Newly
identified proteins similar to prostate-specific antigen show potential
as biomarkers for ovarian cancer
Newly identified members of the enzyme
family that includes prostate-specific antigen show promise as potential
biomarkers for ovarian cancer, according to a presentation at the
annual meeting of the American Association of Clinical Chemistry.
The kallikreins are a subgroup of an enzyme family called serine
proteases. Kallikreins are expressed widely in the body, especially
in hormone dependent tissues such as those of the testes, ovaries,
and breast.
In the current work, Canadian researchers
led by Eleftherios P. Diamandis, M.D., Ph.D, showed that newly identified
members of the human kallikrein family -- such as hK5, hK6, hK7,
hK8, hK10, and hK11 ? have promise as biomarkers for ovarian cancer.
The research group had hypothesized that the newly identified proteins
make up an enzyme cascade that is overexpressed in ovarian cancer
cells, resulting in elevated levels of the enzymes that are part
of the cascade.
The team examined serum samples collected
5 to 10 years ago from women with advanced-stage ovarian cancer.
The medical history included clinical information such as stage,
grade, and survival rate. Investigators correlated the levels of
certain kallikreins with clinical pathological findings and found
that many of the kallikreins that were abundant in the blood samples
were associated with unfavorable prognostic markers such as advanced-stage
or higher-grade disease. The researchers also discovered that patients
who had higher elevations had shorter overall survival than those
who had no elevation.
A current screening procedure using
a biomarker called CA125 and ultrasound examination shows low sensitivity
in detecting early-stage disease; Diamandis believes research on
kallikrein expression patterns in women with early-stage disease
may result in identification of biomarkers that can be used in combination
with the current screening technique to diagnose the disease before
it has become widespread.
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