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Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells

Diallyl disulfide (DADS), the main active component of the cancer fighting allyl sulfides found in garlic, has shown potential as a therapeutic agent in various cancers. Previous studies showed DADS induction of HL‐60 cell differentiation involves down‐regulation of calreticulin (CRT). Here, we inve...

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Autores principales: Sun, Jing, Mu, Hongxiang, Yu, Jia, Li, Linwei, Yan, Hongxia, Li, Guoqing, Tan, Hui, Yang, Nanyang, Yang, Xiaoyan, Yi, Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307788/
https://www.ncbi.nlm.nih.gov/pubmed/30394654
http://dx.doi.org/10.1111/jcmm.13904
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author Sun, Jing
Mu, Hongxiang
Yu, Jia
Li, Linwei
Yan, Hongxia
Li, Guoqing
Tan, Hui
Yang, Nanyang
Yang, Xiaoyan
Yi, Lan
author_facet Sun, Jing
Mu, Hongxiang
Yu, Jia
Li, Linwei
Yan, Hongxia
Li, Guoqing
Tan, Hui
Yang, Nanyang
Yang, Xiaoyan
Yi, Lan
author_sort Sun, Jing
collection PubMed
description Diallyl disulfide (DADS), the main active component of the cancer fighting allyl sulfides found in garlic, has shown potential as a therapeutic agent in various cancers. Previous studies showed DADS induction of HL‐60 cell differentiation involves down‐regulation of calreticulin (CRT). Here, we investigated the mechanism of DADS‐induced differentiation of human leukaemia cells and the potential involvement of CRT and CCAAT enhancer binding protein‐α (C/EBPα). We explored the expression of CRT and C/EBPα in clinical samples (20 healthy people and 19 acute myeloid leukaemia patients) and found that CRT and C/EBPα expressions were inversely correlated. DADS induction of differentiation of HL‐60 cells resulted in down‐regulated CRT expression and elevated C/EBPα expression. In severe combined immunodeficiency mice injected with HL‐60 cells, DADS inhibited the growth of tumour tissue and decreased CRT levels and increased C/EBPα in vivo. We also found that DADS‐mediated down‐regulation of CRT and up‐regulation of C/EBPα involved enhancement of reactive oxidative species. RNA immunoprecipitation revealed that CRT bound C/EBPα mRNA, indicating its regulation of C/EBPα mRNA degradation by binding the UG‐rich element in the 3′ untranslated region of C/EBPα. In conclusion, the present study demonstrates the C/EBPα expression was correlated with CRT expression in vitro and in vivo and the molecular mechanism of DADS‐induced leukaemic cell differentiation.
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spelling pubmed-63077882019-01-04 Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells Sun, Jing Mu, Hongxiang Yu, Jia Li, Linwei Yan, Hongxia Li, Guoqing Tan, Hui Yang, Nanyang Yang, Xiaoyan Yi, Lan J Cell Mol Med Original Articles Diallyl disulfide (DADS), the main active component of the cancer fighting allyl sulfides found in garlic, has shown potential as a therapeutic agent in various cancers. Previous studies showed DADS induction of HL‐60 cell differentiation involves down‐regulation of calreticulin (CRT). Here, we investigated the mechanism of DADS‐induced differentiation of human leukaemia cells and the potential involvement of CRT and CCAAT enhancer binding protein‐α (C/EBPα). We explored the expression of CRT and C/EBPα in clinical samples (20 healthy people and 19 acute myeloid leukaemia patients) and found that CRT and C/EBPα expressions were inversely correlated. DADS induction of differentiation of HL‐60 cells resulted in down‐regulated CRT expression and elevated C/EBPα expression. In severe combined immunodeficiency mice injected with HL‐60 cells, DADS inhibited the growth of tumour tissue and decreased CRT levels and increased C/EBPα in vivo. We also found that DADS‐mediated down‐regulation of CRT and up‐regulation of C/EBPα involved enhancement of reactive oxidative species. RNA immunoprecipitation revealed that CRT bound C/EBPα mRNA, indicating its regulation of C/EBPα mRNA degradation by binding the UG‐rich element in the 3′ untranslated region of C/EBPα. In conclusion, the present study demonstrates the C/EBPα expression was correlated with CRT expression in vitro and in vivo and the molecular mechanism of DADS‐induced leukaemic cell differentiation. John Wiley and Sons Inc. 2018-11-05 2019-01 /pmc/articles/PMC6307788/ /pubmed/30394654 http://dx.doi.org/10.1111/jcmm.13904 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Sun, Jing
Mu, Hongxiang
Yu, Jia
Li, Linwei
Yan, Hongxia
Li, Guoqing
Tan, Hui
Yang, Nanyang
Yang, Xiaoyan
Yi, Lan
Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells
title Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells
title_full Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells
title_fullStr Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells
title_full_unstemmed Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells
title_short Diallyl disulfide down‐regulates calreticulin and promotes C/EBPα expression in differentiation of human leukaemia cells
title_sort diallyl disulfide down‐regulates calreticulin and promotes c/ebpα expression in differentiation of human leukaemia cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307788/
https://www.ncbi.nlm.nih.gov/pubmed/30394654
http://dx.doi.org/10.1111/jcmm.13904
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