Richmond, Va. – (May 22, 2012) – Scientists at Virginia Commonwealth University Massey Cancer Center may be one step closer to developing a new therapy for acute myeloid leukemia (AML) after discovering that the targeted agents obatoclax and sorafenib kill leukemia cells much more effectively when combined than when the drugs are administered individually.
Recently published in the journal Blood, the results of a study led by Steven Grant, M.D., Shirley Carter Olsson and Sture Gordon Olsson Chair in Oncology Research, associate director for translational research and program co-leader of Developmental Therapeutics at VCU Massey Cancer Center, and Mohamed Rahmani, Ph.D., associate professor in the Department of Internal Medicine at VCU School of Medicine, showed that the combination of obatoclax and sorafenib synergized to induce a form of cell suicide known as apoptosis and reduced the growth and survival of several types of AML cells while exerting only limited toxicity toward normal, healthy tissues. The results were first obtained in test-tube experiments and were then confirmed by similar findings and extended survival in animal models of AML.
"Prior research suggested that these two drugs may enhance each other's activity as they inhibit complementary survival pathways in leukemia cells," says Grant. "The results of our study are promising. We're looking forward to translating these findings into clinical trials, and we are hopeful we can bring a new, potentially more effective treatment to patients suffering from AML."
Sorafenib is currently approved by the Food and Drug Administration to treat kidney and liver cancers, but recently has been shown to kill a diverse array of malignant cells, including AML cells, particularly those with a specific mutation in a protein known as FLT3. Obatoclax is currently being investigated in clinical trials for various blood cancers.
In AML cells, Grant's team found the combination therapy caused profound cell death and mitochondrial injury, as well as prolonged survival in animal models. Both drugs inhibit the protein Mcl-1, but do so through different mechanisms. Mcl-1 is a protein that has been shown to prevent apoptosis in various cancer cells, and very recently has been shown to play a critical role in the survival of AML cells.
The combination of the two drugs nearly abolished Mcl-1 expression in AML cells, and in doing so unleashed Bax and Bak proteins. Bax and Bak are usually held in check by Mcl-1, and both help initiate apoptosis in cancer cells. Increased levels of Bim were also observed in treated cells. Bim is another pro-apoptotic protein that is often referred to as a "death trigger." Increased levels or activation of all three of these proteins contributed to the pronounced killing of AML cells.
Grant's team also observed protective mechanisms at play in the AML cells. The combination therapy induced autophagy, a process that diverts energy from less critical cellular constituents to enhance survival. Using chloroquine, a drug that suppresses immune responses and is typically used to treat malaria, the researchers were able to inhibit autophagy and increase AML cell death even further.
"When cancer cells are placed under stress, they seek any possible way to remain alive," says Grant. "The combination of these drugs served to block molecular 'escape routes,' leaving the cells no option other than suicide. Thus, it is theoretically possible that a third agent such as chloroquine may enhance the effectiveness of this regimen even further by reducing the cell's ability to induce autophagy."
Moving forward, Grant's team, led by Prithviraj Bose, M.D., assistant professor of internal medicine and hematologist-oncologist at Massey, is proposing a Phase I clinical trial testing this therapy in AML patients. The researchers are working with the involved drug companies, the National Cancer Institute and multiple potential collaborators to initiate the study.
In addition to Rahmani, Grant collaborated on this research with Mandy Mayo Aust and Elisa Attkisson from the Department of Internal Medicine at VCU School of Medicine; and Massey researcher David C. Williams, M.D., Ph.D., and Andrea Ferreira-Gonzalez, Ph.D., from the Department of Pathology at VCU School of Medicine. Funding for this study was provided by Massey as well as by awards CA63753, CA93738, CA100866 and PA50CA130805 from the National Institutes of Health; the Leukemia and Lymphoma Society of America; a Myeloma SPORE award; a Lymphoma SPORE award; and an award from the V Foundation.
About VCU Massey Cancer Center
VCU Massey Cancer Center is one of only 66 National Cancer Institute-designated institutions in the country that leads and shapes America's cancer research efforts. Working with all kinds of cancers, the Center conducts basic, translational and clinical cancer research, provides state-of-the-art treatments and clinical trials, and promotes cancer prevention and education. Since 1974, Massey has served as an internationally recognized center of excellence. It has one of the largest offerings of clinical trials in Virginia and serves patients in Richmond and in four satellite locations. Its 1,000 researchers, clinicians and staff members are dedicated to improving the quality of human life by developing and delivering effective means to prevent, control and ultimately to cure cancer. Visit Massey online at www.massey.vcu.edu or call 877-4-MASSEY for more information.
About VCU and the VCU Medical Center
Virginia Commonwealth University is a major, urban public research university with national and international rankings in sponsored research. Located on two downtown campuses in Richmond, VCU enrolls more than 32,000 students in 211 certificate and degree programs in the arts, sciences and humanities. Sixty-nine of the programs are unique in Virginia, many of them crossing the disciplines of VCU's 13 schools and one college. MCV Hospitals and the health sciences schools of Virginia Commonwealth University compose the VCU Medical Center, one of the nation's leading academic medical centers. For more, see www.vcu.edu.