Down-Regulated miR-21 in Gestational Diabetes Mellitus Placenta Induces PPAR-α to Inhibit Cell Proliferation and Infiltration
This study aimed to investigate the role of expression in the reduction of placental function in GDM patients. qRT-PCR was used to detect the differential expression of in the serum of gestational diabetes mellitus (GDM) and normal pregnant women, and to verify the functional target gene of miR-21 b...
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Published in | Diabetes, metabolic syndrome and obesity Vol. 13; pp. 3009 - 3034 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New Zealand
Taylor & Francis Ltd
01.01.2020
Dove Dove Medical Press |
Subjects | |
Online Access | Get full text |
ISSN | 1178-7007 1178-7007 |
DOI | 10.2147/DMSO.S253920 |
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Summary: | This study aimed to investigate the role of
expression in the reduction of placental function in GDM patients.
qRT-PCR was used to detect the differential expression of
in the serum of gestational diabetes mellitus (GDM) and normal pregnant women, and to verify the functional target gene
of miR-21 by double fluorescence experiments. Cellular experiments were performed to verify the effect of
on cell function.
is down-regulated in the serum and placenta of GDM patients compared to normal pregnant women. In the case of insulin resistance,
knockdown promoted glucose uptake, but no significant effect was found under physiological condition. Functional studies have shown that reduced PPAR
expression can restore miR-21 knockdown-mediated cell growth and metastasis inhibition. Additionally, decreased expression of
but increased expression of
was observed in patients with GDM and GDM rats.
The expression of the placental
, which inhibits cell growth and infiltration by up-regulating
, is downregulated in pregnant GDM patients, which in turn may affect the placental function. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These authors contributed equally to this work |
ISSN: | 1178-7007 1178-7007 |
DOI: | 10.2147/DMSO.S253920 |