Targeted Particle Fools Brain's Guardian to Reach Tumors
MD Anderson News Release 02/01/2011
By impersonating iron, binding agent glides through the blood-brain barrier
MD Anderson News Release 02/01/11
A targeted delivery combination selectively crosses the tight barrier that protects the brain from the bloodstream to home in on and bind to brain tumors, a research team led by scientists from The University of Texas MD Anderson Cancer Center reported in the January issue of the Journal of Clinical Investigation.
In experiments with mice, the researchers demonstrated that the targeted particles guide payloads to image tumors, treat tumors, or can potentially do both to monitor treatment as it occurs. Their findings open a new research avenue for detecting and treating brain tumors in human patients.
"We've identified an iron-mimic peptide that can hitch a ride on a protein complex that transports iron across the blood-brain barrier," said co-senior author Wadih Arap, M.D., Ph.D., professor in the David H. Koch Center at MD Anderson. "Employing the iron transport system selectively opens the blood-brain barrier for tumor imaging and treatment while keeping it otherwise intact to play its protective role."
The barrier thwarts drug delivery because its tight layering of blood vessel cells and certain types of brain cells forms a nearly impenetrable wall against most blood-borne compounds, which can harm the brain. The iron-transporting transferrin protein and receptor complex is a potential path to treatment, the authors noted, because its receptor gene is the most overexpressed in human glioblastomas.
Glioblastomas are the most common form of primary brain tumor among adults and are one of the most lethal cancers -- patients have a median survival rate of one year. They resist radiation and chemotherapy and often invade areas of the brain where full surgical removal is impossible.
Peptide + viral particle = targeting
Arap and Renata Pasqualini, Ph.D., professor in the Koch Center and co-senior author on the paper, developed the screening, targeting and delivery processes used in the project. The combination consists of a viral particle called phage packaged with a bit of protein, or peptide, which acts as a ligand, binding to the target.
"This particular delivery system can evolve on many fronts, but we think imaging will probably be the first priority," Pasqualini said. "Brain tumors invade the brain in unpredictable ways, making surgery and targeted therapy a challenge. Ligand-directed imaging based on this technology might improve existing treatment strategies."
The team is working toward phase I human clinical trials, but required preclinical steps will take at least two years. "Our priority is the rapid translation of our approach into clinical applications, an effort that will greatly benefit from the collaborative, multidisciplinary nature of this project," said co-first author Fernanda Staquicini, Ph.D., a postdoctoral fellow in the Arap-Pasqualini lab.
The researchers screened potential binding agents to brain blood vessel cells in mice from a library of small peptides attached to viral particles. Analysis narrowed 30 candidates out of hundreds screened down to one peptide: CRTIGPSVC, a portion of the transferrin protein.
The iron-binding protein tranferrin has two conformations, one when it's iron-free (open) and another when it contains iron (closed). Experiments showed that CRTIGPSVC connects with the open form, converting the protein to a state similar to the closed form, as if it were carrying iron. The closed form binds to transferrin receptors, which exist in abundance in glioblastoma.
Peptide phage selectively sticks with tumors
The CRTIGPSVC peptide phage was given to mice with human-derived malignant glioma. An hour later, the tumors harbored high levels of the peptide phage, which appeared at only background levels in normal tissue.
Immunostaining showed the peptide phage gathered in both the tumor's blood vessels and tumor tissue, indicating that it passed from the blood vessels to tumor cells.
Guided payloads shrink and image tumors
The CRTIGPSVC peptide was then connected to a viral delivery system loaded with a gene from the Herpes' simplex virus known as HSVtk. It serves as a reporter gene for molecular imaging with PET scans and causes cells to kill themselves when given with the drug ganciclovir.
- Mice treated with the CRTIGPSVC-targeted versions loaded with the HSVtk gene had tumors that were typically half the size of those in mice treated with the untargeted delivery system when both groups were treated with ganciclovir.
- Blood vessel and glioma cells forced to commit suicide (apoptosis) were found throughout the tumors of mice treated with the peptide-targeted delivery system. Cell suicide did not occur above background levels in normal brain tissue.
- PET/CT scans showed widespread targeting of tumor tissue with little or no signal in normal tissue.
The team analyzed expression of the transferrin receptor in 165 samples of human tumors. A strong or moderate presence of the receptor was found on 85 percent of glioblastoma samples, indicating that the receptor might be a suitable target for human use.
Beyond cancer: Genetic defects, neurodegenerative diseases
Peptide-guided delivery of drugs or imaging agents could apply to other diseases of the central nervous system, said co-author Richard Sidman, M.D., emeritus professor of neuropathology at Harvard Medical School and the Department of Neurology at Beth Deaconess Medical Center.
"One important set of diseases to test will be lysosomal storage diseases, mostly lethal in childhood or adolescence, in each of which a different crucial brain enzyme is markedly reduced or absent because of a defect in the corresponding gene," Sidman said. "These diseases can be treated by provision to the brain of 25 percent or less of the missing enzyme. Therefore, the prospect merits testing as to whether delivery of even modest amounts of the normal version of the pertinent gene across the blood-brain barrier would be therapeutically effective."
Prospects for radiologically diagnosing and treating strokes, traumatic injury and neurodegenerative diseases such as Alzheimer's, Parkinson's, and Huntington's diseases, also are worth pursuing, Sidman noted.
An accompanying commentary in JCI notes the flexibility and utility of the researchers' plan of attack. "We can look forward to future applications of this approach for the discovery of new druggable targets and the identification of cell surface molecules that may be important in many types of cancer as well as other diseases," concluded co-authors David Nathanson, M.D., and Paul Mischel, M.D., of the David Geffen School of Medicine at UCLA.
The research project was funded by grants from the National Institutes of Health, the National Cancer Institute, the U.S. Department of Defense and MD Anderson's Center for Targeted Therapy; also by awards from the Gillson-Longenbaugh Foundation, AngelWorks, the Marcus Foundation, and the National Foundation for Cancer Research, the Harry S. and Isabel C. Cameron Foundation and the Schissler Foundation.
Other authors are co-first authors Michael Ozawa, Ph.D., and Catherine Moya, Ph.D., both of whose doctoral dissertations emerged from this project, Wouter Driessen, Ph.D., and E. Magda Barbu, Ph.D., of MD Anderson's Koch Center; Hiroyuki Nishimori, M.D., Ph.D., Frank B. Furnari, Ph.D., and Webster K. Cavenee, Ph.D., of the Ludwig Institute for Cancer Research, University of California San Diego; Suren Soghomonyan, Ph.D., Leo G. Flores 2nd, M.D., Ph.D., Vincenzo Paolillo, Ph.D., Mian M. Alauddin, Ph.D., and Juri G. Gelovani, M.D., Ph.D., of MD Anderson's Department of Experimental Imaging; Xiaowen Liang and Magnus Höök, Ph.D., of Texas A&M University Health Science Center, Houston; James P. Basilion, Ph.D., of the Center for Molecular Imaging Research and National Foundation for Cancer Research (NFCR) Center for Molecular Analysis and Imaging, Massachusetts General Hospital; Oliver Bogler, Ph.D., and Frederick Lang Jr., M.D., of MD Anderson's Department of Neurosurgery; and Kenneth Aldape, M.D., and Gregory Fuller, M.D., Ph.D., of MD Anderson's Department of Pathology;
The University of Texas, Arap and Pasqualini have an equity interest in Mercator Therapeutics, which is subject to restrictions under university policy. MD Anderson manages the terms of these arrangements in accordance with its conflict of interest policies.