DocumentCode
3324912
Title
Notice of Retraction
ROS and Ca²+ Signal Activator-Resveratrol Induce Human Hepatoma Cancer Cell HepG-2 Apoptosis
Author
An Peng ; Song WenJun
Author_Institution
Biotechnol. & Food Sci. Coll., Tianjin Univ. of Commerce, Tianjin, China
fYear
2011
fDate
10-12 May 2011
Firstpage
1
Lastpage
4
Abstract
Notice of Retraction
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
To study mechanism of resveratrol induce HepG-2 apoptosis via Ca2+ and ROS pathway. Measurements using mononuclear cell direct cytotoxicity assay(the MTT method) shows that its cytotoxic effect on HepG-2 is strong with IC50 being 34.86 μmol·L-1. Measurement of action of apoptosis using morphology show that karyoplasmic ratio of tumor cell become diminish, Cells break up into several apoptotic bodies of different sizes. Measurement rate of apoptosis and cell cycle dealed with RES using flow cytometry shows that RES leads to a decrease in the proportion of cells in G0/G1 phase, an increasement in proportion of cells in S phase and decrease in proportion of cells in G2/M phase. Rates of apoptosis induced by RES are 26.130%, 31.599%, 65.655%. Measurement Ca2+ content in HepG-2 treated with RES using laser scanning confocal microscope with Fluo-3 stain shows that RES can obviously increase Ca2+ content. Measurement content of ROS in HepG-2 treated with RES shows that RES can enhance the content of ROS. RES can induce HepG-2 apoptosis and activate Ca2+ and ROS signaling pathway.
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
To study mechanism of resveratrol induce HepG-2 apoptosis via Ca2+ and ROS pathway. Measurements using mononuclear cell direct cytotoxicity assay(the MTT method) shows that its cytotoxic effect on HepG-2 is strong with IC50 being 34.86 μmol·L-1. Measurement of action of apoptosis using morphology show that karyoplasmic ratio of tumor cell become diminish, Cells break up into several apoptotic bodies of different sizes. Measurement rate of apoptosis and cell cycle dealed with RES using flow cytometry shows that RES leads to a decrease in the proportion of cells in G0/G1 phase, an increasement in proportion of cells in S phase and decrease in proportion of cells in G2/M phase. Rates of apoptosis induced by RES are 26.130%, 31.599%, 65.655%. Measurement Ca2+ content in HepG-2 treated with RES using laser scanning confocal microscope with Fluo-3 stain shows that RES can obviously increase Ca2+ content. Measurement content of ROS in HepG-2 treated with RES shows that RES can enhance the content of ROS. RES can induce HepG-2 apoptosis and activate Ca2+ and ROS signaling pathway.
Keywords
cancer; cellular biophysics; optical microscopy; tumours; Ca2+ signal activator; HepG-2 apoptosis; MTT method; ROS signal activator; direct cytotoxicity assay; flow cytometry; human hepatoma cancer cell; karyoplasmic ratio; laser scanning confocal microscopy; resveratrol; tumor cell; Atmospheric waves; Cancer; DNA; Drugs; Suspensions; Tumors;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioinformatics and Biomedical Engineering, (iCBBE) 2011 5th International Conference on
Conference_Location
Wuhan
ISSN
2151-7614
Print_ISBN
978-1-4244-5088-6
Type
conf
DOI
10.1109/icbbe.2011.5780429
Filename
5780429
Link To Document