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Epigenetic Inactivation of the Circadian Clock Gene BMAL1 in Hematologic Malignancies
Cancer Research, 11/03/09
Taniguchi H et al. – The DNA hypermethylation–associated loss of BMAL1 also prevents the recruitment of its natural partner, the CLOCK protein, to their common targets, further enhancing the perturbed circadian rhythm of the malignant cells. These findings suggest that BMAL1 epigenetic inactivation contributes to the development of hematologic malignancies by disrupting the cellular circadian clock.
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