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Chinese Archives of General Surgery(Electronic Edition) ›› 2017, Vol. 11 ›› Issue (03): 154-158. doi: 10.3877/cma.j.issn.1674-0793.2017.03.003

Special Issue:

• Original Article • Previous Articles     Next Articles

piRNAs derived from GAS5 activating tumor suppressor FOXO4 in breast cancer cell

Xinxin Chen1, Ting Xia1, Xiaowu Hu1, Tengfei Cao1, Lehong Zhang1,()   

  1. 1. Department of Breast Surgery, the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510080, China
  • Received:2016-11-06 Online:2017-06-01 Published:2017-06-01
  • Contact: Lehong Zhang
  • About author:
    Corresponding author: Zhang Lehong, Email:

Abstract:

Objective

To investigate the activation of FOXO4 by piRNAs derived from GAS5 in breast cancer cell.

Methods

A mixture of the five chemically synthesized single-stranded piRNAs, including pi-sno44/74/75/78/81, were transfected into MCF7 cells. Protein expression of FOXO4 and gene expression detected by microarray mRNA, and quantitative analysis of FOXO4 was performed from 29 clinical breast samples.

Results

FOXO4 expression was up-regulated in breast cancer cells, and the up-regulation was related to pi-sno44/74/75/81 (Corr=0.64, 0.91, 0.76, 0.93, P<0.001), but not to pi-sno78 (Corr=0.25, P=0.912).

Conclusion

piRNAs including pi-sno44/74/75/81 derived from GAS5 can mediate the induction of FOXO4, and may lead to the inhibition of tumor growth.

Key words: Breast neoplasms, Microchip analytical procedures, piRNA, FOXO4

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