TY - JOUR
T1 - Nobiletin suppresses the proliferation and induces apoptosis involving MAPKs and caspase-8/-9/-3 signals in human acute myeloid leukemia cells
AU - Hsiao, Pei Ching
AU - Lee, Wei-Jiunn
AU - Yang, Shun Fa
AU - Tan, Peng
AU - Chen, Hui Yu
AU - Lee, Liang-Ming
AU - Chang, Junn Liang
AU - Lai, Gi-Ming
AU - Chow, Jyh-Ming
AU - Chien, Ming-Hsien
PY - 2014/12/1
Y1 - 2014/12/1
N2 - Nobiletin, a compound isolated from citrus fruits, is a polymethoxylated flavone derivative that was shown to have anti-inflammatory and anticancer activities in various solid tumors. The anticancer effect of nobiletin on nonsolid tumor remains unclear. Herein, the molecular mechanisms by which nobiletin exerts its anticancer effects on acute myeloid leukemia (AML) cells were investigated. The results showed that nobiletin suppressed cell proliferation in various types of AML cell lines. Moreover, nobiletin induced cell-cycle arrest of HL-60 AML cells at the G0/G1 phase by suppressing extracellular signal-regulated kinase (ERK) activity. Furthermore, nobiletin effectively induced apoptosis of HL-60 cells through caspase-8, caspase-9, and caspases-3 activation concomitantly with a marked induction of p38 mitogen-activated protein kinase (MAPK) activation, but without affecting expression levels of Bcl-2, Bax, or Bid. Taken together, our results suggest that nobiletin inhibited HL-60 cell proliferation through inducing cell-cycle arrest and apoptosis and could serve as a potential additional chemotherapeutic agent for treating AML.
AB - Nobiletin, a compound isolated from citrus fruits, is a polymethoxylated flavone derivative that was shown to have anti-inflammatory and anticancer activities in various solid tumors. The anticancer effect of nobiletin on nonsolid tumor remains unclear. Herein, the molecular mechanisms by which nobiletin exerts its anticancer effects on acute myeloid leukemia (AML) cells were investigated. The results showed that nobiletin suppressed cell proliferation in various types of AML cell lines. Moreover, nobiletin induced cell-cycle arrest of HL-60 AML cells at the G0/G1 phase by suppressing extracellular signal-regulated kinase (ERK) activity. Furthermore, nobiletin effectively induced apoptosis of HL-60 cells through caspase-8, caspase-9, and caspases-3 activation concomitantly with a marked induction of p38 mitogen-activated protein kinase (MAPK) activation, but without affecting expression levels of Bcl-2, Bax, or Bid. Taken together, our results suggest that nobiletin inhibited HL-60 cell proliferation through inducing cell-cycle arrest and apoptosis and could serve as a potential additional chemotherapeutic agent for treating AML.
KW - Acute myeloid leukemia
KW - Apoptosis
KW - G/G arrest
KW - Nobiletin
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UR - http://www.scopus.com/inward/citedby.url?scp=84925286068&partnerID=8YFLogxK
U2 - 10.1007/s13277-014-2457-0
DO - 10.1007/s13277-014-2457-0
M3 - Article
C2 - 25164609
AN - SCOPUS:84925286068
SN - 1010-4283
VL - 35
SP - 11903
EP - 11911
JO - Oncodevelopmental Biology and Medicine
JF - Oncodevelopmental Biology and Medicine
IS - 12
ER -