Key result
hEag1 expression in acute myeloid leukemia is linked to a ~42-month decrease in median survival.
Why the study?
Does hEag1 expression predict survival in AML, and does its blockade inhibit AML cell proliferation and migration?
Cohort (n=118)
No
Does hEag1 expression predict survival in AML, and does its blockade inhibit AML cell proliferation and migration?
Absolute Event Rate: 10% vs 52%
p-value: p=0.0019
hEag1 is a novel prognostic factor in AML associated with reduced survival, and its blockade inhibits AML cell proliferation and migration in vitro.
hEag1 expression may refine AML risk stratification; leaves open whether blockade improves outcomes in prospective trials.
BACKGROUND: The voltage-gated potassium channel hEag1 (KV10.1) has been related to cancer biology. The physiological expression of the human channel is restricted to the brain but it is frequently and abundantly expressed in many solid tumors, thereby making it a promising target for a specific diagnosis and therapy. Because chronic lymphatic leukemia has been described not to express hEag1, it has been assumed that the channel is not expressed in hematopoietic neoplasms in general. RESULTS: Here we show that this assumption is not correct, because the channel is up-regulated in myelodysplastic syndromes, chronic myeloid leukemia and almost half of the tested acute myeloid leukemias in a subtype-dependent fashion. Most interestingly, channel expression strongly correlated with increasing age, higher relapse rates and a significantly shorter overall survival. Multivariate Cox regression analysis revealed hEag1 expression levels in AML as an independent predictive factor for reduced disease-free and overall survival; such an association had not been reported before. As a functional correlate, specific hEag1 blockade inhibited the proliferation and migration of several AML cell lines and primary cultured AML cells in vitro. CONCLUSION: Our observations implicate hEag1 as novel target for diagnostic, prognostic and/or therapeutic approaches in AML.
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Agarwal et al. (2010) conducted a cohort in Acute myeloid leukemia (AML) (n=118). hEag1 expression vs. hEag1 negative was evaluated on Median overall survival (months) (p=0.0019). Expression of the hEag1 potassium channel in acute myeloid leukemia was associated with a significantly shorter median overall survival (10 months vs 52 months, p=0.0019) and served as an independent predictive factor for poor outcome.
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