Vascular ligand-receptor mapping by direct combinatorial selection in cancer patients

  • Fernanda I Staquicini
  • Marina Cardó-Vila
  • Mikhail G Kolonin
  • Martin Trepel
  • Julianna K Edwards
  • Diana N Nunes
  • Anna Sergeeva
  • Eleni Efstathiou
  • Jessica Sun
  • Nalvo F Almeida
  • Shi-Ming Tu
  • Gregory H Botz
  • Michael J Wallace
  • David J O'Connell
  • Stan Krajewski
  • Jeffrey E Gershenwald
  • Jeffrey J Molldrem
  • Anne L Flamm
  • Erkki Koivunen
  • Rebecca D Pentz
  • Emmanuel Dias-Neto
  • João C Setubal
  • Dolores J Cahill
  • Patricia Troncoso
  • Kim-Ahn Do
  • Christopher J Logothetis
  • Richard L Sidman
  • Renata Pasqualini
  • Wadih Arap

Abstract

Molecules differentially expressed in blood vessels among organs or between damaged and normal tissues, are attractive therapy targets; however, their identification within the human vasculature is challenging. Here we screened a peptide library in cancer patients to uncover ligand-receptors common or specific to certain vascular beds. Surveying ~2.35 x 10(6) motifs recovered from biopsies yielded a nonrandom distribution, indicating that systemic tissue targeting is feasible. High-throughput analysis by similarity search, protein arrays, and affinity chromatography revealed four native ligand-receptors, three of which were previously unrecognized. Two are shared among multiple tissues (integrin α4/annexin A4 and cathepsin B/apolipoprotein E3) and the other two have a restricted and specific distribution in normal tissue (prohibitin/annexin A2 in white adipose tissue) or cancer (RAGE/leukocyte proteinase-3 in bone metastases). These findings provide vascular molecular markers for biotechnology and medical applications.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0027-8424
DOIs
StatusVeröffentlicht - 15.11.2011
Extern publiziertJa
PubMed 22049339