MRI virtual biopsy and treatment of brain metastatic tumors with targeted nanobioconjugates: nanoclinic in the brain.

Abstract

Differential diagnosis of brain magnetic resonance imaging (MRI) enhancement(s) remains a significant problem, which may be difficult to resolve without biopsy, which can be often dangerous or even impossible. Such MRI enhancement(s) can result from metastasis of primary tumors such as lung or breast, radiation necrosis, infections, or a new primary brain tumor (glioma, meningioma). Neurological symptoms are often the same on initial presentation. To develop a more precise noninvasive MRI diagnostic method, we have engineered a new class of poly(β-l-malic acid) polymeric nanoimaging agents (NIAs). The NIAs carrying attached MRI tracer are able to pass through the blood-brain barrier (BBB) and specifically target cancer cells for efficient imaging. A qualitative/quantitative "MRI virtual biopsy" method is based on a nanoconjugate carrying MRI contrast agent gadolinium-DOTA and antibodies recognizing tumor-specific markers and extravasating through the BBB. In newly developed double tumor xenogeneic mouse models of brain metastasis this noninvasive method allowed differential diagnosis of HER2- and EGFR-expressing brain tumors. After MRI diagnosis, breast and lung cancer brain metastases were successfully treated with similar tumor-targeted nanoconjugates carrying molecular inhibitors of EGFR or HER2 instead of imaging contrast agent. The treatment resulted in a significant increase in animal survival and markedly reduced immunostaining for several cancer stem cell markers. Novel NIAs could be useful for brain diagnostic MRI in the clinic without currently performed brain biopsies. This technology shows promise for differential MRI diagnosis and treatment of brain metastases and other pathologies when biopsies are difficult to perform.

• Authors: Rameshwar Patil, Alexander V Ljubimov, Pallavi R Gangalum, Hui Ding, Jose Portilla-Arias, Shawn Wagner, Satoshi Inoue, Bindu Konda, Arthur Rekechenetskiy, Alexandra Chesnokova, Janet L Markman, Vladimir A Ljubimov, Debiao Li, Ravi S Prasad, Keith L Black, Eggehard Holler, Julia Y Ljubimova
• Journal: ACS nano (ACS Nano) Vol. 9 Issue 5 Pg. 5594-608 (May 26 2015) ISSN: 1936-086X [Electronic] United States
• PMID: 25906400 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Nanoconjugates
• Oligonucleotides, Antisense
• ErbB Receptors
• Receptor, ErbB-2

Topics

• Animals
• Base Sequence
• Biopsy (methods)
• Blood-Brain Barrier (metabolism)
• Brain (pathology)
• Brain Neoplasms (diagnosis, genetics, metabolism, pathology)
• Cell Line, Tumor
• Cell Transformation, Neoplastic
• Diagnosis, Differential
• ErbB Receptors (metabolism)
• Female
• Gene Expression Regulation, Neoplastic
• Humans
• Magnetic Resonance Imaging (methods)
• Mice
• Nanoconjugates (chemistry)
• Nanomedicine (methods)
• Neoplasm Metastasis
• Oligonucleotides, Antisense (chemistry, genetics, metabolism)
• Receptor, ErbB-2 (metabolism)
• Survival Analysis