Somatostatin Analogues for Receptor Targeted Photodynamic Therapy

Slavka Kascakova, Leo Hofland, Riëtte de Bruijn, YP Ye, S Achilefu, K (Katy) van der Wansem, A van den Heuvel, Peter van Koetsveld, Michel Brugts, Aart Jan Lelij, Dick Sterenborg, Timo ten Hagen, Dominic Robinson, P.M. van Hagen

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Abstract

Photodynamic therapy (PDT) is an established treatment modality, used mainly for anticancer therapy that relies on the interaction of photosensitizer, light and oxygen. For the treatment of pathologies in certain anatomical sites, improved targeting of the photosensitizer is necessary to prevent damage to healthy tissue. We report on a novel dual approach of targeted PDT (vascular and cellular targeting) utilizing the expression of neuropeptide somatostatin receptor (sst(2)) on tumor and neovascular-endothelial cells. We synthesized two conjugates containing the somatostatin analogue [Tyr3]-octreotate and Chlorin e6 (Ce6): Ce6-K-3-[Tyr3]-octreotate (1) and Ce6-[Tyr3]-octreotate-K-3-[Tyr3]-octreotate (2). Investigation of the uptake and photodynamic activity of conjugates in-vitro in human erythroleukemic K562 cells showed that conjugation of [Tyr3]-octreotate with Ce6 in conjugate 1 enhances uptake (by a factor 2) in cells over-expressing sst(2) compared to wildtype cells. Co-treatment with excess free Octreotide abrogated the phototoxicity of conjugate 1 indicative of a specific sst(2)-mediated effect. In contrast conjugate 2 showed no receptor-mediated effect due to its high hydrophobicity. When compared with un-conjugated Ce6, the PDT activity of conjugate 1 was lower. However, it showed higher photostability which may compensate for its lower phototoxicity. Intra-vital fluorescence pharmacokinetic studies of conjugate 1 in rat skin-fold observation chambers transplanted with sst(2)(+) AR42J acinar pancreas tumors showed significantly different uptake profiles compared to free Ce6. Co-treatment with free Octreotide significantly reduced conjugate uptake in tumor tissue (by a factor 4) as well as in the chamber neo-vasculature. These results show that conjugate 1 might have potential as an in-vivo sst(2) targeting photosensitizer conjugate.
Original languageUndefined/Unknown
JournalPLoS One (print)
Volume9
Issue number8
DOIs
Publication statusPublished - 2014

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