Open AccessCurcumin Blocks Kv11.1 (<i>erg</i>) Potassium Current and Slows Proliferation in the Infant Acute Monocytic Leukemia Cell line THP-1
Author(s) -
Umberto Banderali,
Darrell D. Belke,
Anjali Singh,
Aarthi Jayanthan,
Wayne R. Giles,
Aru Narendran
Publication year - 2011
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000335850
Subject(s) - thp1 cell line , cell growth , curcumin , myeloid leukemia , cell culture , leukemia , potassium channel , microbiology and biotechnology , monocytic leukemia , haematopoiesis , intracellular , cancer research , chemistry , stem cell , biology , medicine , pharmacology , immunology , biochemistry , genetics
Acute Myeloid Leukemia (AML) accounts for approximately one fifth of all childhood leukemia yet is responsible for a significant proportion of morbidity and mortality in this population. For this reason, research to identify novel targets for the development of effective AML therapeutics has intensified in the recent past. The THP-1 cell line, which was originally established from an infant diagnosed with AML, provides an experimental model for functional, pre-clinical therapeutics and target identification studies of AML. Here we show the expression of the voltage gated potassium channel Kv11.1 in THP-1 cells as opposed to normal hematopoietic stem cells. In addition, curcumin, a natural polyphenol derived from the plant Curcuma longa, effectively blocked Kv11.1 activity and also inhibited the proliferation of these cells. Curcumin was rapidly internalized by THP-1 cells and possibly exerts potential growth inhibitory activity by interacting with intracellular epitopes of the ion channel. Inhibition of ionic currents carried by Kv11.1 resulted in depolarization of cell membrane potential. We propose that the inhibition of Kv11.1 activity by curcumin may lead to interference with leukemic cell physiology and consequently the suppression of survival and proliferation of AML cells.