Literature DB >> 26464715

Rates of MAGE-A3 and PRAME expressing tumors in FFPE tissue specimens from bladder cancer patients: potential targets for antigen-specific cancer immunotherapeutics.

Evelyne Lerut1, Hendrik Van Poppel2, Steven Joniau2, Olivier Gruselle3, Thierry Coche3, Patrick Therasse4.   

Abstract

INTRODUCTION: Antigen-specific active immunotherapy is an investigational therapeutic approach of potential interest for bladder cancer regardless of disease stage. Clinical development of antigen-specific immunotherapeutics against bladder cancer must be preceded by assessment of the expression of relevant genes in bladder tumors. The objectives of this study (NCT01706185) were to assess the rate of expression of the MAGE-A3 and PRAME genes in bladder tumors and to investigate the feasibility of using formalin-fixed paraffin-embedded (FFPE) tumor tissues for testing.
MATERIALS AND METHODS: Archived FFPE bladder tumor specimens (any stage) were tested for mRNA expression of MAGE-A3 and PRAME using antigen-specific quantitative reverse transcription polymerase chain reaction assays. Data on patients and tumor characteristics were obtained from hospital records to investigate these characteristics' possible association with the antigen expression.
RESULTS: Over 92% of the 156 tumors examined gave valid antigen test results. Of the tumors with a valid test, 46.5% were MAGE-A3-positive, 32.2% were PRAME-positive and 59.7% positive for at least one of them. Exploratory analyses of possible associations between antigen expression and patient or tumor characteristics did not identify clear associations between antigen expression and any of the variables investigated.
CONCLUSIONS: Assessment of tumor antigen mRNA expression by using FFPE bladder tissues was feasible. The rates of MAGE-A3-positive and PRAME-positive tumors indicate that both antigens may be interesting targets for immunotherapeutics against bladder cancer.

Entities:  

Keywords:  Bladder cancer; FFPE samples; MAGE-A3 antigen; PRAME antigen; cancer immunotherapeutics

Mesh:

Substances:

Year:  2015        PMID: 26464715      PMCID: PMC4583947     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  40 in total

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Journal:  J Immunother       Date:  2011-09       Impact factor: 4.456

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Authors:  Adalberto Costessi; Nawel Mahrour; Esther Tijchon; Rieka Stunnenberg; Marieke A Stoel; Pascal W Jansen; Dotan Sela; Skylar Martin-Brown; Michael P Washburn; Laurence Florens; Joan W Conaway; Ronald C Conaway; Hendrik G Stunnenberg
Journal:  EMBO J       Date:  2011-08-05       Impact factor: 11.598

4.  Expression of the MAGE-A4 and NY-ESO-1 cancer-testis antigens and T cell infiltration in non-small cell lung carcinoma and their prognostic significance.

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5.  Cancer-testis antigens: expression and correlation with survival in human urothelial carcinoma.

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Journal:  Clin Cancer Res       Date:  2006-09-15       Impact factor: 12.531

6.  Immunohistochemical and molecular analysis of human melanomas for expression of the human cancer-testis antigens NY-ESO-1 and LAGE-1.

Authors:  Hilary A Vaughan; Suzanne Svobodova; Duncan Macgregor; Sue Sturrock; Achim A Jungbluth; Judy Browning; Ian D Davis; Philip Parente; Yao-Tseng Chen; Elisabeth Stockert; Fiona St Clair; Lloyd J Old; Jonathan Cebon
Journal:  Clin Cancer Res       Date:  2004-12-15       Impact factor: 12.531

7.  Expression profile of cancer-testis genes in transitional cell carcinoma of the bladder.

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Journal:  Urol Oncol       Date:  2011-03-10       Impact factor: 3.498

Review 8.  The continuum of cancer immunosurveillance: prognostic, predictive, and mechanistic signatures.

Authors:  Jérôme Galon; Helen K Angell; Davide Bedognetti; Francesco M Marincola
Journal:  Immunity       Date:  2013-07-25       Impact factor: 31.745

9.  Expression of MAGE-A3, NY-ESO-1, LAGE-1 and PRAME in urothelial carcinoma.

Authors:  L Dyrskjøt; K Zieger; T Kissow Lildal; T Reinert; O Gruselle; T Coche; M Borre; T F Ørntoft
Journal:  Br J Cancer       Date:  2012-05-17       Impact factor: 7.640

10.  PRAME is a golgi-targeted protein that associates with the Elongin BC complex and is upregulated by interferon-gamma and bacterial PAMPs.

Authors:  Frances R Wadelin; Joel Fulton; Hilary M Collins; Nikolaos Tertipis; Andrew Bottley; Keith A Spriggs; Franco H Falcone; David M Heery
Journal:  PLoS One       Date:  2013-02-27       Impact factor: 3.240

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  4 in total

1.  Opa interacting protein 5 acts as an oncogene in bladder cancer.

Authors:  Xuefeng He; Jianquan Hou; Jigen Ping; Duangai Wen; Jun He
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2.  Comprehensive Analysis to Identify MAGEA3 Expression Correlated With Immune Infiltrates and Lymph Node Metastasis in Gastric Cancer.

Authors:  Jinji Jin; Jianxin Tu; Jiahuan Ren; Yiqi Cai; Wenjing Chen; Lifang Zhang; Qiyu Zhang; Guanbao Zhu
Journal:  Front Oncol       Date:  2021-12-14       Impact factor: 6.244

3.  A Novel Multiepitope Vaccine Against Bladder Cancer Based on CTL and HTL Epitopes for Induction of Strong Immune Using Immunoinformatics Approaches.

Authors:  Ehsan Jahangirian; Ghadir A Jamal; MohammadReza Nouroozi; Alemeh Mohammadpour
Journal:  Int J Pept Res Ther       Date:  2022-02-24       Impact factor: 2.191

4.  PRAME promotes epithelial-to-mesenchymal transition in triple negative breast cancer.

Authors:  Ghaneya Al-Khadairi; Adviti Naik; Remy Thomas; Boshra Al-Sulaiti; Shaheen Rizly; Julie Decock
Journal:  J Transl Med       Date:  2019-01-03       Impact factor: 5.531

  4 in total

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