,Enheten för onkologi
Tsakonas, Georgios (author)
Uppsala universitet,Enheten för onkologi
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Jaiswal, Archita (author)
Navani, Sanjay (author)
Edqvist, Per-Henrik (author)
Uppsala universitet,Molekylär och morfologisk patologi,Science for Life Laboratory, SciLifeLab
Pontén, Fredrik (author)
Uppsala universitet,Molekylär och morfologisk patologi,Science for Life Laboratory, SciLifeLab
Bergström, Stefan (author)
Uppsala universitet,Enheten för onkologi
Johansson, Mikael (author)
Umeå universitet,Institutionen för strålningsvetenskaper
Wu, Xuping (author)
Uppsala universitet,Enheten för onkologi
Blomquist, Erik (author)
Uppsala universitet,Enheten för onkologi
Bergqvist, Michael (author)
Uppsala universitet,Enheten för onkologi
Gullbo, Joachim (author)
Uppsala universitet,Enheten för onkologi,Cancerfarmakologi och beräkningsmedicin
Lennartsson, Johan (author)
Uppsala universitet,Ludwiginstitutet för cancerforskning
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 (creator_code:org_t)
2014-02-09
2014
English.
In: Tumor Biology. - : Springer Science and Business Media LLC. - 1010-4283 .- 1423-0380. ; 35:5, s. 4479-4488
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The prognosis of high-grade glioma patients is poor, and the tumors are characterized by resistance to therapy. The aims of this study were to analyze the prognostic value of the expression of the protein tyrosine phosphatase non-receptor type 6 (PTPN6, also referred to as SHP1) in high-grade glioma patients, the epigenetic regulation of the expression of PTPN6, and the role of its expression in chemotherapy resistance in glioma-derived cells. PTPN6 expression was analyzed with immunohistochemistry in 89 high-grade glioma patients. Correlation between PTPN6 expression and overall survival was analyzed with Kaplan-Meier univariate analysis and Cox regression multivariate analysis. Differences in drug sensitivity to a panel of 16 chemotherapeutic drugs between PTPN6-overexpressing clones and control clones were analyzed in vitro with the fluorometric microculture cytotoxicity assay. Cell cycle analysis was done with Krishan staining and flow cytometry. Apoptosis was analyzed with a cell death detection ELISA kit as well as cleaved caspase-3 and caspase-9 Western blotting. Autophagy was analyzed with LC3B Western blotting. Methylation of the PTPN6 promoter was analyzed with bisulfite pyrosequencing, and demethylation of PTPN6 was done with decitabine treatment. The PTPN6 expression correlated in univariate analysis to poor survival for anaplastic glioma patients (p = 0.026). In glioma-derived cell lines, overexpression of PTPN6 caused increase resistance (p < 0.05) to the chemotherapeutic drugs bortezomib, cisplatin, and melphalan. PTPN6 expression did not affect bortezomib-induced cell cycle arrest, apoptosis, or autophagy. Low PTPN6 promoter methylation correlated to protein expression, and the protein expression was increased upon demethylation in glioma-derived cells. PTPN6 expression may be a factor contributing to poor survival for anaplastic glioma patients, and in glioma-derived cells, its expression is epigenetically regulated and influences the response to chemotherapy.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

High-grade glioma
PTPN6
SHP1
Survival
Chemotherapy
Methylation

Publication and Content Type

ref (subject category)
art (subject category)

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