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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by mollevi
Last modified by jacques.colinge
Group name EquipeJC
Item Type Journal Article
Title Comprehensive comparative and semiquantitative proteome of a very low number of native and matched epstein-barr-virus-transformed B lymphocytes infiltrating human melanoma
Creator Maurer et al.
Author M. Maurer
Author A. C. Muller
Author K. Parapatics
Author W. F. Pickl
Author C. Wagner
Author E. L. Rudashevskaya
Author F. P. Breitwieser
Author J. Colinge
Author K. Garg
Author J. Griss
Author K. L. Bennett
Author S. N. Wagner
Abstract Melanoma, the deadliest form of skin cancer, is highly immunogenic and frequently infiltrated with immune cells including B cells. The role of tumor-infiltrating B cells (TIBCs) in melanoma is as yet unresolved, possibly due to technical challenges in obtaining TIBCs in sufficient quantity for extensive studies and due to the limited life span of B cells in vitro. A comprehensive workflow has thus been developed for successful isolation and proteomic analysis of a low number of TIBCs from fresh, human melanoma tissue. In addition, we generated in vitro-proliferating TIBC cultures using simultaneous stimulation with Epstein-Barr virus (EBV) and the TLR9 ligand CpG-oligodesoxynucleotide (CpG ODN). The FASP method and iTRAQ labeling were utilized to obtain a comparative, semiquantitative proteome to assess EBV-induced changes in TIBCs. By using as few as 100 000 B cells ( approximately 5 mug protein)/sample for our proteomic study, a total number of 6507 proteins were identified. EBV-induced changes in TIBCs are similar to those already reported for peripheral B cells and largely involve changes in cell cycle proliferation, apoptosis, and interferon response, while most of the proteins were not significantly altered. This study provides an essential, further step toward detailed characterization of TIBCs including functional in vitro analysis.
Publication J Proteome Res
Volume 13
Pages 2830-45
Date Jun 6 2014
Journal Abbr Journal of proteome research
DOI 10.1021/pr401270y
ISSN 1535-3907 (Electronic) 1535-3893 (Linking)
Tags B-Lymphocytes/*metabolism/virology, Cell Proliferation, Cell Separation, Gene Expression, Gene Expression Regulation, Neoplastic, Gene Ontology, Herpesvirus 4, Human/*physiology, Humans, Melanoma/*immunology/pathology/secondary, Molecular Sequence Annotation, original, phd, Proteome/genetics/*metabolism, RNA, Messenger/genetics/metabolism, Tumor Cells, Cultured
Date Added 2018/11/14 - 11:48:35
Date Modified 2019/10/22 - 21:19:47
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