Nano Research

, Volume 9, Issue 5, pp 1393–1408 | Cite as

NGR-tagged nano-gold: A new CD13-selective carrier for cytokine delivery to tumors

Open Access
Research Article

Abstract

Colloidal gold (Au), a well-tolerated nanomaterial, is currently exploited for several applications in nanomedicine. We show that gold nanoparticles tagged with a novel tumor-homing peptide containing Asn-Gly-Arg (NGR), a ligand of CD13 expressed by the tumor neovasculature, can be exploited as carriers for cytokine delivery to tumors. Biochemical and functional studies showed that the NGR molecular scaffold/linker used for gold functionalization is critical for CD13 recognition. Using fibrosarcoma-bearing mice, NGR-tagged nanodrugs could deliver extremely low, yet pharmacologically active doses of tumor necrosis factor (TNF), an anticancer cytokine, to tumors with no evidence of toxicity. Mechanistic studies confirmed that CD13 targeting was a primary mechanism of drug delivery and excluded a major role of integrin targeting consequent to NGR deamidation, a degradation reaction that generates the isoAsp-Gly-Arg (isoDGR) integrin ligand. NGR-tagged gold nanoparticles can be used, in principle, as a novel platform for single- or multi-cytokine delivery to tumor endothelial cells for cancer therapy.

Keywords

Asn-Gly-Arg (NGR) isoAsp-Gly-Arg (isoDGR) CD13 integrin tumor necrosis factor albumin gold nanoparticles 

Supplementary material

12274_2016_1035_MOESM1_ESM.pdf (2 mb)
Supplementary material, approximately 2.01 MB.

References

  1. [1]
    Curnis, F.; Sacchi, A.; Corti, A. Improving chemotherapeutic drug penetration in tumors by vascular targeting and barrier alteration. J. Clin. Invest. 2002, 110, 475–482.CrossRefGoogle Scholar
  2. [2]
    Curnis, F.; Sacchi, A.; Borgna, L.; Magni, F.; Gasparri, A.; Corti, A. Enhancement of tumor necrosis factor a antitumor immunotherapeutic properties by targeted delivery to aminopeptidase N (CD13). Nat. Biotechnol. 2000, 18, 1185–1190.CrossRefGoogle Scholar
  3. [3]
    Curnis, F.; Gasparri, A.; Sacchi, A.; Cattaneo, A.; Magni, F.; Corti, A. Targeted delivery of IFN? to tumor vessels uncouples antitumor from counterregulatory mechanisms. Cancer Res. 2005, 65, 2906–2913.CrossRefGoogle Scholar
  4. [4]
    Curnis, F.; Gasparri, A.; Sacchi, A.; Longhi, R.; Corti, A. Coupling tumor necrosis factor-a with aV integrin ligands improves its antineoplastic activity. Cancer Res. 2004, 64, 565–571.CrossRefGoogle Scholar
  5. [5]
    Gregorc, V.; Zucali, P. A.; Santoro, A.; Ceresoli, G. L.; Citterio, G.; De Pas, T. M.; Zilembo, N.; De Vincenzo, F.; Simonelli, M.; Rossoni, G. et al. Phase IIstudy of asparagineglycine- arginine-human tumor necrosis factor a, a selective vascular targeting agent, in previously treated patients with malignant pleural mesothelioma. J. Clin. Oncol. 2010, 28, 2604–2611.Google Scholar
  6. [6]
    Gregorc, V.; Citterio, G.; Vitali, G.; Spreafico, A.; Scifo, P.; Borri, A.; Donadoni, G.; Rossoni, G.; Corti, A.; Caligaris-Cappio, F. et al. Defining the optimal biological dose of NGR-hTNF, a selective vascular targeting agent, in advanced solid tumours. Eur. J. Cancer 2010, 46, 198–206.CrossRefGoogle Scholar
  7. [7]
    Corti, A.; Curnis, F.; Rossoni, G.; Marcucci, F.; Gregorc, V. Peptide-mediated targeting of cytokines to tumor vasculature: The NGR-hTNF example. BioDrugs 2013, 27, 591–603.CrossRefGoogle Scholar
  8. [8]
    Giljohann, D. A.; Seferos, D. S.; Daniel, W. L.; Massich, M. D.; Patel, P. C.; Mirkin, C. A. Gold nanoparticles for biology and medicine. Angew. Chem., Int. Ed. 2010, 49, 3280–3294.CrossRefGoogle Scholar
  9. [9]
    Cai, W. B.; Gao, T.; Hong, H.; Sun, J. T. Applications of gold nanoparticles in cancer nanotechnology. Nanotechnol. Sci. Appl. 2008, 1, 17–32.Google Scholar
  10. [10]
    Paciotti, G. F.; Myer, L.; Weinreich, D.; Goia, D.; Pavel, N.; McLaughlin, R. E.; Tamarkin, L. Colloidal gold: A novel nanoparticle vector for tumor directed drug delivery. Drug Deliv. 2004, 11, 169–183.CrossRefGoogle Scholar
  11. [11]
    Libutti, S. K.; Paciotti, G. F.; Byrnes, A. A.; Alexander, H. R.; Gannon, W. E.; Walker, M.; Seidel, G. D.; Yuldasheva, N.; Tamarkin, L. Phase I and pharmacokinetic studies of CYT-6091, a novel PEGylated colloidal gold-rhTNF nanomedicine. Clin. Cancer Res. 2010, 16, 6139–6149.CrossRefGoogle Scholar
  12. [12]
    Powell, A. C.; Paciotti, G. F.; Libutti, S. K. Colloidal gold: A novel nanoparticle for targeted cancer therapeutics. Methods Mol. Biol. 2010, 624, 375–384.CrossRefGoogle Scholar
  13. [13]
    Meng, J.; Yan, Z.; Wu, J.; Li, L.; Xue, X.; Li, M.; Li, W.; Hao, Q.; Wan, Y.; Qin, X. et al. High-yield expression, purification and characterization of tumor-targeted IFN-a2a. Cytotherapy 2007, 9, 60–68.CrossRefGoogle Scholar
  14. [14]
    Pasqualini, R.; Koivunen, E.; Kain, R.; Lahdenranta, J.; Sakamoto, M.; Stryhn, A.; Ashmun, R. A.; Shapiro, L. H.; Arap, W.; Ruoslahti, E. Aminopeptidase N is a receptor for tumor-homing peptides and a target for inhibiting angiogenesis. Cancer Res. 2000, 60, 722–727.Google Scholar
  15. [15]
    Curnis, F.; Arrigoni, G.; Sacchi, A.; Fischetti, L.; Arap, W.; Pasqualini, R.; Corti, A. Differential binding of drugs containing the NGR motif to CD13 isoforms in tumor vessels, epithelia, and myeloid cells. Cancer Res. 2002, 62, 867–874.Google Scholar
  16. [16]
    Di Matteo, P.; Arrigoni, G. L.; Alberici, L.; Corti, A.; Gallo-Stampino, C.; Traversari, C.; Doglioni, C.; Rizzardi, G. P. Enhanced expression of CD13 in vessels of inflammatory and neoplastic tissues. J. Histochem. Cytochem. 2011, 59, 47–59.CrossRefGoogle Scholar
  17. [17]
    Curnis, F.; Longhi, R.; Crippa, L.; Cattaneo, A.; Dondossola, E.; Bachi, A.; Corti, A. Spontaneous formation of L-isoaspartate and gain of function in fibronectin. J. Biol. Chem. 2006, 281, 36466–36476.CrossRefGoogle Scholar
  18. [18]
    Curnis, F.; Cattaneo, A.; Longhi, R.; Sacchi, A.; Gasparri, A. M.; Pastorino, F.; Di Matteo, P.; Traversari, C.; Bachi, A.; Ponzoni, M. et al. Critical role of flanking residues in NGRto- isoDGR transition and CD13/integrin receptor switching. J. Biol. Chem. 2010, 285, 9114–9123.CrossRefGoogle Scholar
  19. [19]
    Curnis, F.; Sacchi, A.; Gasparri, A.; Longhi, R.; Bachi, A.; Doglioni, C.; Bordignon, C.; Traversari, C.; Rizzardi, G. P.; Corti, A. Isoaspartate-glycine-arginine: A new tumor vasculature-targeting motif. Cancer Res. 2008, 68, 7073–7082.CrossRefGoogle Scholar
  20. [20]
    Corti, A.; Curnis, F. Isoaspartate-dependent molecular switches for integrin-ligand recognition. J. Cell Sci. 2011, 124, 515–522.CrossRefGoogle Scholar
  21. [21]
    Spitaleri, A.; Mari, S.; Curnis, F.; Traversari, C.; Longhi, R.; Bordignon, C.; Corti, A.; Rizzardi, G. P.; Musco, G. Structural basis for the interaction of isoDGR with the RGD-binding site of avß3 integrin. J. Biol. Chem. 2008, 283, 19757–19768.CrossRefGoogle Scholar
  22. [22]
    Frank, A. O.; Otto, E.; Mas-Moruno, C.; Schiller, H. B.; Marinelli, L.; Cosconati, S.; Bochen, A.; Vossmeyer, D.; Zahn, G.; Stragies, R. et al. Conformational control of integrinsubtype selectivity in isoDGR peptide motifs: A biological switch. Angew. Chem., Int. Ed. 2010, 49, 9278–9281.CrossRefGoogle Scholar
  23. [23]
    Bochen, A.; Marelli, U. K.; Otto, E.; Pallarola, D.; Mas-Moruno, C.; Di Leva, F. S.; Boehm, H.; Spatz, J. P.; Novellino, E.; Keßsler, H. et al. Biselectivity of isoDGR peptides for fibronectin binding integrin subtypes a5ß1 and avß6: Conformational control through flanking amino acids. J. Med. Chem. 2013, 56, 1509–1519.CrossRefGoogle Scholar
  24. [24]
    Curnis, F.; Sacchi, A.; Longhi, R.; Colombo, B.; Gasparri, A.; Corti, A. IsoDGR-tagged albumin: A new avß3 selective carrier for nanodrug delivery to tumors. Small 2013, 9, 673–678.CrossRefGoogle Scholar
  25. [25]
    Curnis, F.; Corti, A. Production and characterization of recombinant human and murine TNF. Methods Mol. Med. 2004, 98, 9–22.Google Scholar
  26. [26]
    Dondossola, E.; Rangel, R.; Guzman-Rojas, L.; Barbu, E. M.; Hosoya, H.; St John, L. S.; Molldrem, J. J.; Corti, A.; Sidman, R. L.; Arap, W. et al. CD13-positive bone marrowderived myeloid cells promote angiogenesis, tumor growth, and metastasis. Proc. Natl. Acad. Sci. USA 2013, 110, 20717–20722.CrossRefGoogle Scholar
  27. [27]
    Wong, A. H. M.; Zhou, D. X.; Rini, J. M. The X-ray crystal structure of human aminopeptidase N reveals a novel dimer and the basis for peptide processing. J. Biol. Chem. 2012, 287, 36804–36813.CrossRefGoogle Scholar
  28. [28]
    Merlot, A. M.; Kalinowski, D. S.; Richardson, D. R. Unraveling the mysteries of serum albumin-more than just a serum protein. Front. Physiol. 2014, 5, 299.CrossRefGoogle Scholar
  29. [29]
    Colombo, G.; Curnis, F.; De Mori, G. M. S.; Gasparri, A.; Longoni, C.; Sacchi, A.; Longhi, R.; Corti, A. Structureactivity relationships of linear and cyclic peptides containing the NGR tumor-homing motif. J. Biol. Chem. 2002, 277, 47891–47897.CrossRefGoogle Scholar
  30. [30]
    Liu, C.; Yang, Y.; Chen, L.; Lin, Y. L.; Li, F. A unified mechanism for aminopeptidase N-based tumor cell motility and tumor-homing therapy. J. Biol. Chem. 2014, 289, 34520–34529.CrossRefGoogle Scholar
  31. [31]
    Fields, G. B.; Noble, R. L. Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids. Int. J. Pept. Protein Res. 1990, 35, 161–214.CrossRefGoogle Scholar

Copyright information

© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2016

Authors and Affiliations

  • Flavio Curnis
    • 1
  • Martina Fiocchi
    • 1
  • Angelina Sacchi
    • 1
  • Alessandro Gori
    • 2
  • Anna Gasparri
    • 1
  • Angelo Corti
    • 1
    • 3
  1. 1.Division of Experimental OncologyIRCCS San Raffaele Scientific InstituteMilanItaly
  2. 2.Istituto di Chimica del Riconoscimento MolecolareCNRMilanItaly
  3. 3.Vita Salute San Raffaele UniversityMilanItaly

Personalised recommendations