Theranostic RGD-camptothecin conjugates, possessing a disulfide linker and a fluorescent naphthalimide moiety, were synthesized and biologically evaluated. The conjugates showed nanomolar affinity for the purified ?V?3-integrin receptor. For antiproliferative assays, the U87 human glioblastoma were chosen as ?V?3-expressing cells, whereas a non ?V?3-expressing clone (U87 ?3-KO) was generated as negative control. Although the U87 ?3-KO cells treated with the conjugates showed a statistically significant reduced fluorescence intensity (in the range 7-12 %) compared to the parental U87, internalization of the conjugates was clearly observed in both cell lines. Stability studies showed premature cleavage of the disulfide linker in the cell media, with consequent release of free camptothecin. Consistent with the results of the internalization and stability studies, the conjugates did not show significant selectivity against the U87 cells compared to the U87 ?3-KO clone.
Targeting Integrin ?V?3 with Theranostic RGD-Camptothecin Conjugates Bearing a Disulfide Linker: Biological Evaluation Reveals a Complex Scenario
Arosio D;
2017
Abstract
Theranostic RGD-camptothecin conjugates, possessing a disulfide linker and a fluorescent naphthalimide moiety, were synthesized and biologically evaluated. The conjugates showed nanomolar affinity for the purified ?V?3-integrin receptor. For antiproliferative assays, the U87 human glioblastoma were chosen as ?V?3-expressing cells, whereas a non ?V?3-expressing clone (U87 ?3-KO) was generated as negative control. Although the U87 ?3-KO cells treated with the conjugates showed a statistically significant reduced fluorescence intensity (in the range 7-12 %) compared to the parental U87, internalization of the conjugates was clearly observed in both cell lines. Stability studies showed premature cleavage of the disulfide linker in the cell media, with consequent release of free camptothecin. Consistent with the results of the internalization and stability studies, the conjugates did not show significant selectivity against the U87 cells compared to the U87 ?3-KO clone.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
