New Therapeutic Targets in Pancreatic Cancer Developed

p53, the tumor suppressor gene has been identified as new pancreatic cancer target, reveals new study co-led by Steven Leach, MD, Director of Dartmouth's and Dartmouth-Hitchcock's Norris Cotton Cancer Center (NCCC). The study is co-led by //Leach; Omar Abel-Wahab, MD, Associate Member in the Human Oncology and Pathogenesis Program at Memorial Sloan Kettering Cancer Center (MSKCC); and Luisa Escobar-Hoyos, PhD, MSc, Assistant Professor of Therapeutic Radiology at Yale School of Medicine and former post-doc in the Leach laboratory at MSKCC. Dr. Escobar-Hoyos conceived of and performed the work and serves as lead author, while Dr. Leach serves as co-senior author and along with Dr. Abdel-Wahab supervised the work, both while at MSKCC and while at NCCC.

"The most commonly mutated tumor suppressor gene in cancer, p53, dramatically rewires RNA splicing, the fundamental cell mechanism by which RNA is processed before being translated into protein. The rewiring is done in a manner that leads to further activation of the KRAS oncogene, the major 'driver' gene in human pancreatic cancer," explains Leach.

The team analyzed every known mRNA splice variant encoded by the human genome - more than 200,000 possible sequences, in hundreds of pancreatic cancer patients. Their findings, "Altered RNA Splicing by Mutant p53 Activates Oncogenic RAS Signaling in Pancreatic Cancer" are newly published in Cancer Cell. "Our paper shows that a new class of drugs that alter RNA splicing have selective activity against p53-mutant pancreatic cancers," says Leach.

This study shows that there are still fundamental mechanisms to be discovered in cancer that can lead to new treatment strategies. Based on these findings, next steps will be to design clinical trials that will evaluate these new drugs in patients with pancreatic cancer.

Source-Eurekalert