Home: Publications: Forum Archives: MFF Forum, edition 4
Research
Update: DNA Arrays Diagnose, Predict Survival for Sézary Syndrome
Louise C. Showe, Ph.D., of
the Wistar Institute in Philadelphia, Pennsylvania, has recently reported
the use of DNA array technology to identify important genes involved
in Sézary syndrome. DNA arrays provide scientists with the ability
to assess the activity of thousands of different genes and determine
which genes are turned on or off in any particular tissue studied.
Dr. Showe utilized customized DNA arrays to analyze 4,500 genes and
identified 385 genes that were either overactive or underactive in
blood samples taken from the 45 Sézary syndrome patients, as
compared to 20 normal controls.
Studying the activity of only
eight of the 385 genes permitted investigators to accurately diagnose
Sézary syndrome in patients with as low as five percent abnormal
(Sézary) cells circulating in their blood. A panel of ten genes
appeared to provide prognostic information, as it predicted a subset
of patients that died of their disease within six months, regardless
of their tumor burden. And one gene was seen to occur in about 70 percent
of the Sézary patients but never in the controls, making it
a highly specific marker for the malignant cells.
The research project was a
collaborative effort between Dr. Showe and cutaneous T-cell lymphoma
(CTCL) investigators Dr. Eric C. Vonderheid of Johns Hopkins University
Medical Center and Dr. Alain H. Rook of the University of Pennsylvania
Medical Center. Their work is reported in the June 2 issue of the Journal
of Experimental Medicine and was supported by a research grant from
the National Institutes of Health (NIH). With continued NIH funding,
Dr. Showe plans to extend her collaborative work and study skin samples
from patients with CTCL.
This research builds a foundation
to identify genetic markers that will more accurately diagnose and
predict the course of CTCL that, in the future, may help guide clinicians
weighing treatment options for their patients. In addition, each of
the genes identified may be a potential target for drug development,
greatly expanding the field of possibility for future treatments.
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