WEDNESDAY, June 29 (HealthDay News) -- In the largest such study
of any tumor type to date, scientists say they've gleaned an
in-depth look at genes that may help drive aggressive ovarian
The achievement, which could lead to a better understanding of
this "silent killer" and ways to treat it, comes as part of The
Cancer Genome Atlas (TCGA) Research Network. That project was
launched in 2006 by the U.S. National Cancer Institute and the U.S.
National Human Genome Research Institute.
"We have now a map that is telling the cancer research community where to look and what to work on in the future," explained study lead author Paul T. Spellman, who conducted his research while a staff scientist at the Lawrence Berkeley National Laboratory in Berkeley, Calif. "The public should know that this is not an answer in itself. But before this we were essentially making guesses. Now we actually have a very good road map."
The findings are published in the June 30 issue of
According to the American Cancer Society, ovarian cancer is the
fifth most common cancer among women, but it is especially lethal
because it is often caught too late for effective treatment. Nearly
14,000 American women died of ovarian cancer in 2010, the cancer
The new genomic research looked specifically at high-grade
serous ovarian adenocarcinoma (HGS-OvCa), the most common form of
the disease, which accounts for roughly 85 percent of all ovarian
cancer deaths. Looking at 316 tumors, the researchers focused on
what's called "whole-exome sequencing," examining those regions of
the genome that deal with protein production. These types of
examinations, along with others, were also conducted on another 173
ovarian tumor specimens.
"This battery of analyses is a big step up in characterizing the many different kinds of changes that can cause cancer, in this case ovarian cancer," Spellman explained.
Among some of the main findings:
The genomic scan also points to tantalizing new leads for
potential treatments, the researchers said.
For example, mapping also revealed 68 genes that could become
appropriate therapeutic targets for medications -- either drugs
already approved for cancer treatment by the U.S. Food and Drug
Administration or drugs still under development, the researchers
According to the team, as many as half of all the aggressive
ovarian tumors they studied might respond to drugs that focus on
genetic weaknesses in the tumor to help induce cancer cell
Dr. Andrew Berchuck, director of the gynecologic cancer program
at Duke Cancer Institute in Durham, N.C., said that the main point
here is that "not all ovarian cancers are alike."
"What's basically been done here is an autopsy," he explained. "A forensic analysis of tumors. And what they find is that the molecular changes that occur in one case of ovarian cancer can be dramatically different from that of another in terms of what's gone wrong in terms of cell growth and cell death," he added.
"This was suspected to be the case," said Berchuck, who is also a member of the TCGA ovarian cancer working group, and a spokesperson for the Foundation for Women's Cancer. But, "no one's ever mapped it out in extraordinary detail like this before, so that we can begin to understand the biology and root causes of what's going on," he pointed out.
"For patients, what's important is that we can now look at an individual cancer and characterize the molecular alterations that have caused that specific cancer to arise," Berchuck said. "And then those alterations become therapeutic targets for treating that particular cancer. So it really ushers in the potential for personalized medicine, in which you're not treating all ovarian cancers in the same way. Of course, it's a big leap between that knowledge and being able to do something about it. But this represents a major step in the right direction."
For more on ovarian cancer, visit the
U.S. National Institutes of Health.
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