Improved model for breast
cancer study may lead to better method for predicting probability
of metastasis
Researchers from Huntsman Cancer Institute
(HCI) at the University of Utah have discovered a new way to model
human breast cancer that could lead to new tools for predicting
which breast cancers will spread and new ways to test drugs that
may stop its spread. Their results are published online in the journal
Nature Medicine.
To create this improved model for breast cancer studies, the researchers
grafted tumor tissue from consenting breast cancer patients directly
into mouse mammary glands, rather than the traditional approach,
where the cancer cells are grown, or cultured, in the laboratory.
They discovered that the grafts remained virtually identical to
the original human breast cancer in structure, genetic makeup and
behavior, unlike the methods that rely on cell cultures.
"The most surprising result was that the tumor grafts spread
from the original site, or metastasized, just as they did in the
human patients," said the study's principal investigator Alana
Welm, Ph.D, assistant professor in the Department of Oncological
Sciences and an HCI investigator. "For example, grafts of tumor
tissue from patients whose cancer had spread to the lung also spread
to the lungs of the mice that received them."
Most breast cancer deaths result from the disease metastasizing
to other areas of the body such as the lymphatic system, lungs,
liver, bones or brain.
In addition, researchers found that the successful grafts were
nearly all from patients who developed the most aggressive forms
of breast cancer and ultimately died of their disease. This result
reveals the modeling method's potential as a tool that, soon after
a breast cancer diagnosis, could identify whether the tumor would
be likely to spread, helping doctors select the best treatment approach
for an individual patient's form of the disease.
"There is also the potential to develop similar models for
other cancers using this method," says Welm. "We are already
working on this with colon cancer tissues."
The study is a cooperative effort of HCI's Breast Disease Oriented
Team, comprised of surgeons, medical and radiation oncologists,
pathologists, and laboratory scientists. Other contributors included
HCI's Comparative Oncology Resource, the Tissue Resource and Application
Core, and ARUP Research Institute. The work was supported by funding
from the U.S. Department of Defense Breast Cancer Research Program,
the American Association for Cancer Research, the Breast Cancer
Research Foundation, and Huntsman Cancer Foundation.
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