Study details complexity of cancer
Sheds light on difficulty of cure
WASHINGTON - Cancer experts who probed every gene in tumors from two of the hardest-to-treat cancers found that cancer is much more complicated than anyone thought - and say they found why a cure is so unlikely after a tumor has spread.
But they also discovered a potential new way to treat a common and fatal form of brain cancer, and opened the door to finding cancer before it has spread, when it can still be cured surgically, they reported yesterday in the journal Science.
"Cancer is very complex - more complex than we had believed," said Dr. Bert Vogelstein of Johns Hopkins University in Baltimore and the Howard Hughes Medical Institute. "It is not going to be easy to develop therapies. If you have 100 patients, you have 100 different diseases."
The findings suggest that popular new targeted therapies such as
A better approach would be to find the pathways - networks of genes - that control a tumor's uncontrolled growth and spread, they told reporters in a telephone briefing.
The international team sequenced the more than 20,000 genes in cells from 24 patients with advanced pancreatic cancer and from 22 patients with glioblastoma multiforme.
The typical pancreatic tumor had 63 genetic mutations, while the average brain tumor had 60, they found.
The good news is they found just 12 pathways that were abnormal in most of the tumors. Some were in expected areas, such as the regulation of programmed cell suicide, or apoptosis, the process by which abnormal cells self-destruct.
"Often what appeared to be mutations in disparate genes turned out to be working in common pathways," said Dr. Kenneth Kinzler of Johns Hopkins, who worked on the study.
One surprising discovery was a new gene called IDH1 found in glioblastoma multiforme, the most common type of brain tumor and one that usually kills patients within a year, said Dr. Victor Velculescu, also of Hopkins.
Massachusetts Senator Edward Kennedy, 76, was diagnosed in May with this type of brain tumor.
The patients with these mutations were younger and lived longer than the typical brain tumor patient.
"Glioblastoma multiformes used to be thought of as one disease," Velculescu told the briefing. "It is now clear they are two."
Vogelstein said the findings suggest pharmaceutical companies should change their approach to developing new cancer drugs.