The molecular mechanisms and gene expression profiling for shikonin-induced apoptotic and necroptotic cell death in U937 cells

Jin Lan Piao, Zheng Guo Cui, Yukihiro Furusawa, Kanwal Ahmed, Mati Ur Rehman, Yoshiaki Tabuchi, Makoto Kadowaki, Takashi Kondo

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Shikonin (SHK), a natural naphthoquinone derived from the Chinese medical herb Lithospermum erythrorhizon, induces both apoptosis and necroptosis in several cancer cell lines. However, the detailed molecular mechanisms involved in the initiation of cell death are still unclear. In the present study, caspase-dependent apoptosis was induced by SHK treatment at 1 μM after 6 h in U937 cells, with increase in DNA fragmentation, generation of intracellular reactive oxygen species (ROS), fraction of cells with low mitochondrial membrane potential (MMP), and in the expression of BH3 only proteins Noxa and tBid. Interestingly, caspase-independent cell death was also detected with SHK treatment at 10 μM, observed as increase in SYTOX® Green staining and release of lactate dehydrogenase (LDH). Necrostatin-1 (Nec-1) completely inhibited the SHK-induced leakage of LDH and SYTOX® Green staining. Cell permeable exogenous glutathione (GSH) completely inhibited 1 μM SHK-induced apoptosis and converted 10 μM SHK-induced necroptosis to apoptosis. Gene expression profiling revealed that 353 genes were found to be significantly regulated by 1 μM and 85 genes by 10 μM of SHK treatment, respectively. Among these genes, the transcription factor 3 (ATF3) and DNA-damage-inducible transcript 3 (DDIT3) were highly expressed at 1 μM of SHK treatment, while tumor necrosis factor (TNF) expression mainly increased at 10 μM treatment. These findings provide novel information for the molecular mechanism of SHK-induced apoptosis and necroptosis.

Original languageEnglish
Pages (from-to)119-127
Number of pages9
JournalChemico-Biological Interactions
Volume205
Issue number2
DOIs
Publication statusPublished - 2013

Fingerprint

U937 Cells
Gene Expression Profiling
Cell death
Gene expression
Cell Death
Apoptosis
Genes
Caspases
L-Lactate Dehydrogenase
BH3 Interacting Domain Death Agonist Protein
Lithospermum
Transcription Factor 3
Noxae
Staining and Labeling
Naphthoquinones
shikonin
Mitochondrial Membrane Potential
DNA
DNA Fragmentation
DNA Damage

Keywords

  • Apoptosis
  • Gene expression
  • Necroptosis
  • Shikonin

ASJC Scopus subject areas

  • Toxicology

Cite this

The molecular mechanisms and gene expression profiling for shikonin-induced apoptotic and necroptotic cell death in U937 cells. / Piao, Jin Lan; Cui, Zheng Guo; Furusawa, Yukihiro; Ahmed, Kanwal; Rehman, Mati Ur; Tabuchi, Yoshiaki; Kadowaki, Makoto; Kondo, Takashi.

In: Chemico-Biological Interactions, Vol. 205, No. 2, 2013, p. 119-127.

Research output: Contribution to journalArticle

Piao, Jin Lan ; Cui, Zheng Guo ; Furusawa, Yukihiro ; Ahmed, Kanwal ; Rehman, Mati Ur ; Tabuchi, Yoshiaki ; Kadowaki, Makoto ; Kondo, Takashi. / The molecular mechanisms and gene expression profiling for shikonin-induced apoptotic and necroptotic cell death in U937 cells. In: Chemico-Biological Interactions. 2013 ; Vol. 205, No. 2. pp. 119-127.
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