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Molecular and Cellular Biochemistry

, Volume 351, Issue 1–2, pp 157–164 | Cite as

Endothelial-specific intron-derived miR-126 is down-regulated in human breast cancer and targets both VEGFA and PIK3R2

  • Ni Zhu
  • Dongze Zhang
  • Haoping Xie
  • Zhe Zhou
  • Huyan Chen
  • Tiantian Hu
  • Yuan Bai
  • Yuan Shen
  • Wenjun Yuan
  • Qing Jing
  • Yongwen Qin
Article

Abstract

Endothelial cells are the key components of vascular intima and play pivotal roles in vasculogenesis, angiogenesis, and tumor growth. Using Northern blot and real-time PCR, we confirmed that miR-126 and its host gene EGF-like domain 7 (EGFL7) were widely expressed in rat tissues but strictly expressed in endothelial cells. In mammals, miR-126 gene is embedded in intron7 of EGFL7. To explore the biogenesis of miR-126, plasmid EGFL7(126)-pEGFPc1 containing segment of exon7-intron7-exon8 of EGFL7 was constructed and expressed in 293T. Expression of spliced exon7–8 and excised mature miR-126 was detected by PCR and Northern blot. Knocking-down of endothelial endogenous miR-126 did not affect EGFL7 expression at mRNA or protein level. To investigate the possible roles of miR-126, PicTar, miRBase, miRanda, Bibiserv, and Targetscan were used to screen the targets. VEGFA and PIK3R2 were confirmed as the targets of miR-126 by luciferase reporter assay and Western blot. Interestingly, Northern blot and western blot showed that miR-126 was down-regulated in breast tumors where the VEGF/PI3K/AKT signaling pathway was activated. Introduction of miR-126 mimics into MCF-7 could effectively decrease VEGF/PI3K/AKT signaling activity. In summary, miR-126 was strictly expressed in endothelial cells and excised from EGFL7 pre-mRNA without affecting splicing and expression of its host gene. In addition, miR-126 could target both VEGFA and PIK3R2, and its expression was decreased in human breast cancer, implying that miR-126 may play a role in tumor genesis and growth by regulating the VEGF/PI3K/AKT signaling pathway.

Keywords

MicroRNA EGFL7 VEGFA PIK3R2 Endothelial cell Breast cancer 

Notes

Acknowledgments

This study was supported by the grants from the Major State Basic Research Development Program of the People’s Republic of China (Nos. 2009CB521902, 2009CB521907, 2007CB947002, and 2006CB503807) and the National Natural Science Foundation of China (Nos. 30971231, 30800375, 30670760, and 30570397).

Disclosures

None.

Supplementary material

11010_2011_723_MOESM1_ESM.ppt (343 kb)
Figure. S1 (A) The sequence of miR-126-3p and 5p are highly conserved in human, rat and mouse, fish and chicken. (B) Location of miR-126 in EGFL7 in human, mouse and rat. Figure. S2 Green fluorescence was observed in 293T which were transfected with pEGFPc1-EGFL7(126) (A) and pEGFPc1(B) after 24 h. (C) Luciferase activity was measured in 293T which were co-transfected of PGL3-VEGFA or PGL3-PIK3R2 with pEGFPc1-EGFL7(126) or pEGFPc1. Firefly luciferase was normalized to renilla luciferase. * P < 0.05 compares to controls. (PPT 343 kb)

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Copyright information

© Springer Science+Business Media, LLC. 2011

Authors and Affiliations

  • Ni Zhu
    • 1
  • Dongze Zhang
    • 2
  • Haoping Xie
    • 2
  • Zhe Zhou
    • 2
  • Huyan Chen
    • 2
  • Tiantian Hu
    • 2
  • Yuan Bai
    • 1
  • Yuan Shen
    • 3
  • Wenjun Yuan
    • 2
    • 4
  • Qing Jing
    • 1
  • Yongwen Qin
    • 1
  1. 1.Department of CardiologyChanghai HospitalShanghaiPeople’s Republic of China
  2. 2.Department of Physiology and Key lab of Ministry of Education in Fertility Preservation and MaintenanceNingxia Medical UniversityYinchuanPeople’s Republic of China
  3. 3.Department of Breast SurgeryChanghai HospitalShanghaiPeople’s Republic of China
  4. 4.Department of PhysiologySecond Military Medical UniversityShanghaiPeople’s Republic of China

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