Literature DB >> 17492842

An update on malignant melanoma vaccine research: insights into mechanisms for improving the design and potency of melanoma therapeutic vaccines.

Stephen John Ralph1.   

Abstract

Currently, cancer vaccine therapy for melanoma has a 2-fold focus. On the one hand, advances have been aimed at improving the effectiveness of melanoma vaccines based on a greater understanding of melanoma tumor cell biology. On the other hand, there is increasing evidence that the immune system, our defense against tumors, also inadvertently plays a supportive role in promoting the development and progression of tumors. Hence, two opposing forces 'hanging in the balance' dictate patients' responses to melanoma: tumor cell biology and the status of the immune system. Recent developments in our understanding of both of these aspects have provided new leads and insights for novel ways to improve vaccine design and add to the melanoma vaccine armory. As the focus of immunotherapy shifts its aim towards the tumor microenvironment, we are now developing the ability to program the immune responses raised by vaccination against melanoma. The aim here is to prevent myeloid and regulatory T-cell-mediated immune suppression as well as to counteract tumor-derived factors capable of suppressing immune responses. A redirected strategy for vaccine immunotherapy is proposed based on our greater understanding of tumor immunity. Using a combination therapy of immune-potentiating melanoma vaccines together with adjuvants for overcoming the immunosuppressive forces will allow us to activate protective immunity against melanoma. Other cancer vaccines (i.e. colon or renal) are already offering reasons for hope and expectation that vaccine immunotherapy will also produce successful outcomes for patients with melanoma.

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Year:  2007        PMID: 17492842     DOI: 10.2165/00128071-200708030-00001

Source DB:  PubMed          Journal:  Am J Clin Dermatol        ISSN: 1175-0561            Impact factor:   7.403


  10 in total

1.  In vivo 6-thioguanine-resistant T cells from melanoma patients have public TCR and share TCR beta amino acid sequences with melanoma-reactive T cells.

Authors:  Cindy L Zuleger; Michael D Macklin; Bret L Bostwick; Qinglin Pei; Michael A Newton; Mark R Albertini
Journal:  J Immunol Methods       Date:  2010-12-21       Impact factor: 2.303

Review 2.  Dormancy of metastatic melanoma.

Authors:  Liliana Ossowski; Julio A Aguirre-Ghiso
Journal:  Pigment Cell Melanoma Res       Date:  2009-10-19       Impact factor: 4.693

Review 3.  Phosphoproteomics and cancer research.

Authors:  Keith Ashman; Elena López Villar
Journal:  Clin Transl Oncol       Date:  2009-06       Impact factor: 3.405

4.  Cell proliferation in cutaneous malignant melanoma: relationship with neoplastic progression.

Authors:  G E Piérard
Journal:  ISRN Dermatol       Date:  2012-01-11

5.  BAP31, a promising target for the immunotherapy of malignant melanomas.

Authors:  Shaojuan Yu; Fuli Wang; Li Fan; Yuying Wei; Haitao Li; Yuanjie Sun; Angang Yang; Boquan Jin; Chaojun Song; Kun Yang
Journal:  J Exp Clin Cancer Res       Date:  2015-04-18

6.  Phosphoproteomics Reveals HMGA1, a CK2 Substrate, as a Drug-Resistant Target in Non-Small Cell Lung Cancer.

Authors:  Yi-Ting Wang; Szu-Hua Pan; Chia-Feng Tsai; Ting-Chun Kuo; Yuan-Ling Hsu; Hsin-Yung Yen; Wai-Kok Choong; Hsin-Yi Wu; Yen-Chen Liao; Tse-Ming Hong; Ting-Yi Sung; Pan-Chyr Yang; Yu-Ju Chen
Journal:  Sci Rep       Date:  2017-03-14       Impact factor: 4.379

7.  Eukaryotic elongation factor 2 is a prognostic marker and its kinase a potential therapeutic target in HCC.

Authors:  Leona L Pott; Sascha Hagemann; Henning Reis; Kristina Lorenz; Thilo Bracht; Thomas Herold; Boris V Skryabin; Dominik A Megger; Julia Kälsch; Frank Weber; Barbara Sitek; Hideo A Baba
Journal:  Oncotarget       Date:  2017-02-14

Review 8.  Phosphoproteomics and lung cancer research.

Authors:  Elena López; William C S Cho
Journal:  Int J Mol Sci       Date:  2012-09-26       Impact factor: 5.923

9.  Surface antigen profiles of leukocytes and melanoma cells in lymph node metastases are associated with survival in AJCC stage III melanoma patients.

Authors:  Kimberley L Kaufman; Swetlana Mactier; Nicola J Armstrong; Duthika Mallawaaratchy; Scott N Byrne; Lauren E Haydu; Valerie Jakrot; John F Thompson; Graham J Mann; Richard A Scolyer; Richard I Christopherson
Journal:  Clin Exp Metastasis       Date:  2014-01-17       Impact factor: 5.150

10.  Apurinic/apyrimidinic endonuclease/redox effector factor-1(APE/Ref-1): a unique target for the prevention and treatment of human melanoma.

Authors:  Sun Yang; Frank L Meyskens
Journal:  Antioxid Redox Signal       Date:  2009-03       Impact factor: 8.401

  10 in total

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