The role of circular RNA circ_0008285 in gestational diabetes mellitus by regulating the biological functions of trophoblasts

Circular RNAs (circRNAs) has emerged as vital regulator involved in various diseases. In this study, we identified and investigated the potential circRNAs involved in gestational diabetes mellitus (GDM). High-throughput sequencing was used to collect the plasma circRNAs expression profiles of GDM pa...

Full description

Saved in:
Bibliographic Details
Published inBiological research Vol. 54; no. 1; pp. 14 - 12
Main Authors Chen, Haitian, Zhang, Shaofeng, Wu, Yanxin, Li, Zhuyu, Wang, Dongyu, Cai, Shiqin, Wang, Zilian
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 20.04.2021
BioMed Central
Sociedad de Biología de Chile
BMC
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Circular RNAs (circRNAs) has emerged as vital regulator involved in various diseases. In this study, we identified and investigated the potential circRNAs involved in gestational diabetes mellitus (GDM). High-throughput sequencing was used to collect the plasma circRNAs expression profiles of GDM patients. Quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR) was used to measure the expressions of circ_0008285 and circ_0001173 in the plasma specimens. The Pearson's correlation test was employed to assess the correlation between 2 circRNAs expression and the clinicopathologic data. Two circRNAs expression was verified in high glucose (HG)-induced HTR-8/SVneo cells. MTS, transwell assay was used to evaluate the effects of circ_0008285 expression on HG-induced HTR-8/SVneo cells. The network of circ_0008285 was constructed using cytocape. In GDM patients, the expression of circ_0008285 was significantly upregulated, while that of circ_0001173 was decreased. Circ_0008285 was significantly correlated with the total cholesterol and LDL-C levels. Circ_0001173 was significantly correlated with glycated hemoglobin. HG promoted the proliferation, invasion, and migration in HTR-8/SVneo cells, while the knockdown of circ_0008285 exerted reverse effects. In addition, network construction exhibited that circ_0008285 had 45 miRNA binding sites, which correlated with 444 mRNA. circ_0008285 plays an important role and provides a clue for the usage of therapeutic targets in the development of GDM.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0717-6287
0716-9760
0717-6287
DOI:10.1186/s40659-021-00337-3