Georgia: Led by Georgia State University,
researchers have developed the first robust and noninvasive detection of
early stage liver cancer and liver metastases, in addition to other
liver diseases, such as cirrhosis and liver fibrosis. Their findings were published Wednesday (May 13) in Proceedings of the National Academy of Sciences. More than 700,000 people are diagnosed with liver cancer each
year. It is the leading cause of cancer deaths worldwide, accounting for
more than 600,000 deaths annually, according to the American Cancer Society.
The rate of liver cancer in the U.S. has sharply increased because of
several factors, including chronic alcohol abuse, obesity and insulin
resistance.
“Liver cancers associated with high mortality rates and poor
treatment responses are often diagnosed in the late stages because there
is not a reliable way to detect primary liver cancer and metastasis at a
size smaller than one centimeter,” said Jenny Yang, lead author on the paper, Distinguished University Professor and associate director of the Center for Diagnostics and Therapeutics at Georgia State.
The liver is a common site for a variety of cancers, including
melanoma, breast, pancreatic and colon cancers. Magnetic resonance
imaging (MRI) is the leading imaging technique to detect disease without
using radiation. MRI contrast or imaging agents aid MRI techniques to
obtain tissue-specific images.
As reported by Yang, the applications of MRI contrast agents are not
effective for early detection of cancerous tumors because they are
hampered by uncontrolled blood circulation time, low relaxation rate or
sensitivity, and low specificity. Most contrast agents, she said, are
rapidly excreted from the liver, not allowing sufficient time to obtain
quality imaging.
To more effectively detect cancerous tumors at an early stage,
researchers from Georgia State, in collaboration with researchers from
Emory University, Georgia Tech, the University of Georgia and the
University of Virginia, have developed a new class of protein-based
contrast agents (PRCAs) and an imaging methodology that provides robust
results for the early detection of liver cancer and other liver
diseases.
ProCA32, the researchers’ newly developed contrast agent, allows for
imaging liver tumors that measure less than 0.25 millimeters. The agent
is more than 40 times more sensitive than today’s commonly used and
clinically approved agents used to detect tumors in the liver.
ProCA32 widens the MRI detection window and is found to be essential
for obtaining high-resolution quality images of the liver. This
application has important medical implications for imaging various liver
diseases, the origin of cancer metastasis, monitoring cancer treatment
and guiding therapeutic interventions, such as drug delivery.
“Our new agents can obtain both positive and negative contrast images
within one application, providing double the accuracy and confidence of
locating cancerous tumors,” Yang said. “These agents are also expected
to be much safer with reduced metal toxicity.”
The researchers have shown proof-of-concept that ProCA32 can be used
to detect cancerous liver tumors at an early stage with high
sensitivity. They have also demonstrated that these new agents better
aid the imaging of multiple organs, including the kidney and blood
vessels, in addition to the liver and tumors.
“ProCA32 may have far-reaching implications in the diagnosis of other
malignancies, which in turn would facilitate development of targeted
treatment along with effective monitoring of reduction of tumor burden,”
Yang said. “Our agent and methodology can also be applied to study the
brain and monitor treatment outcomes in a number of disorders, including
stroke and recovery after stroke, Alzheimer’s disease, brain tumors and
gliomas,”
The research is supported by the National Institutes of Health.