Agios Pharmaceuticals, the leading biopharmaceutical company focused on
discovering and developing novel drugs in cancer metabolism, announced
today the publication of a new study that provides further evidence of
the link between a mutated metabolic enzyme and acute myeloid leukemia
(AML), one of the most common types of leukemia in adults. Called an
"oncometabolite" for its role in cancer metabolism, the
2-hydroxyglutarate (2HG) metabolite is produced at high levels by
cancer-associated mutations in an enzyme known as isocitrate
dehydrogenase (IDH). The article, "Idh1-R132H mutation increases murine
hematopoietic progenitors and alters epigenetics," was published in the
July 4, 2012 online edition of the journal Nature.
Lead author and Agios co-founder Tak Mak, Ph.D., director, The Campbell
Family Institute for Breast Cancer Research at Princess Margaret
Hospital, and professor, University of Toronto, in the Departments of
Medical Biophysics and Immunology, said, "This is the first preclinical
model to demonstrate the direct oncogenic effects of an IDH1 mutation in
vivo. This preclinical research sets the stage for the work of
companies like Agios that focus on developing inhibitors to block the
mutated enzyme and prevent the production of this disease-initiating
metabolite."
"This study provides an important step forward in our understanding of
the mechanism of IDH mediated disease," commented David Schenkein, M.D.,
chief executive officer, Agios. "Several years ago, groundbreaking
research by Agios' scientists first established that the mutated
metabolic enzyme IDH1 has acquired a novel activity which produces
extremely high levels of the metabolite 2HG. Today's study provides
important new evidence of the causative link and potential impact of 2HG
on acute leukemia. At Agios, our goal is to develop first-in-class
anticancer drugs that will help patients with cancers driven by these
metabolites. This new research enhances our ability to successfully
develop these medicines."
In the lab, Dr. Mak's team genetically engineered a mouse model carrying
the IDH1 mutation in its blood system. They discovered that the gene
mutation launches a perfect storm - high levels of the oncometabolite
2HG reprograms the blood system to increase the stem cell pool, impairs
the normal bone marrow environment and leads to epigenetic changes
commonly seen in AML. The resulting condition creates a situation
clinically similar to myelodysplastic syndrome - one of the precursors
to this type of leukemia.
The connection between cancer and metabolism has been the focus of
scientists at Agios, who were the first to identify the oncometabolite
in research published in Nature in 2009. The IDH gene
mutation was initially discovered in brain cancers in 2008 by
researchers at Johns Hopkins and subsequently also linked to leukemia.