Literature DB >> 15963951

Microarray analysis of tumour antigen expression in presentation acute myeloid leukaemia.

Barbara-Ann Guinn1, Amanda F Gilkes, Eleanor Woodward, Nigel B Westwood, Ghulam J Mufti, David Linch, Alan K Burnett, Ken I Mills.   

Abstract

Acute myeloid leukaemia (AML) is a difficult to treat disease, especially for those patients who have no eligible haematopoietic stem cell (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 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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Year:  2005        PMID: 15963951     DOI: 10.1016/j.bbrc.2005.05.161

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  8 in total

1.  CD8(+) T-cell immunity against cancer-testis antigens develops following allogeneic stem cell transplantation and reveals a potential mechanism for the graft-versus-leukemia effect.

Authors:  Andrew McLarnon; Karen P Piper; Oliver C Goodyear; Julie M Arrazi; Premini Mahendra; Mark Cook; Fiona Clark; Guy Pratt; Charles Craddock; Paul A H Moss
Journal:  Haematologica       Date:  2010-05-11       Impact factor: 9.941

2.  MOK overexpression is associated with promoter hypomethylation in patients with acute myeloid leukemia.

Authors:  Jun Qian; Qin Chen; Dong-Ming Yao; Lei Yang; Jing Yang; Xiang-Mei Wen; Ying-Ying Zhang; Hai-Yan Chai; Ji-Chun Ma; Zhao-Qun Deng; Jiang Lin
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01

3.  An analogue peptide from the Cancer/Testis antigen PASD1 induces CD8+ T cell responses against naturally processed peptide.

Authors:  Nicola Hardwick; Sarah Buchan; Wendy Ingram; Ghazala Khan; Gisella Vittes; Jason Rice; Karen Pulford; Ghulam Mufti; Freda Stevenson; Barbara-ann Guinn
Journal:  Cancer Immun       Date:  2013-07-15

4.  Leukemia associated antigens: their dual role as biomarkers and immunotherapeutic targets for acute myeloid leukemia.

Authors:  Barbara-Ann Guinn; Azim Mohamedali; Ken I Mills; Barbara Czepulkowski; Michael Schmitt; Jochen Greiner
Journal:  Biomark Insights       Date:  2007-02-14

5.  Genes overexpressed in different human solid cancers exhibit different tissue-specific expression profiles.

Authors:  Jacob Bock Axelsen; Jacob Bock-Axelsen; Joseph Lotem; Leo Sachs; Eytan Domany
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-30       Impact factor: 11.205

6.  Restriction of GAGE protein expression to subpopulations of cancer cells is independent of genotype and may limit the use of GAGE proteins as targets for cancer immunotherapy.

Authors:  M F Gjerstorff; L E Johansen; O Nielsen; K Kock; H J Ditzel
Journal:  Br J Cancer       Date:  2006-06-19       Impact factor: 7.640

Review 7.  The Role of Cell Division Autoantigen 1 (CDA1) in Renal Fibrosis of Diabetic Nephropathy.

Authors:  LinLin Chen; Jiao Wu; Bin Hu; Changbai Liu; Hu Wang
Journal:  Biomed Res Int       Date:  2021-04-28       Impact factor: 3.411

8.  Expression of putative targets of immunotherapy in acute myeloid leukemia and healthy tissues.

Authors:  M Goswami; N Hensel; B D Smith; G T Prince; L Qin; H I Levitsky; S A Strickland; M Jagasia; B N Savani; J W Fraser; H Sadrzadeh; T Rajkhowa; S Ito; N A Jain; M Battiwalla; A T Fathi; M J Levis; A J Barrett; C S Hourigan
Journal:  Leukemia       Date:  2014-01-10       Impact factor: 11.528

  8 in total

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