Original Article
Copyright ©2011 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Mar 14, 2011; 17(10): 1276-1285
Published online Mar 14, 2011. doi: 10.3748/wjg.v17.i10.1276
Proteome of human colon cancer stem cells: A comparative analysis
Jian Zou, Xiao-Feng Yu, Zhi-Jun Bao, Jie Dong
Jian Zou, Xiao-Feng Yu, Zhi-Jun Bao, Jie Dong, Department of Gastroenterology, Huadong Hospital, Fudan University, Shanghai 200040, China
Author contributions: Yu XF and Zou J contributed equally to this work; Zou J designed the research; Zou J, Yu XF, Bao ZJ and Dong J performed the majority of experiments; Dong J, Bao ZJ and Zou J analyzed the data; Yu XF and Zou J wrote the paper.
Supported by Medical Guidance Project of Shanghai Science Committee (No. 10411961800) and Youth Science Fund of Fudan University (No. 08FQ49)
Correspondence to: Xiao-Feng Yu, Professor, Department of Gastroenterology, Huadong Hospital, Fudan University, 221 Yanan Xi Road, Shanghai 200040, China. apollozou@hotmail.com
Telephone: +86-21-62483180 Fax: +86-21-62484981
Received: September 2, 2010
Revised: December 10, 2010
Accepted: December 17, 2010
Published online: March 14, 2011
Abstract

AIM: To isolate and identify the biological characteristics of human colon cancer stem cells (SW1116 cells) and further study their proteome.

METHODS: SW1116 cells were isolated and cultured with a serum-free medium (SFM). Sphere formation was assayed to observe the formation of colon cancer stem cell spheres. SW1116 cells were inoculated into a serum-containing medium for observing their differentiation characteristics. Proliferation curve and cross-resistance of SW1116 cells to different drugs were detected by MTT. Percentage of SP cells in SW1116 cells was detected with Hoechst33342 staining. Telomerase activity in SW1116cells was checked by polymerase chain reaction (PCR)-enzyme linked immunosorbent assay. Expressions of stem cell relevant genes and proteins were detected by reverse transcription-PCR and Western blot, respectively. Total protein was isolated from SW1116 cells by two-dimensional gel electrophoresis (2-DE) and differentially expressed proteins were identified by tandem mass spectrometry (MALDI-TOF/TOF).

RESULTS: The isolated SW1116 cells presented as spheroid and suspension growths in SFM with a strong self-renewal, proliferation, differentiation and drug-resistance ability. The percentage of SP cells in SW1116 cells was 38.9%. The SW1116 cells co-expressed the CD133 and CD29 proteins. The telomerase activity in SW1116 cells was increased. The expressions of different stem cell relevant genes and proteins were detected. The proteomic analysis showed that the 26 protein spots were differently expressed in SW1116 cells and 10 protein spots were identified as ubiquitin fusion-degradation 1-like protein, nuclear chloride channel protein, tubulin β, Raichu404X, stratifin, F-actin capping protein α-1 subunit, eukaryotic translation elongation factor 1 delta isoform 2, hypothetical protein, glyceraldehyde-3-phosphate dehydrogenase and guanine nucleotide binding protein β polypeptide 2-like 1, respectively.

CONCLUSION: SW1116 cells are biologically characterized by self-renewal, proliferation and differentiation, and the differently expressed proteins in SW1116 cells may be essential for isolating cancer stem cells.

Keywords: Proteome; Stem cell; Colon cancer; Isolation; Characterization