Tumor detection and elimination by a targeted gallium corrole

  1. Hasmik Agadjaniana,
  2. Jun Maa,
  3. Altan Rentsendorja,
  4. Vinod Valluripallia,
  5. Jae Youn Hwangb,
  6. Atif Mahammedc,
  7. Daniel L. Farkasb,1,
  8. Harry B. Grayd,1,
  9. Zeev Grossc,1 and
  10. Lali K. Medina-Kauwea,e,1
  1. aDepartment of Biomedical Sciences and
  2. bMinimally Invasive Surgical Technologies Institute and Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA 90048;
  3. dBeckman Institute, California Institute of Technology, Pasadena, CA 91125;
  4. cSchulich Faculty of Chemistry, Technion-Israel Institute of Technology, Haifa 32000, Israel; and
  5. eGeffen School of Medicine, University of California, Los Angeles, CA 90095
  1. Contributed by Harry B. Gray, February 15, 2009 (received for review December 18, 2008)

Abstract

Sulfonated gallium(III) corroles are intensely fluorescent macrocyclic compounds that spontaneously assemble with carrier proteins to undergo cell entry. We report in vivo imaging and therapeutic efficacy of a tumor-targeted corrole noncovalently assembled with a heregulin-modified protein directed at the human epidermal growth factor receptor (HER). Systemic delivery of this protein-corrole complex results in tumor accumulation, which can be visualized in vivo owing to intensely red corrole fluorescence. Targeted delivery in vivo leads to tumor cell death while normal tissue is spared. These findings contrast with the effects of doxorubicin, which can elicit cardiac damage during therapy and required direct intratumoral injection to yield similar levels of tumor shrinkage compared with the systemically delivered corrole. The targeted complex ablated tumors at >5 times a lower dose than untargeted systemic doxorubicin, and the corrole did not damage heart tissue. Complexes remained intact in serum and the carrier protein elicited no detectable immunogenicity. The sulfonated gallium(III) corrole functions both for tumor detection and intervention with safety and targeting advantages over standard chemotherapeutic agents.

Keywords:

Footnotes

  • 1To whom correspondence may be addressed. E-mail: hbgray{at}caltech.edu, daniel.farkas{at}cshs.org, chr10zg{at}tx.technion.ac.il, or lali.medinakauwe{at}cshs.org
  • Author contributions: H.A., D.L.F., H.B.G, Z.G., and L.K.M.-K. designed research; H.A., J.M., A.R., V.V., J.Y.H., and A.M. performed research; A.M., D.L.F., H.B.G., Z.G., and L.K.M.-K. contributed new reagents/analytic tools; H.A., D.L.F., Z.G., and L.K.M.-K. analyzed data; and D.L.F., H.B.G., Z.G., and L.K.M.-K. wrote the paper.

  • The authors declare no conflict of interest.

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0901531106/DCSupplemental.

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