Metformin treatment alleviates polycystic ovary syndrome by decreasing the expression of MMP‐2 and MMP‐9 via H19/miR‐29b‐3p and AKT/mTOR/autophagy signaling pathways. Issue 11 (15th April 2019)
- Record Type:
- Journal Article
- Title:
- Metformin treatment alleviates polycystic ovary syndrome by decreasing the expression of MMP‐2 and MMP‐9 via H19/miR‐29b‐3p and AKT/mTOR/autophagy signaling pathways. Issue 11 (15th April 2019)
- Main Title:
- Metformin treatment alleviates polycystic ovary syndrome by decreasing the expression of MMP‐2 and MMP‐9 via H19/miR‐29b‐3p and AKT/mTOR/autophagy signaling pathways
- Authors:
- Chen, Zhilan
Wei, Huafang
Zhao, Xiaoling
Xin, Xin
Peng, Ling
Ning, Yang
Wang, Yapei
Lan, Yanli
Zhang, Qinghua - Abstract:
- Abstract: In this study, we aimed to investigate the molecular pathway(s) underlying the effect of metformin (MET) on the expression of matrix metalloproteinase (MMP)‐2 and MMP‐9. Real‐time polymerase chain reaction, Western blot analysis, and gelatin zymography were used to assay the effects of MET on MMP and AMPK signaling pathways. In addition, HTOG cells were treated with miR‐29b‐3p/a scramble control, H19/a negative control, or MET/PBS to explore possible signaling pathway(s) underlying the inhibitory effect of MET on MMP‐2/MMP‐9. A rat model of polycystic ovary syndrome (PCOS) was also established to validate the molecular mechanism(s) of MET in vivo. The administration of MET suppressed the expression of MMP‐9/MMP‐2 and mTOR while increasing the expression of Akt and AMPK, indicating that MET reduced the expression of MMPs via the AMPK signaling pathway. Meanwhile, the H19/miR‐29b‐3p/MMP‐9 and H19/miR‐29b‐3p/MMP‐2 signaling pathways were implicated in PCOS, in which the interactions between H19/miR‐29b‐3p and MMP‐9/MMP‐2/miR‐29b‐3p were confirmed. Furthermore, the administration of MET suppressed the expression of H19 while elevating the expression of miR‐29b‐3p. And the role of MET in PCOS was also confirmed in vivo via examining the activity of H19 and AMPK signaling pathways in cell or serum samples collected from PCOS rats. MET exhibits a therapeutic effect in the treatment of PCOS by reducing the expression of MMPs. Abstract : The findings of this studyAbstract: In this study, we aimed to investigate the molecular pathway(s) underlying the effect of metformin (MET) on the expression of matrix metalloproteinase (MMP)‐2 and MMP‐9. Real‐time polymerase chain reaction, Western blot analysis, and gelatin zymography were used to assay the effects of MET on MMP and AMPK signaling pathways. In addition, HTOG cells were treated with miR‐29b‐3p/a scramble control, H19/a negative control, or MET/PBS to explore possible signaling pathway(s) underlying the inhibitory effect of MET on MMP‐2/MMP‐9. A rat model of polycystic ovary syndrome (PCOS) was also established to validate the molecular mechanism(s) of MET in vivo. The administration of MET suppressed the expression of MMP‐9/MMP‐2 and mTOR while increasing the expression of Akt and AMPK, indicating that MET reduced the expression of MMPs via the AMPK signaling pathway. Meanwhile, the H19/miR‐29b‐3p/MMP‐9 and H19/miR‐29b‐3p/MMP‐2 signaling pathways were implicated in PCOS, in which the interactions between H19/miR‐29b‐3p and MMP‐9/MMP‐2/miR‐29b‐3p were confirmed. Furthermore, the administration of MET suppressed the expression of H19 while elevating the expression of miR‐29b‐3p. And the role of MET in PCOS was also confirmed in vivo via examining the activity of H19 and AMPK signaling pathways in cell or serum samples collected from PCOS rats. MET exhibits a therapeutic effect in the treatment of PCOS by reducing the expression of MMPs. Abstract : The findings of this study demonstrated that metformin (MET) inhibited the pathogenesis of PCOS by decreasing the expression of matrix metalloproteinase (MMP)‐2 and MMP‐9 via the H19/miR‐29b‐3p and AKT/mTOR/autophagy pathways. In brief, we showed that the administration of MET both activated the AMPK/mTOR/AKT signaling pathway and inhibited H19 expression, which in turn increased the expression of miR‐29b‐3p. As target genes of miR‐29b‐3p, the expression of MMP‐2 and MMP‐9 was inhibited by elevated miR‐29b‐3p expression, thus alleviating the severity of PCOS. … (more)
- Is Part Of:
- Journal of cellular physiology. Volume 234:Issue 11(2019:Nov.)
- Journal:
- Journal of cellular physiology
- Issue:
- Volume 234:Issue 11(2019:Nov.)
- Issue Display:
- Volume 234, Issue 11 (2019)
- Year:
- 2019
- Volume:
- 234
- Issue:
- 11
- Issue Sort Value:
- 2019-0234-0011-0000
- Page Start:
- 19964
- Page End:
- 19976
- Publication Date:
- 2019-04-15
- Subjects:
- Akt -- autophagy -- H19 -- MET -- miR‐29b‐3p -- MMP‐2 -- MMP‐9 -- mTOR -- PCOS
Physiology -- Periodicals
Cell physiology -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcp.28594 ↗
- Languages:
- English
- ISSNs:
- 0021-9541
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.020000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23706.xml