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17 April 2014 12:48 pm ,
Vol. 344 ,
Officials last week revealed that the U.S. contribution to ITER could cost $3.9 billion by 2034—roughly four times the...
An experimental hepatitis B drug that looked safe in animal trials tragically killed five of 15 patients in 1993. Now,...
Using the two high-quality genomes that exist for Neandertals and Denisovans, researchers find clues to gene activity...
A new report from the Intergovernmental Panel on Climate Change (IPCC) concludes that humanity has done little to slow...
Astronomers have discovered an Earth-sized planet in the habitable zone of a red dwarf—a star cooler than the sun—500...
Three years ago, Jennifer Francis of Rutgers University proposed that a warming Arctic was altering the behavior of the...
- 17 April 2014 12:48 pm , Vol. 344 , #6181
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New Cancer Therapy Kills Blood Vessels
1 October 2001 7:00 pm
Like all animal tissues, cancerous tumors need blood to survive, and one of the hottest areas in cancer research is finding ways to block that blood supply. Now scientists have created a new therapy that destroys the blood vessels feeding tumors in mice, while leaving other blood vessels unharmed. Scientists say that the findings could eventually lead to new cancer therapies in humans.
Cancer researchers had high hopes when scientists reported in 1997 that two new drugs, angiostatin and endostatin, had prevented blood vessel growth and dramatically shrunk tumors in mice. Several of these so-called antiangiogenesis drugs are in clinical trials, and early results look promising. But these drugs all share a major drawback: Although they stop or slow tumor growth, they don't destroy existing blood vessels on the tumor. This ought to be possible because the inner walls of tumor vessels are covered with a protein called tissue factor (TF) not present in normal blood vessels.
Yale University biochemists Zhiwei Hu and Alan Garen exploited this discrepancy to create a new drug that seeks out tumor blood vessels and destroys them. The drug, known as icon, is a single compound consisting of two parts, one that recognizes blood vessels coated with TF and another that provokes the immune system to attack them. The researchers theorized that these two components together should attack tumor vessels without harming normal ones. To test icon, they injected a virus genetically engineered to produce it into seven mice with human prostate cancer.
In the 2 October early edition of the Proceedings of the National Academy of Sciences, they report that the tumors in the mice steadily shrank over about 200 days with only a small sliver remaining at the end of the experiment. In contrast, the tumors in seven control mice grew rapidly and they died within 63 days. The therapy was effective against human melanoma tumors in mice as well, and the scientists think that it can fight a broad range of cancers.
Harvard cancer biologist Judah Folkman, who studies antiangiogenesis drugs, says the researchers' "novel and elegant" approach may lead to new therapies that can be tested for human cancers. "This is a very important paper," Folkman says.