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Suppressing Single Protein can Prevent Spread of Pancreatic Cancer

by Kathy Jones on  May 3, 2014 at 10:31 PM Cancer News   - G J E 4
Researchers at Georgetown Lombardi Comprehensive Cancer Center have found that suppressing a single Yap-associated protein can lead to a complete shutdown of the growth of pancreatic cancer, though they admitted that it did not prevent pancreatic cancer from developing in the first place, a new study to be published in the journal Science Signaling reveals.
 Suppressing Single Protein can Prevent Spread of Pancreatic Cancer
Suppressing Single Protein can Prevent Spread of Pancreatic Cancer
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"We believe this is the true Achilles heel of pancreatic cancer, because knocking out Yap crushes this really aggressive cancer. This appears to be the critical switch that promotes cancer growth and progression," says the study's senior investigator, Chunling Yi, PhD, an assistant professor of oncology at Georgetown Lombardi.

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Yi added that because Yap is over-expressed in other cancers, such as lung, liver and stomach tumors, researchers are already working on small molecule drugs that will inhibit activity of the protein and its partnering molecules. The study was conducted in mouse models of pancreatic ductal adenocarcinoma (PDAC), which accounts for all but five percent of human pancreatic cancers. These mice have a mutation in the KRAS gene, as well as a mutation in their p53 gene. "More than 95 percent of pancreatic cancer patients have a KRAS mutation and about 75 percent have a mutation in p53, so these mice provide a natural model of the human disease," she says. Because it has been very difficult to devise drugs that target either KRAS or p53, in this study the researchers looked for other potential druggable targets involved in uncontrolled growth of pancreatic cancer. They found that Yap was over-expressed in both mouse models and human samples of PDAC, and they discovered that the KRAS mutation found in most pancreatic cancer activates Yap. "The KRAS mutation uses Yap to make cancer cells grow, so shutting down Yap defuses the mutated gene's activity," Yi says. Yap also shuts down activity of the p53 oncogene, though the link between p53 and Yap is not yet known. "KRAS and p53 are two of the most mutated genes in human cancers, so our hope is that a drug that inhibits Yap will work in pancreatic cancer patients — who have both mutations — and in other cancers with one or both mutations," Yi says.



Source: Eurekalert
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