• Title of article

    RAP80/UIMC1 as cancer-associated antigen: Alternative splice variants and their immunogenicity

  • Author/Authors

    Shebzukhov، نويسنده , , Yuriy V. and Koroleva، نويسنده , , Ekaterina P. and Khlgatian، نويسنده , , Svetlana V. and Belousov، نويسنده , , Pavel V. and Sazykin، نويسنده , , Alexey Y. and Kadachigova، نويسنده , , Tatiana S. and Pomerantseva، نويسنده , , Ekaterina A. and Lagarkova، نويسنده , , Maria A. and Nedospasov، نويسنده , , Sergei A. and Kuprash، نويسنده , , Dmitry V.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2007
  • Pages
    8
  • From page
    255
  • To page
    262
  • Abstract
    We have identified RAP80/UIMC1, the protein highly expressed in testis, as a new cancer-associated antigen. Sera from 5% to 10% of patients with different types of cancer contain specific antibodies to RAP80/UIMC1. In order to investigate the possible reasons for RAP80/UIMC1 immunogenicity, we characterized its numerous splice isoforms and mapped immunogenic regions of the protein. The majority of RAP80/UIMC1 transcripts was detected both in normal tissues and in colon tumors. There are several RAP80/UIMC1 isoforms that are predominantly expressed in testis, however we did not observe elevated expression of these transcripts in tumors from seropositive patients. We mapped the major immunogenic region of RAP80/UIMC1 to the central part of the protein encoded by exon 9 which is present in a number of ubiquitous splice forms. Thus, based on our data, autoreactivity to RAP80/UIMC1 is related to reasons other than overexpression or tumor-specific splicing.
  • Keywords
    SEREX , Transcription , Colon cancer
  • Journal title
    Cancer Letters
  • Serial Year
    2007
  • Journal title
    Cancer Letters
  • Record number

    1810760