The combination of oolonghomobisflavan B and diallyl disulfide induces apoptotic cell death via 67-kDa laminin receptor/cyclic guanosine monophosphate in acute myeloid leukemia cells

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Title
The combination of oolonghomobisflavan B and diallyl disulfide induces apoptotic cell death via 67-kDa laminin receptor/cyclic guanosine monophosphate in acute myeloid leukemia cells
Author(s)
Jaehoon Bae; Su-Jin Park
Bibliographic Citation
Current Issues in Molecular Biology, vol. 46, no. 3, pp. 2444-2455
Publication Year
2024
Abstract
Diallyl disulfide (DADS) is a well-known principal functional component derived from garlic (Allium sativum) that has various health benefits. Previously, we identified a 67-kDa laminin receptor, a receptor for oolong tea polyphenol oolonghomobisflavan B (OHBFB). However, its molecular mechanisms still remain to be elucidated. Here, we show that DADS synergistically enhanced the effect of the oolong tea polyphenol oolonghomobisflavan B (OHBFB), which induces apoptosis in acute myeloid leukemia (AML) cancer cells without affecting normal human peripheral blood mononuclear cells (PBMCs). The underlying mechanism of OHBFB-induced anti-AML effects involves the upregulation of the 67-kDa laminin receptor/endothelial nitric oxide synthase/cyclic guanosine monophosphate (cGMP)/protein kinase c delta (PKCδ)/acid sphingomyelinase (ASM)/cleaved caspase-3 signaling pathway. In conclusion, we show that the combination of OHBFB and DADS synergistically induced apoptotic cell death in AML cells through activation of 67LR/cGMP/PKCδ/ASM signaling pathway. Moreover, in this mechanism, we demonstrate DADS may reduce the enzyme activity of phosphodiesterase, which is a negative regulator of cGMP that potentiates OHBFB-induced AML apoptotic cell death without affecting normal PBMCs.
Keyword
Oolonghomobisflavan BDiallyl disulfideAcute myeloid leukemiaCyclic guanosine monophosphateAcid sphingomyelinase
ISSN
1467-3037
Publisher
MDPI
Full Text Link
http://dx.doi.org/10.3390/cimb46030154
Type
Article
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
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