Induction of miR-21-PDCD4 Signaling by Tungsten Carbide-Cobalt Nanoparticles in JB6 Cells Involves ROS-Mediated MAPK Pathways

Hou, L; Bowman, L; Meighan, TG; Shi, X; Ding, M

HERO ID

1749106

Reference Type

Journal Article

Year

2013

Language

English

PMID

23758151

HERO ID 1749106
In Press No
Year 2013
Title Induction of miR-21-PDCD4 Signaling by Tungsten Carbide-Cobalt Nanoparticles in JB6 Cells Involves ROS-Mediated MAPK Pathways
Authors Hou, L; Bowman, L; Meighan, TG; Shi, X; Ding, M
Journal Journal of Environmental Pathology, Toxicology and Oncology
Volume 32
Issue 1
Page Numbers 41-51
Abstract Tungsten carbide-cobalt (WC-Co) nanoparticle composites have wide applications because of their hardness and toughness. WC-Co was classified as "probably carcinogenic" to humans by the International Agency for Research on Cancer (IARC) in 2003. It is believed that the toxicity and carcinogenesis of WC-Co is associated with particle size. Recent studies demonstrated that the tumor suppressor gene programmed cell death 4 (PDCD4) and its upstream regulator miR-21 have been considered as oncogenes for novel cancer prevention or anticancer therapies. The present study examined the effects of WC-Co nanoparticles on miR-21-PDCD4 signaling in a mouse epidermal cell line (JB6 P+). The results showed that (i) exposure of JB6 cells to WC-Co stimulated a increase of miR-21 generation; (ii) WC-Co also caused inhibition of PDCD4, a tumor suppressor protein and downstream target of miR-21, expression in JB6 cells; (iii) inhibition of ERKs with ERK inhibitor U0126 significantly reversed WC-Cominus;induced PDCD4 inhibition, but inhibition of p38 with p38 inhibitor SB203580 did not; and (iv) ROS scavengers, N-acetyl-L-cysteine and catalase, blocked the inhibitory effect of WC-Co on PDCD4 expression, while superoxide dismutase promoted the inhibitory effect. These findings demonstrate that WC-Co nanoparticles induce miR-21 generation, but inhibit PDCD4 production, which may be mediated through ROS, especially endogenous H2O2, and ERK pathways. Unraveling the complex mechanisms associated with these events may provide insights into the initiation and progression of WC-Co-induced carcinogenesis.
Doi 10.1615/JEnvironPatholToxicolOncol.2013007097
Pmid 23758151
Wosid WOS:000320204100005
Is Certified Translation No
Dupe Override No
Comments Journal: Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer ISSN: 2162-6537
Is Public Yes
Language Text English
Keyword JB6 cells; PDCD4; microRNA 21; nanoparticles; tungsten carbide-cobalt; nanotoxicology; oncogenicity; cell signal pathways; occupational exposure; occupational respiratory disease