Imagine a drug which can kill tumors of any kind and you have what  researchers are only steps away from knowing. It is the antibody drug, CD47,  which has been found to have more impact than previously thought  against cancers of the blood. Recently, researchers and scientists at  the Stanford University School of Medicine in Palo Alto, California have  performed a series of tests on mice with successful results. The data from these tests helped  scientists to determine whether to move forward with new human trials.
 Dr. Irving Weissman, Stanford professor of Pathology and the lead  study author is hopeful that there is enough data from the mice trials.  Weissman told Science Now that, “what we’ve shown is that CD47 isn't just important on leukemias  and lymphomas. It’s on every single human primary tumor that we tested.”  It was found that cancer cells always ended up having higher levels of  CD47 than the healthy cells. The question then is whether a CD47 tumor  can predict the odds of survival for patients.
 Research was conducted on mice with seven different types of cancer tumors: Breast, ovary,  colon, liver, brain, prostrate, and bladder. The findings were then  published in the Proceedings of the National Academy of Science.  Weissman and his team are preparing for phase I human trials, which will  be funded by a four year, $20 million grant from the California  Institute for Regenerative Medicine.
 While the research and findings may be substantial evidence to move  forward with human trials, there are some who warn against jumping to  conclusions in findings. As Science Now reported,  cancer researcher Tyler Jacks of the MIT notes that while the study is  promising, more research should still be conducted to see whether humans  will react in the same way. Jacks said that "It’s possible that a real  tumor has additional immune suppressing effects." Another question Jacks  poses is how the CD47 antibodies would complement existing treatments.  Trials will move forward, however with data that has been found and  analyzed.
 Weissman noted, "We have enough data already … that I can say I’m confident that this will move to phase I human trials."
 
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