Literature DB >> 12172427

Role of prostate stem cell antigen in prostate cancer research.

Mark W Jalkut1, Robert E Reiter.   

Abstract

PURPOSE OF REVIEW: The identification of cell surface antigens is critical to the development of future prognostic and therapeutic modalities for the treatment of prostate cancer. Several prostate-specific proteins have been identified and are under investigation. This review reports on prostate stem cell antigen (PSCA), a protein with restricted expression that may have prognostic and therapeutic utility. RECENT
FINDINGS: PSCA is a glycosylphosphatidylinositol-anchored cell-surface protein belonging to the Ly-6/Thy-1 family of cell surface antigens, and a murine homologue has been described. It is expressed in the normal human prostate and overexpressed in human prostate cancers. Its overexpression has been correlated with increased Gleason score, advanced stage and bone metastasis. PSCA is co-amplified with MYC, an independent predictor of progression and death. PSCA may therefore be a useful predictor of tumor biology and a useful target of immunotherapy against prostate cancer. Evidence suggests a potential role in strategies employing cytotoxic T cell lymphocytes. Anti-tumor activity has been demonstrated with monoclonal antibodies in tumor take and established tumor xenograft models. Conjugated antibody has recently been reported to have anti-tumor activity in preclinical models.
SUMMARY: PSCA may serve as a tool in refining the prognosis of an individual cancer and may be a useful therapeutic target for immunotherapy. Future studies will be required to confirm its clinical utility as a prognostic factor. Future animal and clinical studies will be required to test various immunotherapy strategies for safety and efficacy. The study of PSCA regulation and expression may provide information on normal prostate development and prostate carcinogenesis.

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Year:  2002        PMID: 12172427     DOI: 10.1097/00042307-200209000-00006

Source DB:  PubMed          Journal:  Curr Opin Urol        ISSN: 0963-0643            Impact factor:   2.309


  7 in total

1.  Growth delay of human bladder cancer cells by Prostate Stem Cell Antigen downregulation is associated with activation of immune signaling pathways.

Authors:  Emanuele Marra; Paolo Uva; Valentina Viti; Valeria Simonelli; Eugenia Dogliotti; Emanuele De Rinaldis; Armin Lahm; Nicola La Monica; Alfredo Nicosia; Gennaro Ciliberto; Fabio Palombo
Journal:  BMC Cancer       Date:  2010-04-07       Impact factor: 4.430

2.  New gene expressed in prostate: a potential target for T cell-mediated prostate cancer immunotherapy.

Authors:  Vittore Cereda; Diane J Poole; Claudia Palena; Sudipto Das; Tapan K Bera; Cinzia Remondo; James L Gulley; Philip M Arlen; Junko Yokokawa; Ira Pastan; Jeffrey Schlom; Kwong Y Tsang
Journal:  Cancer Immunol Immunother       Date:  2009-06-04       Impact factor: 6.968

Review 3.  Prostate stem cell antigen: a prospective therapeutic and diagnostic target.

Authors:  Adam B Raff; Andrew Gray; W Martin Kast
Journal:  Cancer Lett       Date:  2008-10-05       Impact factor: 8.679

Review 4.  Antibodies targeting cancer stem cells: a new paradigm in immunotherapy?

Authors:  Mahendra P Deonarain; Christina A Kousparou; Agamemnon A Epenetos
Journal:  MAbs       Date:  2009 Jan-Feb       Impact factor: 5.857

5.  CD177: A member of the Ly-6 gene superfamily involved with neutrophil proliferation and polycythemia vera.

Authors:  David F Stroncek; Lorraine Caruccio; Maria Bettinotti
Journal:  J Transl Med       Date:  2004-03-29       Impact factor: 5.531

Review 6.  Cancer therapy using tumor-associated antigens to reduce side effects.

Authors:  David Siu
Journal:  Clin Exp Med       Date:  2009-05-01       Impact factor: 5.057

7.  Systemic treatment with CAR-engineered T cells against PSCA delays subcutaneous tumor growth and prolongs survival of mice.

Authors:  Victoria Hillerdal; Mohanraj Ramachandran; Justyna Leja; Magnus Essand
Journal:  BMC Cancer       Date:  2014-01-18       Impact factor: 4.430

  7 in total

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