UC San Diego researcher awarded grant to advance research on chronic lymphocytic leukemia

Oct 15 2013

The Leukemia & Lymphoma Society has awarded Thomas J. Kipps, MD, PhD, Distinguished Professor of Medicine at the University of California, San Diego School of Medicine, with a 5-year, $6.25 million Specialized Center of Research program grant to support research on chronic lymphocytic leukemia (CLL), the most common adult leukemia in the United States.

Kipps, the Evelyn and Edwin Tasch Chair in Cancer Research and UC San Diego Moores Cancer Center deputy director for research, is a recipient of The Leukemia & Lymphoma Society's grant for the "Specific Targets for Therapy of Patients with Chronic Lymphocytic Leukemia," a four-part project. After nearly three decades of investigating and treating CLL, Kipps is considered among the nation's leading experts in the disease. According to the National Cancer Institute, 1 in 192 people will be diagnosed with CLL during their lifetime.

"Although the research proposal is directed toward improving therapy for patients with CLL, the research may impact other leukemias, lymphomas and cancers in general," said Kipps. "The Leukemia & Lymphoma Society's Specialized Center of Research grant plays an important part in moving this research forward."

CLL is a cancer of the blood and bone marrow, characterized by the growth of abnormal white blood cells that ultimately crowd out healthy cells. Treating this slow-growing cancer is challenging because malignant cells are resistant to drugs used to treat other leukemias. Past research has been unable to uncover a common mutation; instead, alterations in CLL occur through different survival pathways.

Kipps and colleagues reported that a protein used by embryo cells during early development, called Receptor-tyrosine-kinase-like Orphan Receptor 1 or ROR1, serves as a switch regulating the spread of cancer, known as metastasis.

The Leukemia & Lymphoma Society grant will permit Kipps to advance the development of potential new therapies that would target identified pathways that support leukemia-cell survival such as ROR1 (Project 1). Because the activation or silencing of one pathway could lead to the expression of another, William Wierda, MD, PhD, of the University of Texas MD Anderson Cancer Center, will take the findings and implement a phase I clinical trial (Project 2).

SOURCE UC San Diego Health System