Literature DB >> 3258589

Glycoprotein P3.58, associated with tumor progression in malignant melanoma, is a novel leukocyte activation antigen.

B Holzmann1, J M Lehmann, H W Ziegler-Heitbrock, I Funke, G Riethmüller, J P Johnson.   

Abstract

The P3.58 antigen is defined by monoclonal antibodies (MAbs) selected to discriminate between benign and malignant melanocytic cells. Its expression in malignant cells has been shown to correlate with an increased risk of metastasis. A survey of a wide range of tissues revealed that, on normal tissue, expression of P3.58 antigen is restricted to a subset of cells involved in the immune response. The antigen was found not only on certain endothelia, but also on activated macrophages in vivo and in vitro and as well as on activated B lymphocytes. A comparison with known B-lymphocyte and leukocyte activation antigens indicated that P3.58 is a novel leukocyte activation antigen. Biochemical analysis of the P3.58 antigen isolated from cells of different histogenic origin indicated that different molecular forms of the antigen exist, apparently depending on the cell type of origin. P3.58 molecules precipitated from tunicamycin-treated cells were identical in all cell types, suggesting that the variation observed is due to variable N-glycosylation.

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Year:  1988        PMID: 3258589     DOI: 10.1002/ijc.2910410412

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  5 in total

1.  Individual epitopes of an 85,000 MW membrane adherence molecule are variably expressed on cells of different lineage.

Authors:  T F Schulz; W Vogetseder; M Mitterer; G Böck; J P Johnson; M P Dierich
Journal:  Immunology       Date:  1988-08       Impact factor: 7.397

Review 2.  Cell adhesion receptor expression during melanoma progression and metastasis.

Authors:  I R Hart; M Birch; J F Marshall
Journal:  Cancer Metastasis Rev       Date:  1991-06       Impact factor: 9.264

3.  De novo expression of intercellular-adhesion molecule 1 in melanoma correlates with increased risk of metastasis.

Authors:  J P Johnson; B G Stade; B Holzmann; W Schwäble; G Riethmüller
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

4.  Critical role of reactive oxygen species (ROS) for synergistic enhancement of apoptosis by vemurafenib and the potassium channel inhibitor TRAM-34 in melanoma cells.

Authors:  Daniel Bauer; Felix Werth; Ha An Nguyen; Felix Kiecker; Jürgen Eberle
Journal:  Cell Death Dis       Date:  2017-02-02       Impact factor: 8.469

5.  HLA class I downregulation is associated with enhanced NK-cell killing of melanoma cells with acquired drug resistance to BRAF inhibitors.

Authors:  Rosa Sottile; Pradeepa N Pangigadde; Thomas Tan; Andrea Anichini; Francesco Sabbatino; Francesca Trecroci; Elvira Favoino; Laura Orgiano; James Roberts; Soldano Ferrone; Klas Kärre; Francesco Colucci; Ennio Carbone
Journal:  Eur J Immunol       Date:  2015-12-20       Impact factor: 5.532

  5 in total

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