US researchers recently announced that a new drug, developed using nanotechnology and a fungus initially contaminated during lab tests, may show broad effectiveness against various types of **cancer**. The drug, named **Lodamin**, was refined over decades, with its development closely linked to the groundbreaking work of cancer expert **Judah Folkman**, who pioneered **angiogenesis therapy**—a treatment approach aimed at cutting off the blood supply to tumors, thereby starving them and stopping their growth.
Lodamin is the result of 20 years of research led by **Volkmann** and his team. In a recent study published in *Nature Biotechnology*, his colleagues highlighted that this angiogenesis inhibitor tablet has shown no significant side effects.
In mouse trials, Lodamin demonstrated effectiveness against multiple types of tumors, including **breast cancer**, **neuroblastoma**, **uterine cancer**, **prostate cancer**, and **brain cancer**. It can help prevent the formation of early-stage tumors and stop the spread of cancerous cells.
One researcher described the results as "clear visible liver." He said, "When I looked at the test group, their livers were almost clearly visible, but you couldn't find the liver of the control mice. They were all covered with tumors."
Lodamin directly targets **tumor cells**, suppressing the growth of **melanoma** and **lung cancer** without causing noticeable side effects. In the experiment, mice that did not receive the drug were fed a regular diet, and their livers became swollen due to tumor growth. In contrast, the livers and spleens of the treated mice remained normal.
After 20 days, 7 out of the 10 untreated mice had died, while all the mice in the test group survived. These findings suggest that Lodamin could be a promising new treatment for several types of cancer, offering hope for more effective and safer therapies in the future.
**Core keywords**: cancer, tumor cells
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