
Return to the Table of Contents
Jefferson Scientists Find Way to See Breast Cancer Activity from Outside the Body
Using precise, radioactively labeled genetic probes, researchers at Jefferson Medical College have seen cancer gene activity
from outside the body in laboratory mice. The probes, which work by attaching to genetic codes copied from an active cancer
gene, may someday aid physicians and scientists in cancer detection and in determining the appropriate treatment for a cancer.
 |
|
Dr. Wickstrom
|
 |
|
Dr. Thakur
|
“Patients might be able to avoid a great deal of worry and unneeded surgery if cancer gene activity could be detected from
outside the body,” says Eric Wickstrom, PhD, Professor of Biochemistry and Molecular Pharmacology and Microbiology and Immunology
at Jefferson Medical College (JMC) of Thomas Jefferson University and at the Kimmel Cancer Center at Jefferson in Philadelphia.
The scientists would like to detect cancerous breast tumors as early as possible, particularly before they begin to spread
to other areas of the body. “We want to detect them before mammograms can find them,” Dr. Wickstrom says. “We want to see
whether a cancer gene is active, which will tell clinicians the best way to treat it, according to the cancer gene activity
of the tumor. If we can see the hotspot of cancer gene activity before the tumor has formed, we can start to treat earlier.”
The gene, called cyclin D1, is turned on in the majority of breast cancers, he explains. The genetic probe, which is a DNA
derivative, carries an attached radioactive label, and binds to cyclin D1 messenger RNA (mRNA). The latter is involved in
translating DNA instructions and making proteins.
Can Detect Activity of Other Cancer Genes
Dr. Wickstrom, Mathew Thakur, PhD, Professor of Radiology at JMC and their co-workers contend that using genetic probes to
visualize sites of cancer gene activity can work for detecting the activity of other cancer genes in various types of tumors.
“The radioactive probes can help us identify the cancer cells at an early stage,” says Dr. Thakur. “In this technology, we’ve
shown the proof of principle. Several other cancers show characteristic activated genes that we might also be able to use
for early diagnosis, such as pancreatic cancer, prostate cancer and colon cancer.”
According to Dr. Wickstrom, clinical examination and mammography miss almost half of the breast cancers in women under 40,
approximately one-quarter of cancers in women ages 40 to 49 and one-fifth of cancers in women over age 50.
He notes that when suspect lumps are discovered, biopsies are necessary to tell if cancer exists or not. But when such lumps
are removed after suspicious mammograms, two-thirds are found to be benign.
Dr. Wickstrom foresees this particular test for cyclin D1 – which he has used to detect estrogen receptor-positive breast
cancers in mice – eventually being used in medical imaging centers. In addition to a mammogram, a woman could be tested with
a genetic probe – another way, he says, to screen suspicious lumps. It could also be used to detect precancerous zones, as
in ductal carcinoma in situ, and the spread and recurrence of cancer.
The researchers hope to conduct a clinical trial of their probes in suspected cases of breast cancer, and eventually, in other
cancers as well. In the meantime, they reported their results in December in the Journal of Nuclear Medicine, are publishing their results testing for another cancer gene called MYC in January, and are studying other known cancer
genes, such as K-RAS in pancreatic cancer.