Thursday, January 10, 2013

Stony Brook researchers develop new contrast agent

The use of a new brain tumor-targeting contrast agent that differentiates between normal and cancer cells in conjunction with a high-powered microscopy system could potentially lead to a method of more precise neurosurgery for brain tumors, according to research paper published as a cover story in the December issue of Translational Oncology. Developed by researchers in the Department of Biomedical Engineering (BME) at Stony Brook University, the contrast agent adheres to a molecular marker of medulloblastoma, a form of brain cancer, and can be seen by the optical microscope system, also developed by the research team.This page provides information about torch light and how to report a fault.

In their article entitled “Microscopic Delineation of Medulloblastoma Margins in a Transgenic Mouse Model Using a Topically Applied VEGFR-1 Probe,Learn how Laser engraver work and how you benefit from it.” Stony Brook researchers Dr. Jonathan T.Watch and Play model of solar system Planets and Constellations moving over the Night Sky.C. Liu, Assistant Professor of Biomedical Engineering, and BME graduate students Danni Wang, Steven Y. Leigh,The world's leading supplier of residential wind turbines & wind-solar hybrid systems for homes, and Ye Chen, and colleagues from Stanford University, created a contrast agent that adheres to vascular endothelial growth factor receptor 1 (VEGFR-1), which is overexpressed on the surface of many medulloblastoma cell lines and primary tissues. The team developed a VEGFR-1 chemical targeting agent that was topically applied to sample tissue.

Based on the research model, which confirmed cancerous tissue through histopathology,Filipino soldiers install solar bulb through a roof in a shantytown in Manila. the team discovered that by using the contrast agent in conjunction with laser-scanning 3D microscopy, the optical contrast agent caused tumors to “glow” with fluorescence at each of the tumor margins. The process enabled the research team to define tumor margins, including residual tumor cells.

Their approach may have significant implications in the surgical treatment of medulloblastoma because, the authors explain: “Bulk tumor resection remains the first line of treatment, where it has been shown that the completeness of tumor resection correlates strongly with the survival of patients. The goal of neurosurgeons is to maximize the removal of tumor while minimizing the removal of normal tissues.

“The current gold standard for assessing malignancy is histopathology of biopsied tissue samples. However, this is rarely performed at the tumor margins during resection because of the time required for frozen sections to be prepared and interpreted by a pathologist. Furthermore, histopathology is expensive and requires the removal of brain tissue regardless of the state of the tissue.”

“There is a great need for a noninvasive method to rapidly and accurately visualize residual malignancy to assist surgeons during the tumor resection process, and we think that our research results provides a foundation and approach toward that ultimate goal,” said Dr. Liu, Principal Investigator. “Our chemical probe with utilization of a microscope custom-built to view molecular protein biomarkers in three dimensions identifies tumor margins with accuracy that could potentially approach the gold standard of pathology based on tissue biopsies.”

The authors said that next step in the research is to investigate the ability of the VEGFR-1 fluorescent probe, used in conjunction with their microscope and optical system, to enhance surgical resection in experimental models and ultimately in patients.

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