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Citation
Tags
HERO ID
1247958
Reference Type
Journal Article
Title
Realgar-induced apoptosis of cervical cancer cell line Siha via cytochrome c release and caspase-3 and caspase-9 activation
Author(s)
Cheng, YX; Liu, R; Wang, Q; Li, BS; Xu, XX; Hu, M; Chen, L; Fu, Q; Pu, DM; Hong, L
Year
2012
Is Peer Reviewed?
Yes
Journal
Chinese Journal of Integrative Medicine
ISSN:
1672-0415
EISSN:
1993-0402
Volume
18
Issue
5
Page Numbers
359-365
Language
English
PMID
21526368
DOI
10.1007/s11655-011-0697-z
Web of Science Id
WOS:000303362100007
Abstract
OBJECTIVE:
To explore the molecular mechanism of realgar-induced apoptosis of cervical cancer cells.
METHODS:
The cervical cancer cell line Siha was used to determine the cell viability and apoptosis after treatment with realgar using MTT assay and flow cytometry. The activities of caspase-3, -8, and -9 were detected by fluorescence resonance energy transfer technology and colorimetric assay, while the levels of Bcl-2, cytochrome c, and Bax were detected by Western blot method.
RESULTS:
Induction of apoptosis by realgar was detected in Siha cell line in a dose-dependent manner. The apoptosis was accompanied by a significant increase in cytochrome c release and activation of caspase-3 and caspase-9 but not caspase-8. Further, the realgar-induced apoptosis was inhibited by a broad-spectrum caspase inhibitor, a caspase-3 inhibitor, and a caspase-9 inhibitor but not by a caspase-8 inhibitor. Bcl-2 and Bax protein expressions were not changed by realgar.
CONCLUSION:
The induction of apoptosis by realgar is mediated through a cytochrome c-dependent pathway, which sequentially activates caspase-9 and caspase-3.
Tags
•
Arsenic (Inorganic)
1. Literature
PubMed
4. Adverse Outcome Pathways/Networks Screening
Excluded/Not relevant
Electronic discard
•
Arsenic MOA
2. Electronic Discard
1. MOA Literature Screening
MOA Cluster
•
Inorganic Arsenic (7440-38-2) [Final 2025]
1. Initial Lit Search
PubMed
4. Considered through Oct 2015
6. Cluster Filter through Oct 2015
iAs MOA Literature Categorization
Immune
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