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.
No comments:
Post a Comment