News and Research
Immune System
Researchers Unlock Key Secrets Showing How Tumors Hide
From Immune System
1-8-2004
Tampa, FL (Jan. 8, 2004) -- In one of the biggest advances
to come from the H. Lee Moffitt Cancer Center & Research
Institute in its 16-year history, researchers have unlocked
at least part of the mystery of how tumors flourish undetected
by keeping their presence a secret from sentries of the
body's immune system.
"Flying
beneath the radar" is how Nature Reviews Cancer (http://www.nature.com/cgi-taf/DynaPage.taf?file=/nrc/journal/v4/n1/full/nrc1261_fs.html)
labels the mechanism of tumors evading capture, a process
described by Hua Yu, Ph.D., and her colleagues at Moffitt
and the University of South Florida College of Medicine.
Their findings are published in the current issue of the
journal Nature Medicine.
"Cancer
is allowed to wreak havoc on the body's immune system because
it knows how to fool the body's defensive arsenal,"
explains Jack Pledger, Ph.D., Associate Center Director
for Basic Science and Professor of Biochemistry at USF.
"The discoveries of Dr. Yu give us vital information
about how tumors stay 'invisible.' It opens the way for
new treatments to help flush the cancer cells into the open,
so the body's armies against disease can destroy them."
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Yu is an Associate Professor in the USF Department
of Medical Microbiology and Immunology and the Immunology Program
at Moffitt. Her coauthors on the study include Drew Pardoll, M.D.,
Ph.D., from the Johns Hopkins University School of Medicine, together
with Richard Jove, Ph.D., and William Dalton, Ph.D., M.D., both from
Moffitt and USF. Other authors include Tianhong Wang, Ph.D.., Guilian
Niu, Ph.D., Lyudmila Burdelya, Ph.D., and Marcin Kortylewski, Ph.D.
The study is titled "Regulation of the innate and adaptive immune
responses by Stat3 signaling in tumor cells."
The researchers documented that the tumor's activation
of Stat3 (from the STAT family of proteins that regulates genes) secretes
factors that inhibit the body's immune responses by keeping dendritic
cells from maturing. The activation also blocks expression of inflammatory
mediators required to trigger the immune system.
Other ongoing research at Moffitt related to Stat3
includes using microarray technology to study the characteristic gene
expression profiles or "molecular signatures" of certain
genes that are regulated by the STAT. Scientists suspect that many
genes that are directly or indirectly regulated by Stat3 may contribute
to cancer, and they are working to develop new drugs based on inhibiting
Stat3 for more effective treatment of breast cancer, prostate cancer,
sarcoma, melanoma and other tumors that harbor aberrantly activated
Stat3.
This story has been adapted from a news release issued
by University Of South Florida Health Sciences Center, http://hsc.usf.edu.
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