Please wait a minute...

中国生物工程杂志

China Biotechnology
China Biotechnology  2007, Vol. 27 Issue (7): 55-60    DOI:
    
Quantitative and comparative proteomics analysis of gastric cancer and adjacent noncancerous tissues
Download: HTML   PDF(925KB) HTML
Export: BibTeX | EndNote (RIS)      

Abstract  

To identify specific protein markers for gastric cancer detection and diagnosis, as well as develop new potential therapeutic targets of the disease. Gastric cancer tissues and adjacent normal mucosa were examined by the fluorescence differential in-gel electrophoresis (DIGE) technique after labeled with CyDye DIGE fluors Cy3, Cy5 and Cy2. Protein spots detected differential with statistical significance were identified by MALDI-TOF MS or MS/MS. As the result, intensity changes of 33 spots were detected with statistical significance. 9 protein spots of them up-regulated otherwise 24 down-regulated in gastric cancer tissues. And 22 of them were identified by MALDI-TOF MS or MS/MS successfully. Several proteins up-regulated such as MnSOD, HSP60, mutant desmin et al. HSP27, prostaglandin F synthase, SeBP 1, zinc finger protein 160, tubulin alpha 6, eTEF1 A 1 and so on were down-regulated. Our results suggest that DIGE is a useful technique for differential expressed proteins screening and analysis in gastric cancer tissues which may be useful for the development of new molecular markers for diagnosis and prognosis of gastric carcinoma. This differently expressed proteins may be useful tumor markers for gastric cancer.



Key wordsGastric cancer      Tumor marker      Quantitative proteomics     
Received: 10 April 2007      Published: 25 July 2007
Cite this article:

. Quantitative and comparative proteomics analysis of gastric cancer and adjacent noncancerous tissues. China Biotechnology, 2007, 27(7): 55-60.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2007/V27/I7/55

[1] CHEN Xue-yan,ZHANG Na,CHEN Juan,YANG Yan-hong,ZHANG Ju-feng. Effect of Hsa-miR-411-3P on Gastric Cancer Cells and Related Mechanisms[J]. China Biotechnology, 2020, 40(4): 1-9.
[2] Li-peng YAO,Wei GE,Ying-jun HU,Hai-yan LUO,Shan-shan WU,Fei-lei LIN,Jun-ming GUO. The Structural and Functional Characteristics of Circular RNAs and Their Relationships with Gastric Cancer[J]. China Biotechnology, 2018, 38(2): 82-88.
[3] XIN Lin, YANG Wei-feng, ZHANG Hou-ting, LI Yi-fan. Preparation of Folic Acid/chitosan-Prdx6 shRNA Nanoparticles and Its Anti-carcinoma Effect on Gastric Cancer Cell Proliferation[J]. China Biotechnology, 2017, 37(1): 7-13.
[4] LI Ming, WANG Yong-fei, JIAO Jin-xia, YANG Yang, ZHANG Ning, XING Xiang-bin, MA San-mei. The Expression of OPCML in Gastric Cancer and Role of OPCML in Biological Function of Gastric Cancer Cell[J]. China Biotechnology, 2015, 35(2): 1-7.
[5] DENG Meng-yao, CAO Ya. Advances in the Serum Secretome of Cancer[J]. China Biotechnology, 2010, 30(11): 83-87.
[6] HE Ting-Ting, YI Yong-Fen, LI Yan-Jing, XIAO Zhong. Establishment of Proteomics Methods of Golgi Complex Isolated from Gastric Cancer Cells[J]. China Biotechnology, 2010, 30(02): 27-31.
[7] CU Feng, GAO Chun-Fang. Circulating RNA and miRNA in Blood: Potential Applications as Tumor Markers[J]. China Biotechnology, 2009, 29(11): 94-101.
[8] . Phage Display Technology And Its Applications For Tumor Research[J]. China Biotechnology, 2009, 29(09): 0-0.
[9] . Advances in isobaric Tags for Relative and Absolute Quantitation Techniques Research[J]. China Biotechnology, 2006, 26(10): 81-85.