Label-free quantitative proteomics unravels the importance of RNA processing in glioma malignancy. (20th May 2017)
- Record Type:
- Journal Article
- Title:
- Label-free quantitative proteomics unravels the importance of RNA processing in glioma malignancy. (20th May 2017)
- Main Title:
- Label-free quantitative proteomics unravels the importance of RNA processing in glioma malignancy
- Authors:
- Bi, Baibin
Li, Feng
Guo, Jisheng
Li, Cuiling
Jing, Ruirui
Lv, Xin
Chen, Xinjun
Wang, Fengqin
Azadzoi, Kazem M.
Wang, Lin
Liu, Yuguang
Yang, Jing-Hua - Abstract:
- Highlights: Quantitative proteomics on different grades of glioma was performed. A list of differentially expressed proteins was identified. Importance of RNA processing in glioma malignancy was revealed. RNA processing links with crucial signal transduction and neuronal function and activity. Representative proteins were validated by immune assay. Abstract: Glioma, one of the most common cancers in human, is classified to different grades according to the degrees of malignancy. Glioblastoma (GBM) is known to be the most malignant (Grade IV) whereas low-grade astrocytoma (LGA, Grade II) is relatively benign. The mechanism underlying the pathogenesis and progression of glioma malignancy remains unclear. Here we report a quantitative proteomic study to elucidate the differences between GBM and LGA using liquid chromatography and tandem mass spectrometry followed by label-free quantification. A total of 136 proteins were differentially expressed in GBM for at least five folds in comparison with LGA. Ontological analysis revealed a close correlation between GBM-associated proteins and RNA processing. Interaction network analysis indicated that the GBM-associated proteins in the RNA processing were linked to crucial signaling transduction modulators including epidermal growth factor receptor (EGFR), signal transducer and activator of transcription 1 (STAT1), and mitogen-activated protein kinase 1 (MAPK1), which were further connected to the proteins important for neuronalHighlights: Quantitative proteomics on different grades of glioma was performed. A list of differentially expressed proteins was identified. Importance of RNA processing in glioma malignancy was revealed. RNA processing links with crucial signal transduction and neuronal function and activity. Representative proteins were validated by immune assay. Abstract: Glioma, one of the most common cancers in human, is classified to different grades according to the degrees of malignancy. Glioblastoma (GBM) is known to be the most malignant (Grade IV) whereas low-grade astrocytoma (LGA, Grade II) is relatively benign. The mechanism underlying the pathogenesis and progression of glioma malignancy remains unclear. Here we report a quantitative proteomic study to elucidate the differences between GBM and LGA using liquid chromatography and tandem mass spectrometry followed by label-free quantification. A total of 136 proteins were differentially expressed in GBM for at least five folds in comparison with LGA. Ontological analysis revealed a close correlation between GBM-associated proteins and RNA processing. Interaction network analysis indicated that the GBM-associated proteins in the RNA processing were linked to crucial signaling transduction modulators including epidermal growth factor receptor (EGFR), signal transducer and activator of transcription 1 (STAT1), and mitogen-activated protein kinase 1 (MAPK1), which were further connected to the proteins important for neuronal structural integrity, development and functions. Upregulation of 40S ribosomal protein S5 (RPS5), Ferritin Heavy chain (FTH1) and STAT1, and downregulation of tenascin R (TNR) were validated as representatives by immune assays. In summary, we revealed a panel of GBM-associated proteins and the important modulators centered at the RNA-processing network in glioma malignancy that may become novel biomarkers and help elucidate the underlying mechanism. … (more)
- Is Part Of:
- Neuroscience. Volume 351(2017)
- Journal:
- Neuroscience
- Issue:
- Volume 351(2017)
- Issue Display:
- Volume 351, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 351
- Issue:
- 2017
- Issue Sort Value:
- 2017-0351-2017-0000
- Page Start:
- 84
- Page End:
- 95
- Publication Date:
- 2017-05-20
- Subjects:
- 1PRPF8 pre-mRNA splicing factor 8 -- AGRN agrin -- DTT dithiothreitol -- EGFR epidermal growth factor receptor -- FDR false discovery rate -- FGF1 Fibroblast Growth Factor 1 -- FTH1 Ferritin Heavy chain -- GBM glioblastoma -- HPLC high-pressure liquid chromatography -- KEGG Kyoto Encyclopedia of Genes and Genomes database -- LAMC1 laminin gamma -- LC-MS/MS liquid chromatography tandem mass spectrometry -- LGA low-grade astrocytoma -- MALDI-TOF matrix-assisted laser desorption/ionization time of flight mass spectrometry -- MAPK1 mitogen-activated protein kinase 1 -- NCAN neurocan -- NCL nucleolin -- RAB3A Ras-related protein Rab-3A -- RPL15 ribosomal protein L15 -- RPS5 40S ribosomal protein S5 -- SF3B2 Splicing factor 3B subunit 2 -- SNCA synuclein alphaSYN1:synapsin I -- STAT1 signal transducer and activator of transcription 1 -- STRING Search Tool for the Retrieval of Interacting Genes -- SYT1 synaptotagmin I -- TNR tenascin R -- WHO World Health Organization
cancer biomarker(s) -- cancer pathogenesis -- glioblastoma -- label-free quantification -- mass spectrometry
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
Electronic journals
Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2017.03.023 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.559000
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