Literature DB >> 12641491

Prostate cancer: advances in immunotherapy.

Arthur A Hurwitz1, Paul Yanover, Mary Markowitz, James P Allison, Eugene D Kwon.   

Abstract

The absence of curative therapies for advanced or recurrent forms of prostate cancer has prompted a vigorous search for novel treatment strategies. Immunotherapy encompasses one particularly promising systemic approach to the treatment of prostate cancer. Immune-based strategies for treating prostate cancer have recently been facilitated by the identification of a number of prostate tissue/tumour antigens that can be targeted, either by antibody or T cells, to promote prostate tumour cell injury or death. These same prostate antigens can also be used for the construction of vaccines to induce prostate-specific T cell-mediated immunity. Greater insight into specific mechanisms that govern antigen-specific T cell activation has brought with it a number of innovative methods to induce and enhance T cell-mediated responses against prostate tumours. For instance, autologous dendritic cells loaded with prostate antigens have proved useful to induce prostate-specific T cell activation. Similarly, in vivo manipulations of T cell costimulatory pathway receptors can greatly facilitate tumour-specific T cell activation and potentiate T cell-mediated responses against a number of malignancies, including prostate cancer. For example, blocking T cell cytotoxic lymphocyte-associated antigen 4 (CTLA-4) receptor binding to its ligand prevents the down-regulation of T cell responses and can even potentiate T cell antitumoural immunity in mouse models of prostate cancer. Androgen ablation (AA) may induce prostate tumour/tissue-specific T cell mediated inflammation and, as such, a phase II trial is currently in progress to ascertain whether CTLA-4 blockade can enhance AA-induced treatment responses in patients with advanced prostate cancer. Nevertheless, further basic and clinical investigation is still required to establish immunotherapy as a true prostate cancer treatment option.

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Year:  2003        PMID: 12641491     DOI: 10.2165/00063030-200317020-00005

Source DB:  PubMed          Journal:  BioDrugs        ISSN: 1173-8804            Impact factor:   5.807


  5 in total

Review 1.  Cancer immunotherapy: sipuleucel-T and beyond.

Authors:  Aimee E Hammerstrom; Diana H Cauley; Bradley J Atkinson; Padmanee Sharma
Journal:  Pharmacotherapy       Date:  2011-08       Impact factor: 4.705

2.  A national multicenter phase 2 study of prostate-specific antigen (PSA) pox virus vaccine with sequential androgen ablation therapy in patients with PSA progression: ECOG 9802.

Authors:  Robert S DiPaola; Yu-Hui Chen; Glenn J Bubley; Mark N Stein; Noah M Hahn; Michael A Carducci; Edmund C Lattime; James L Gulley; Philip M Arlen; Lisa H Butterfield; George Wilding
Journal:  Eur Urol       Date:  2014-12-18       Impact factor: 20.096

3.  Inhibition of decay-accelerating factor (CD55) attenuates prostate cancer growth and survival in vivo.

Authors:  Robert D Loberg; LaShon L Day; Rodney Dunn; Linda M Kalikin; Kenneth J Pienta
Journal:  Neoplasia       Date:  2006-01       Impact factor: 5.715

4.  Future perspectives of prostate cancer therapy.

Authors:  Murali Gururajan; Edwin M Posadas; Leland W K Chung
Journal:  Transl Androl Urol       Date:  2012-01-03

5.  From "Hellstrom Paradox" to anti-adenosinergic cancer immunotherapy.

Authors:  Dmitriy Lukashev; Michail Sitkovsky; Akio Ohta
Journal:  Purinergic Signal       Date:  2007-01-24       Impact factor: 3.765

  5 in total

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