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Het kruid Zoete Alsem tegen kanker*
Onderzoekers van de universiteit van Washington hebben op basis van het kruid zoete alsem een stof ontwikkeld die wel 1.200 keer beter bepaalde kankercellen kan doden dan de bestaande medicijnen die gebruikt worden bij een chemotherapie. Uit laboratoriumtests blijkt dat zowel leukemiecellen als prostaatkanker- en borstkankercellen gedood kunnen worden. Het kruid zoete alsem (Artemisia annua) wordt al duizenden jaren als medicijn gebruikt in China en in verschillende Aziatische landen bij salades gegeten. Normaal geeft een chemotherapie nogal wat bijwerkingen waarbij zelfs verschillende patiŽnten overlijden als gevolg van deze therapie. De oorzaak zit hem in het gegeven dat de medicijnen bij een chemotherapie ook gezonde cellen doden en wel in een verhouding van 1 op 5-10 kankercellen. De bioactieve stof artemisinine in zoete alsem maakt gebruik van de grote hoeveelheden ijzer in kankercellen. Samen met ijzer is artemisinine zeer giftig voor een cel waardoor deze gedood wordt. Dit is het grote voordeel van artemisinine omdat bijna alle kankercellen afhankelijk zijn van ijzer. Zo doet artemisinine wel 100 kankercellen doden en slechts 1 gezonde cel. Zoete alsem alleen is dus al 10-20 keer effectiever dan de medicijnen die gebruikt worden bij een chemokuur en dat zonder bijwerkingen. De stof die op basis van zoete alsem gemaakt is en wel 1.200 keer effectiever is zal nu verder getest worden.
New Cancer-Killing Compound Developed From Salad Plant
Researchers at the University of Washington have updated a traditional Chinese medicine to create a compound that is more than 1,200 times more specific in killing certain kinds of cancer cells than currently available drugs, heralding the possibility of a more effective chemotherapy drug with minimal side effects. 
The new compound puts a novel twist on the common anti-malarial drug artemisinin, which is derived from the sweet wormwood plant (Artemisia annua L). Sweet wormwood has been used in herbal Chinese medicine for at least 2,000 years, and is eaten in salads in some Asian countries. 
The scientists attached a chemical homing device to artemisinin that targets the drug selectively to cancer cells, sparing healthy cells. The results were published in the journal Cancer Letters. 
"The compound is like a special agent planting a bomb inside the cell," said Tomikazu Sasaki, chemistry professor at UW and senior author of the study. 
In the study, the UW researchers tested their artemisinin-based compound on human leukemia cells. It was highly selective at killing the cancer cells. The researchers also have preliminary results showing that the compound is similarly selective and effective for human breast and prostate cancer cells, and that it effectively and safely kills breast cancer in rats, Sasaki said. 
Cancer drug designers are faced with the unique challenge that cancer cells develop from our own normal cells, meaning that most ways to poison cancer cells also kill healthy cells. Most available chemotherapies are very toxic, destroying one normal cell for every five to 10 cancer cells killed, Sasaki said. This is why chemotherapy's side effects are so devastating, he said. 
"Side effects are a major limitation to current chemotherapies," Sasaki said. "Some patients even die from them." 
The compound Sasaki and his colleagues developed kills 12,000 cancer cells for every healthy cell, meaning it could be turned into a drug with minimal side effects. A cancer drug with low side effects would be more effective than currently available drugs, since it could be safely taken in higher amounts. 
The artemisinin compound takes advantage of cancer cell's high iron levels. Artemisinin is highly toxic in the presence of iron, but harmless otherwise. Cancer cells need a lot of iron to maintain the rapid division necessary for tumor growth. 
Since too much free-floating iron is toxic, when cells need iron they construct a special protein signal on their surfaces. The body's machinery then delivers iron, shielded with a protein package, to these signals proteins. The cell then swallows this bundle of iron and proteins. 
Artemisinin alone is fairly effective at killing cancer cells. It kills approximately 100 cancer cells for every healthy cell, about ten times better than current chemotherapies. To improve those odds, the researchers added a small chemical tag to artemisinin that sticks to the "iron needed here" protein signal. The cancer cell, unaware of the toxic compound lurking on its surface, waits for the protein machinery to deliver iron molecules and engulfs everything - iron, proteins and toxic compound. 
Once inside the cell, the iron reacts with artemisinin to release poisonous molecules called free radicals. When enough of these free radicals accumulate, the cell dies. 
"The compound is like a little bomb-carrying monkey riding on the back of a Trojan horse," said Henry Lai, UW bioengineering professor and co-author of the study. 
The compound is so selective for cancer cells partly due to their rapid multiplication, which requires high amounts of iron, and partly because cancer cells are not as good as healthy cells at cleaning up free-floating iron. 
"Cancer cells get sloppy at maintaining free iron, so they are more sensitive to artemisinin," Sasaki said. 
Cancer cells are already under significant stress from their high iron contents and other imbalances, Sasaki said. Artemisinin tips them over the edge. The compound's modus operandi also means it should be general for almost any cancer, the researchers said. 
"Most currently available drugs are targeted to specific cancers," Lai said. "This compound works on a general property of cancer cells, their high iron content." 
The compound is currently being licensed by the University of Washington to Artemisia Biomedical Inc., a company Lai, Sasaki and Narendra Singh, UW associate professor of bioengineering, founded in Newcastle, Wash. for development and commercialization. Human trials are at least several years away. Artemisinin is readily available, Sasaki said, and he hopes their compound can eventually be cheaply manufactured to help cancer patients in developing countries. 
Other authors of the study are Steve Oh, UW medical student; Byung Ju Kim, UW chemistry instructor; and Singh. 
The Washington Technology Center and the Witmer Foundation provided funding for the study. 
Source: Rachel Tompa 
University of Washington (
December 2008)


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