DocumentCode :
3347638
Title :
Notice of Retraction
Alteronol Induces Cycle Arrest in Human Promyelocytic Leukemia (HL-60) Cells
Author :
Ying Yao ; Hongmei Chen ; Ji Chen ; Defang Li ; Bo Zhang ; Yishan Wang ; Zhenhua Wang ; Qiusheng Zheng
Author_Institution :
Key Lab. of Xinjiang Endemic Phytomedicine Resources, Shihezi Univ., Shihezi, 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.

Objective: To investigate the mechanism of inhibition of HL-60 cells proliferation by alteronol in vitro. Methods: Human promyelocytic leukemia (HL-60) cells cultured in vitro were treated with different concentrations of alteronol, Inhibition rate was detected by SRB assay. Cellular morphological changes were observed by AO/EB (acridine orange/ethidium bromide dye) staining. The apoptosis rate was determined by annexin V-FITC/propdium iodide assay. Cell cycle distribution was determined using a Flow Cytometry. Results: The proliferation of HL-60 cells treated with alteronol was inhibited in a dose dependent manner. Based on cell viability assay, observation on cell morphology and apoptosis rate, we confirmed that alteronol played an obvious role in proliferation inhibition in HL-60 cells, but it did not induce apoptosis in HL-60 cells in different concentrations groups. Conclusion: Alteronol could effectively inhibit the proliferation of HL-60 cells by leading to cell cycle arrest in Gl phase.
Keywords :
biochemistry; cellular biophysics; organic compounds; AO-EB staining; HL-60 cell; SRB assay; acridine orange; alteronol; annexin V-FITC/propdium iodide assay; apoptosis rate; cell cycle distribution; cell viability assay; cells proliferation; cellular morphological change; cycle arrest; ethidium bromide dye; flow cytometry; human promyelocytic leukemia cell; inhibition rate; Cancer; Cells (biology); Compounds; Drugs; Humans; In vitro; Morphology;
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.2011.5781648
Filename :
5781648
Link To Document :
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