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Chinese Archives of General Surgery(Electronic Edition) ›› 2013, Vol. 07 ›› Issue (06): 431-435. doi: 10.3877/cma.j.issn.1674-0793.2013.06.004

Special Issue:

• Original Article • Previous Articles     Next Articles

Mechanism of insulin promoting absorption of sodium by pancreatic cancer cell SW1990

Ya-dong SONG1, Wen-chao GAO2, Ru-fu CHEN2, Xian-ying HE3, Quan-bo ZHOU2, Qing LIN2, Yu ZHOU2, Bing ZENG4, Min YU2, Zhi-hua LI1,()   

  1. 1. Department of Oncology, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou 510120, China
  • Received:2013-10-23 Online:2013-12-01 Published:2013-12-01
  • Contact: Zhi-hua LI
  • About author:
    Corresponding author: LI Zhi-hua, Email:

Abstract:

Objective

To explain the poor prognosis of new-onset diabetes complicating pancreatic cancer, the impact of insulin on the absorption of sodium by the pancreatic cancer cell (SW1990) was detected.

Methods

The SW1990 cell line cultured in the high glucose DMEM medium was stimulated with insulin of gradient concentration, and the concentrations of Na+ in medium were detected at different time to explore the dose effect and time effect. The impact of insulin on serum and glucocorticoid-inducible kinase 1 (SGK1), and the possible signaling pathways were also studied.

Results

The expression of SGK1 was remarkably increased(P<0.05) while the concentration of Na+ in cell culture solution decreased(P<0.05) after SW1990 was treated with insulin, and the descending range of Na+ was positively related to the SGK1 protein level(r=0.715, P=0.009); the expression of CREBBP and EP300 was closely associated with acetylation elevated apparently after insulin was added(P<0.05).

Conclusion

Insulin can promote the absorption of sodium by the pancreatic cell line, which correlates to the transcription level of SGK1 gene, and acetylation may play a role in this process.

Key words: Insulin, Pancreatic cancer, Diabetes mellitus, Sodium, SGK1, Acetylation

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