Microarray analysis of tumour antigen expression in presentation acute myeloid leukaemia
Microarray analysis of tumour antigen expression in presentation acute myeloid leukaemia
Acute myeloid leukaemia (AML) is a difficult to treat disease, especially for those patients who have no eligible haematopoietic stem cells (HSC) donor. One of the most promising treatment options for these patients is immunotherapy. To investigate the expression of known tumour antigens in AML, we analysed cDNA microarray data from 124 presentation AML patient samples and investigated the present/absent calls of 82 tumour-specific or -associated antigens. We found 11 antigens which were expressed in AML patient samples but not normal donors. Nine of these were cancer-testis (CT) antigens, previously shown to be expressed in tumour cells and immunologically protected sites and at very low levels, if at all, in normal tissues. Expression was confirmed using real-time PCR. We have identified a number of CT antigens with expression in presentation AML samples but not normal donor samples, which may provide effective targets for future immunotherapy treatments early in disease
cDNA microarray, cancer-testis antigens, acute myeloid leukaemia, RAGE1, FLT3
703-713
Guinn, Barbara-ann
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Gilkes, Amanda F.
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Woodward, Eleanor
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Westwood, Nigel B.
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Mufti, Ghulam J.
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Linch, David
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Burnett, Alan K.
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Mills, Ken I.
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5 August 2005
Guinn, Barbara-ann
728d28c9-a23d-413a-ba1d-4531005705d7
Gilkes, Amanda F.
ed9d4246-50b3-465a-aff3-bcd693f5e508
Woodward, Eleanor
47176980-fa8e-432d-b1ff-d2bb5855f9fa
Westwood, Nigel B.
cbe7bf7f-6ac4-4422-88a3-8c28b65f517c
Mufti, Ghulam J.
940de420-bc41-4006-8517-f2c926ba70aa
Linch, David
0ac602f1-c036-40aa-b554-d8a204abe425
Burnett, Alan K.
50a1c448-e723-4da8-9b36-5074383e66de
Mills, Ken I.
be9c4b93-fda3-40b1-8514-9191652ab8b7
Guinn, Barbara-ann, Gilkes, Amanda F., Woodward, Eleanor, Westwood, Nigel B., Mufti, Ghulam J., Linch, David, Burnett, Alan K. and Mills, Ken I.
(2005)
Microarray analysis of tumour antigen expression in presentation acute myeloid leukaemia.
Biochemical and Biophysical Research Communications, 333 (3), .
(doi:10.1016/j.bbrc.2005.05.161).
Abstract
Acute myeloid leukaemia (AML) is a difficult to treat disease, especially for those patients who have no eligible haematopoietic stem cells (HSC) donor. One of the most promising treatment options for these patients is immunotherapy. To investigate the expression of known tumour antigens in AML, we analysed cDNA microarray data from 124 presentation AML patient samples and investigated the present/absent calls of 82 tumour-specific or -associated antigens. We found 11 antigens which were expressed in AML patient samples but not normal donors. Nine of these were cancer-testis (CT) antigens, previously shown to be expressed in tumour cells and immunologically protected sites and at very low levels, if at all, in normal tissues. Expression was confirmed using real-time PCR. We have identified a number of CT antigens with expression in presentation AML samples but not normal donor samples, which may provide effective targets for future immunotherapy treatments early in disease
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Published date: 5 August 2005
Keywords:
cDNA microarray, cancer-testis antigens, acute myeloid leukaemia, RAGE1, FLT3
Identifiers
Local EPrints ID: 71575
URI: http://eprints.soton.ac.uk/id/eprint/71575
ISSN: 0006-291X
PURE UUID: 3d2e149e-cedb-4c0f-83a8-e04868075c21
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Date deposited: 14 Dec 2009
Last modified: 13 Mar 2024 20:33
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Contributors
Author:
Barbara-ann Guinn
Author:
Amanda F. Gilkes
Author:
Eleanor Woodward
Author:
Nigel B. Westwood
Author:
Ghulam J. Mufti
Author:
David Linch
Author:
Alan K. Burnett
Author:
Ken I. Mills
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