4.6 Article

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

Journal

BIOLOGICAL RESEARCH
Volume 54, Issue 1, Pages -

Publisher

SOC BIOLGIA CHILE
DOI: 10.1186/s40659-021-00337-3

Keywords

Circular RNA; Gestational diabetes mellitus; circ_0008285; Functional analysis

Categories

Funding

  1. National Key R&D Program of China [2018YFC1002900]
  2. Natural Science Foundation of Guangdong Province, China [2015A030313198]
  3. Youth Cultivation Project of Sun Yat-sen University, China [17ykpy24]
  4. National Natural Science Foundation of China [81771606, 81571452]

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In this study, circRNAs were identified in gestational diabetes mellitus (GDM) patients, with circ_0008285 upregulated and circ_0001173 downregulated. Circ_0008285 was correlated with total cholesterol and LDL-C levels, while circ_0001173 was associated with glycated hemoglobin.
BackgroundCircular 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).MethodsHigh-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.ResultsIn 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.Conclusionscirc_0008285 plays an important role and provides a clue for the usage of therapeutic targets in the development of GDM.

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