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Large Scale Identification of Variant Proteins in Glioma Stem Cells

Mostovenko, Ekaterina (author)
Virginia Commonwealth University
Végvári, Ákos (author)
Lund University,Lunds universitet,Clinical Protein Science and Imaging,Forskargrupper vid Lunds universitet,Lund University Research Groups
Rezeli, Melinda (author)
Lund University,Lunds universitet,Clinical Protein Science and Imaging,Forskargrupper vid Lunds universitet,Lund University Research Groups
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Lichti, Cheryl F. (author)
Virginia Commonwealth University,Washington University in St. Louis
Fenyö, David (author)
New York University
Wang, Qianghu (author)
University of Texas
Lang, Frederick F. (author)
University of Texas
Sulman, Erik P. (author)
University of Texas
Sahlin, K. Barbara (author)
Lund University,Lunds universitet,Clinical Protein Science and Imaging,Forskargrupper vid Lunds universitet,Lund University Research Groups
Marko-Varga, György (author)
Lund University,Lunds universitet,Clinical Protein Science and Imaging,Forskargrupper vid Lunds universitet,Lund University Research Groups
Nilsson, Carol L. (author)
Lund University,Lunds universitet,Masspektrometri,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Mass Spectrometry,Section V,Department of Clinical Sciences, Lund,Faculty of Medicine
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 (creator_code:org_t)
2017-12-21
2018
English 7 s.
In: ACS Chemical Neuroscience. - : American Chemical Society (ACS). - 1948-7193. ; 9:1, s. 73-79
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Glioblastoma (GBM), the most malignant of primary brain tumors, is a devastating and deadly disease, with a median survival of 14 months from diagnosis, despite standard regimens of radical brain tumor surgery, maximal safe radiation, and concomitant chemotherapy. GBM tumors nearly always re-emerge after initial treatment and frequently display resistance to current treatments. One theory that may explain GBM re-emergence is the existence of glioma stemlike cells (GSCs). We sought to identify variant protein features expressed in low passage GSCs derived from patient tumors. To this end, we developed a proteomic database that reflected variant and nonvariant sequences in the human proteome, and applied a novel retrograde proteomic workflow, to identify and validate the expression of 126 protein variants in 33 glioma stem cell strains. These newly identified proteins may harbor a subset of novel protein targets for future development of GBM therapy.

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 -- Läkemedelskemi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medicinal Chemistry (hsv//eng)

Keyword

bioinformatics
GBM
Glioblastoma
parallel reaction monitoring
precision medicine
protein quantification
protein single amino acid variants
proteomics
targeted mass spectrometry
transcriptomics

Publication and Content Type

art (subject category)
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