The agent, called KPT-SINE, belongs to a new class of drugs called selective inhibitors of nuclear export (SINE). The agent was developed by Karyopharm Therapeutics Inc. It is designed to kill cancer cells by restoring biochemical pathways that normally cause unhealthy cells to self-destruct through a process called programmed cell death, or apoptosis.
The agent targets a protein called CRM1, which, until now, has not been adequately explored in CLL, the researchers say. During disease progression, cancer cells use CRM1 to shunt certain apoptosis-related proteins out of the nucleus, thereby avoiding cell death.
“We believe that KPT-SINE and other nuclear-export inhibitors may represent a unique, entirely new therapeutic strategy for treating cancer by simultaneously restoring multiple normal cell death pathways,” says OSUCCC – James research scientist Dr. Rosa Lapalombella who is a co-investigator on the study with Dr. John Byrd, director of the division of hematology and co-director of the OSUCCC – James CLL Experimental Therapeutics Laboratory at OSUCCC – James.
The researchers hypothesize that KPT-SINE will inhibit CRM1 and keep these regulatory proteins in the nucleus where they can initiate programmed cell death.
Lapalombella will discuss the role of CRM1 inhibition in the treatment of CLL on Monday, December 12, at 7:45 a.m. during the 53rd Annual Meeting of the American Society of Hematology.
The study, which used CLL cells from patients and a mouse model of CLL, provides essential proof-of-concept data to design and initiate phase I clinical testing of KPT-SINE in patients with these incurable diseases, Lapalombella notes.
“We are excited by our preliminary findings that KPT-SINE represents a promising targeted therapy for CLL patients,” Byrd says. “We look forward to transitioning our research toward early clinical development in patients with CLL and related diseases, based upon the data generated by our team.”
CLL is the most common form of adult leukemia, with about 15,000 new cases annually in the United States. Despite recent therapeutic advancements, all CLL patients will eventually relapse after treatments, and most will die of their leukemia. About 4,400 Americans die of the disease each year.
The Leukemia and Lymphoma Society Translational Research Program, D. Warren Brown Foundation and the Harry T. Mangurian Foundation supported this research.
Other Ohio State researchers involved in the study are Caroline Berglund, Dr. Emilia Mahoney, Katie Williams, Shruti Jha and Dr. Asha Ramanunni.
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute strives to create a cancer-free world by integrating scientific research with excellence in education and patient-centered care, a strategy that leads to better methods of prevention, detection and treatment. Ohio State is one of only 41 National Cancer Institute (NCI)-designated Comprehensive Cancer Centers and one of only seven centers funded by the NCI to conduct both phase I and phase II clinical trials. The NCI recently rated Ohio State’s cancer program as “exceptional,” the highest rating given by NCI survey teams. As the cancer program’s 210-bed adult patient-care component, The James is a “Top Hospital” as named by the Leapfrog Group and one of the top 20 cancer hospitals in the nation as ranked by U.S. News & World Report.
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Contact: Eileen Scahill, Medical Center Public Affairs and Media Relations, 614-293-3737, or Eileen.Scahill@osumc.edu