Literature DB >> 22732457

RNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.

Suketu Patel1, Hong Chen, Laura Monti, Edith Gould, Eugenia Haralambieva, Jasmin Schmid, David Toomey, Wilhelm Woessmann, Giovanna Roncador, Chris S R Hatton, Amanda P Liggins, Roberto Taramelli, Alison H Banham, Francesco Acquati, Derek Murphy, Karen Pulford.   

Abstract

Characterising tumour-associated antigens (TAAs) not only represents an important approach to the identification of new diagnostic/prognostic markers, but can also provide information on disease processes and additional potential therapeutic targets. Preliminary screening of a protein macroarray, containing more than 12,000 different proteins, with sera from anaplastic lymphoma kinase (ALK)-negative and ALK-positive anaplastic large cell lymphoma (ALCL) patients identified ribonuclease and tumour suppressor protein Ribonuclease T2 (RNASET2), phosphatase lipid phosphate phosphatase-related protein type 3 (LPPR3) and apoptotic adaptor molecule Fas-associating protein (FADD) as ALK-negative ALCL-associated TAAs. Further validation of these observations was confirmed using the ALCL sera in reverse ELISAs. The circulating anti-RNASET2 autoantibodies present in ALCL patients' sera also recognised eukaryotically expressed RNASET2 protein. RNASET2 expression was then investigated in normal tissues and in lymphomas to explore its clinical potential. RNASET2 protein and mRNA levels showed highest expression in the spleen, leucocytes and pancreas. RNASET2 protein expression was not restricted to ALK-negative ALCL (81%), being expressed in ALK-positive ALCL (65%) as well as in a number of other lymphomas. The immunological recognition of RNASET2, its expression in ALCL and other lymphomas together with its known tumourigenic properties suggest that further studies on this autoantigen are warranted. Crown
Copyright © 2012. Published by Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22732457     DOI: 10.1016/j.jprot.2012.06.009

Source DB:  PubMed          Journal:  J Proteomics        ISSN: 1874-3919            Impact factor:   4.044


  4 in total

1.  RNASET2, GPR174, and PTPN22 gene polymorphisms are related to the risk of liver damage associated with the hyperthyroidism in patients with Graves' disease.

Authors:  Qing Zhang; Shaozheng Liu; Yanxing Guan; Qingjie Chen; Qing Zhang; Xiang Min
Journal:  J Clin Lab Anal       Date:  2017-05-31       Impact factor: 2.352

2.  Loss of function of Ribonuclease T2, an ancient and phylogenetically conserved RNase, plays a crucial role in ovarian tumorigenesis.

Authors:  Francesco Acquati; Marta Lualdi; Sabrina Bertilaccio; Laura Monti; Giovanna Turconi; Marco Fabbri; Annalisa Grimaldi; Achille Anselmo; Antonio Inforzato; Angelo Collotta; Laura Cimetti; Cristina Riva; Laura Gribaldo; Paolo Ghia; Roberto Taramelli
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-29       Impact factor: 11.205

3.  Increased Expression of Phosphorylated FADD in Anaplastic Large Cell and Other T-Cell Lymphomas.

Authors:  Suketu Patel; Derek Murphy; Eugenia Haralambieva; Zainalabideen A Abdulla; Kah Keng Wong; Hong Chen; Edith Gould; Giovanna Roncador; Chris Hatton; Amanda P Anderson; Alison H Banham; Karen Pulford
Journal:  Biomark Insights       Date:  2014-09-03

4.  FBXO6-mediated RNASET2 ubiquitination and degradation governs the development of ovarian cancer.

Authors:  Mei Ji; Zhao Zhao; Yue Li; Penglin Xu; Jia Shi; Zhe Li; Kaige Wang; Xiaotian Huang; Bin Liu
Journal:  Cell Death Dis       Date:  2021-03-25       Impact factor: 8.469

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.