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Plexin D1: new potential biomarker for cervical cancer.

Abstract
To explore possible role of Plexin D1 in cancer angiogenesis with special focus on cervical cancer. Twelve various normal tissues, 12 various tumor samples, and 59 different stages of cervical cancer samples on tissue microarrays were examined for the expression of Plexin D1. The findings of our study clearly indicate that Plexin D1 is strongly associated with cellular differentiation in the tissues investigated, and that expression is strongly dependent on the tumor histotype. In some tumor subtypes, the protein was detected at several-fold higher levels than was found in the corresponding normal tissues, while in others, expression was similar to normal tissues. Most significantly, strong expression was detected in the endothelial cells of the cervical cancer samples, yet no expression was seen in endothelial cells of normal cervical tissues, which suggests a potential role of Plexin D1 in cervical cancer-associated angiogenesis.Regarding the implications of Plexin D1 and its associations with cancer angiogenesis, it might be a potential cervical cancer biomarker if further studies confirm the present preliminary findings.
AuthorsManal Aly Shalaby, Lynne Hampson, Anthony Oliver, Ian Hampson
JournalJournal of immunoassay & immunochemistry (J Immunoassay Immunochem) Vol. 33 Issue 3 Pg. 223-33 ( 2012) ISSN: 1532-4230 [Electronic] England
PMID22738647 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers, Tumor
  • Cell Adhesion Molecules, Neuronal
  • Intracellular Signaling Peptides and Proteins
  • Membrane Glycoproteins
  • PLXND1 protein, human
Topics
  • Adult
  • Aged
  • Biomarkers, Tumor (metabolism)
  • Cell Adhesion Molecules, Neuronal (metabolism)
  • Cell Differentiation
  • Endothelial Cells (metabolism)
  • Female
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Membrane Glycoproteins
  • Middle Aged
  • Neovascularization, Pathologic
  • Uterine Cervical Neoplasms (metabolism, pathology)

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