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Molecular Cancer Therapeutics
Molecular Cancer Therapeutics
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Research Article

An infrared dye-conjugated virus-like particle for the treatment of primary uveal melanoma

Rhonda C Kines, Isabella Varsavsky, Sanghamitra Choudhary, Debaditya Bhattacharya, Sean Spring, Roger J. McLaughlin, Shin J Kang, Hans E Grossniklaus, Demitrios G Vavvas, Stephen Monks, John R MacDougall, Elisabet de los Pinos and John T Schiller
Rhonda C Kines
1Research, Aura Biosciences
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  • For correspondence: rkines@aurabiosciences.com
Isabella Varsavsky
1Research, Aura Biosciences
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Sanghamitra Choudhary
1Research, Aura Biosciences
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Debaditya Bhattacharya
1Research, Aura Biosciences
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Sean Spring
1Research, Aura Biosciences
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Roger J. McLaughlin
1Research, Aura Biosciences
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Shin J Kang
2Opthalmology, Emory University
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Hans E Grossniklaus
3Ophthalmology, Emory Univ.
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Demitrios G Vavvas
4Angiogenesis Laboratory Retina Service, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School
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Stephen Monks
1Research, Aura Biosciences
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John R MacDougall
1Research, Aura Biosciences
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Elisabet de los Pinos
1Research, Aura Biosciences
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John T Schiller
5CCR, National Cancer Institute
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DOI: 10.1158/1535-7163.MCT-17-0953
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Abstract

The work outlined herein describes AU-011, a novel recombinant papillomavirus-like particle (VLP) drug conjugate and its initial evaluation as a potential treatment for primary uveal melanoma. The VLP is conjugated with a phthalocyanine photosensitizer, IRDye 700DX, that exerts its cytotoxic effect through photo-activation with a near-infrared laser. We assessed the anti-cancer properties of AU-011 in vitro utilizing a panel of human cancer cell lines and in vivo using murine subcutaneous and rabbit orthotopic xenograft models of uveal melanoma. The specificity of VLP binding (tumor targeting), mediated through cell surface heparan sulfate proteoglycans (HSPG), was assessed using HSPG deficient cells and by inclusion of heparin in in vitro studies. Our results provide evidence of potent and selective anti-cancer activity, both in vitro and in vivo. AU-011 activity was blocked by inhibiting its association with HSPG using heparin and using cells lacking surface HSPG, indicating that the tumor tropism of the VLP was not affected by dye conjugation and cell association is critical for AU-011 mediated cytotoxicity. Using the uveal melanoma xenograft models, we observed tumor uptake following intravenous (murine) and intravitreal (rabbit) administration and, after photoactivation, potent dose-dependent tumor responses. Further, in the rabbit orthotopic model, which closely models uveal melanoma as it presents in the clinic, tumor treatment spared the retina and adjacent ocular structures. Our results support further clinical development of this novel therapeutic modality that might transform visual outcomes and provide a targeted therapy for the early stage treatment of patients with this rare and life-threatening disease.

  • Received September 27, 2017.
  • Revision received December 1, 2017.
  • Accepted December 8, 2017.
  • Copyright ©2017, American Association for Cancer Research.
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This OnlineFirst version was published on December 14, 2017
doi: 10.1158/1535-7163.MCT-17-0953

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An infrared dye-conjugated virus-like particle for the treatment of primary uveal melanoma
Rhonda C Kines, Isabella Varsavsky, Sanghamitra Choudhary, Debaditya Bhattacharya, Sean Spring, Roger J. McLaughlin, Shin J Kang, Hans E Grossniklaus, Demitrios G Vavvas, Stephen Monks, John R MacDougall, Elisabet de los Pinos and John T Schiller
Mol Cancer Ther December 14 2017 DOI: 10.1158/1535-7163.MCT-17-0953

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An infrared dye-conjugated virus-like particle for the treatment of primary uveal melanoma
Rhonda C Kines, Isabella Varsavsky, Sanghamitra Choudhary, Debaditya Bhattacharya, Sean Spring, Roger J. McLaughlin, Shin J Kang, Hans E Grossniklaus, Demitrios G Vavvas, Stephen Monks, John R MacDougall, Elisabet de los Pinos and John T Schiller
Mol Cancer Ther December 14 2017 DOI: 10.1158/1535-7163.MCT-17-0953
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Molecular Cancer Therapeutics
eISSN: 1538-8514
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