Literature DB >> 12587428

[The role of membrane glycoproteins CD46, CD55 and CD59 in protection of tumor cells against complement lysis].

Dorota Wojnicz1, Julia Bar, Stanisław Jankowski.   

Abstract

Utilization of the complement system offers potential for the elimination of tumor cells by monoclonal antibodies (mAb) immunotherapy. Activation of the complement system causes tumor cell destruction by inducing complement lysis and promoting cell-mediated killing. In addition, complement can induce a strong inflammatory response, which might enhance other antitumor effector mechanisms. An important targets for mAb immunotherapy, however, are membrane bound complement regulatory glycoprotein: CD46, CD55 and CD59, which have been found to be expressed on most tumor cells in vivo and in vitro. Blocking or down regulation of these inhibitors could be an important step in the advancement of mAb immunotherapy.

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Year:  2002        PMID: 12587428

Source DB:  PubMed          Journal:  Postepy Hig Med Dosw        ISSN: 0032-5449            Impact factor:   0.270


  3 in total

1.  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

2.  Possible role of complement factors and their inhibitors in the myocardial infarction: an immunohistochemical study.

Authors:  Tomasz Ilczuk; Aleksander Wasiutynski; Ewa Wilczek; Barbara Gornicka
Journal:  Cent Eur J Immunol       Date:  2014-06-27       Impact factor: 2.085

3.  Characterization of CD46 and β1 integrin dynamics during sperm acrosome reaction.

Authors:  Michaela Frolikova; Natasa Sebkova; Lukas Ded; Katerina Dvorakova-Hortova
Journal:  Sci Rep       Date:  2016-09-26       Impact factor: 4.379

  3 in total

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