These findings establish the gene as a critical regulator of lung cancer tumor growth. This new information could turn out to be vital for the design of potentially new therapeutic strategies for a group of patients who represent almost half of non-small cell lung cancer cases.
In the study, published online ahead of print by the journal Cancer Research, the scientists found that presence of known oncogene Notch 1 is required for survival of cancer cells. In both cell and animal model studies, disabling Notch 1 leads to a rise in cancer cell death.
“While Notch signaling has emerged as an important target in many types of cancer, current methodologies that target that pathway affect all members of the Notch family, and this has been associated with toxicity,” said Joseph Kissil, a TSRI associate professor who led the study. “We were able to identify Notch 1 as the critical oncogene to target, at least in a common form of lung cancer.”
The new findings show that Notch1 is required for initial tumor growth, as it represses p53, a well-known tumor suppressor protein that has been called the genome’s guardian because of its role in preventing mutations. The p53 protein can repair damaged cells or force them to die through apoptosis—programmed cell death.
Using animal models, the study shows that inhibition of Notch1 signaling results in a dramatic decrease in initial tumor growth. Moreover, disruption of Notch 1 induces apoptosis by increasing p53 stability—substantially increasing its biological half-life, for example.
These findings provide important clinical insights into the correlation between Notch1 activity and the poor prognosis of non-small cell lung cancer patients who carry the non-mutated form of the p53 gene. “If you look at lung cancer patient populations, Notch signaling alone isn’t a prognostic indicator, but if you look at p53-positive patients it is,” Kissil said.
The first author of the study, “Notch1 is Required for Kras-Induced Lung Adenocarcinoma and Controls Tumor Cell Survival via P53” (doi:10.1158/0008-5472.CAN-13-1384), is Silvia Licciulli of TSRI. Other authors include Jacqueline L. Avila, Linda Hanlon and Ellen Pure of The Wistar Institute; Scott Troutman and Smitha Kota of TSRI; Matteo Cesaroni of Temple University School of Medicine, Brian Keith and M. Celeste Simon of the University of Pennsylvania School of Medicine; Fred Radtke of the Ecole Polytechnique Fédérale de Lausanne, Switzerland; and Anthony J. Capobianco of the University of Miami Miller School of Medicine. For more information on the study, see http://cancerres.aacrjournals.org/content/early/2013/08/13/0008-5472.CAN-13-1384.abstract
This research was supported by the National Institutes of Health (grant number CA124495).
About The Scripps Research Institute
The Scripps Research Institute (TSRI) is one of the world’s largest independent, not-for-profit organizations focusing on research in the biomedical sciences. TSRI is internationally recognized for its contributions to science and health, including its role in laying the foundation for new treatments for cancer, rheumatoid arthritis, hemophilia, and other diseases. An institution that evolved from the Scripps Metabolic Clinic founded by philanthropist Ellen Browning Scripps in 1924, the institute now employs about 3,000 people on its campuses in La Jolla, CA, and Jupiter, FL, where its renowned scientists—including three Nobel laureates—work toward their next discoveries. The institute’s graduate program, which awards PhD degrees in biology and chemistry, ranks among the top ten of its kind in the nation. For more information, see www.scripps.edu.
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