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TSPO 18 kDa (PBR) targeted photosensitizers for cancer imaging (PET) and PDT

  • Roswell Park Cancer Institute
  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

Translocator protein (TSPO) 18 kDa overexpression has been observed in a large variety of human cancers, especially breast cancers. PK 11195, an isoquinoline analogue, is one of the ligands of highest TSPO binding affinity. Due to the long biological half life of our photosensitizers, there is a need to label them with a long lived radioisotope, for example I-124. Our objectives are to find translocator protein targeted photosensitizers for both tumor imaging (PET) and photodynamic therapy (PDT). I-PK 11195 is conjugated with the tumor avid photosensitizer HPPH. We find that those two tumor avid components complement each other and make the conjugate molecule even more tumor avid; compared to the photosensitizer itself, the conjugate is found to show improved PDT efficacy. It is concluded that I-PK 11195 can be a good vehicle to deliver radionuclide and photosensitizer to TSPO overexpressed tumor regions. Such conjugates could be useful for both tumor imaging (PET) and PDT.

Original languageEnglish
Pages (from-to)136-141
Number of pages6
JournalACS Medicinal Chemistry Letters
Volume2
Issue number2
DOIs
StatePublished - Feb 10 2011

Keywords

  • PK 11195
  • Photodynamic therapy (PDT)
  • cancer target specific
  • peripheral benzodiazepine receptor (PBR)
  • positron emission tomography (PET)
  • translocator protein (TSPO)

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