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

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, co...

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Main Authors: Patel, S, Chen, H, Monti, L, Gould, E, Haralambieva, E, Schmid, J, Toomey, D, Woessmann, W, Roncador, G, Hatton, C, Liggins, A, Taramelli, R, Banham, A, Acquati, F, Murphy, D, Pulford, K
Format: Journal article
Language:English
Published: 2012
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author Patel, S
Chen, H
Monti, L
Gould, E
Haralambieva, E
Schmid, J
Toomey, D
Woessmann, W
Roncador, G
Hatton, C
Liggins, A
Taramelli, R
Banham, A
Acquati, F
Murphy, D
Pulford, K
author_facet Patel, S
Chen, H
Monti, L
Gould, E
Haralambieva, E
Schmid, J
Toomey, D
Woessmann, W
Roncador, G
Hatton, C
Liggins, A
Taramelli, R
Banham, A
Acquati, F
Murphy, D
Pulford, K
author_sort Patel, S
collection OXFORD
description 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.
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spelling oxford-uuid:82228c9f-6003-4788-901d-493cf9bf86962022-03-26T21:35:14ZRNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:82228c9f-6003-4788-901d-493cf9bf8696EnglishSymplectic Elements at Oxford2012Patel, SChen, HMonti, LGould, EHaralambieva, ESchmid, JToomey, DWoessmann, WRoncador, GHatton, CLiggins, ATaramelli, RBanham, AAcquati, FMurphy, DPulford, KCharacterising 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.
spellingShingle Patel, S
Chen, H
Monti, L
Gould, E
Haralambieva, E
Schmid, J
Toomey, D
Woessmann, W
Roncador, G
Hatton, C
Liggins, A
Taramelli, R
Banham, A
Acquati, F
Murphy, D
Pulford, K
RNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.
title RNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.
title_full RNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.
title_fullStr RNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.
title_full_unstemmed RNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.
title_short RNASET2--an autoantigen in anaplastic large cell lymphoma identified by protein array analysis.
title_sort rnaset2 an autoantigen in anaplastic large cell lymphoma identified by protein array analysis
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