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http://purl.uniprot.org/citations/30058675http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30058675http://www.w3.org/2000/01/rdf-schema#comment"

Objective

To detect the expressions of micro ribonucleic acid (miR)-129 and its target gene in uterine fibroid tissues and to investigate the role of miR-129 in the occurrence of uterine fibroid.

Patients and methods

The expressions of miR-129 and its target gene ten-eleven translocation 1 (TET1) were detected via quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Dual-luciferase reporter gene and Western blotting were used to verify the regulatory relation between miR-129 and target gene. The effects of miR-129 on the proliferation, apoptosis, cycle and extracellular matrix (ECM) of uterine fibroid cells were investigated via transfection with miR-129 mimics and TET1 small-interfering RNA (siRNA).

Results

MiR-129 was lowly expressed in uterine fibroid. The expression of miR-129 was regulated by sex hormones. The highly expressed miR-129 promoted apoptosis and inhibited proliferation through reducing the low expression of TET1. At the same time, miR-129 affected the accumulation of ECM.

Conclusions

The expression of miR-129 in uterine fibroid is lower, and the proliferation capacity of tumor cells is enhanced, thus promoting the occurrence and development of uterine fibroid."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.org/dc/terms/identifier"doi:10.26355/eurrev_201807_15492"xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/author"Lin L."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/author"Zhao L."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/author"Han S.C."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/author"Liu H.X."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/author"Yue C."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/author"Lu J.L."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/author"Bi J.L."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/name"Eur Rev Med Pharmacol Sci"xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/pages"4419-4426"xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/title"MiR-129 is involved in the occurrence of uterine fibroid through inhibiting TET1."xsd:string
http://purl.uniprot.org/citations/30058675http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/30058675http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/30058675
http://purl.uniprot.org/citations/30058675http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/30058675
http://purl.uniprot.org/uniprot/#_B3W6H5-mappedCitation-30058675http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30058675
http://purl.uniprot.org/uniprot/#_B3W6H6-mappedCitation-30058675http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30058675
http://purl.uniprot.org/uniprot/#_B3W6H8-mappedCitation-30058675http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30058675
http://purl.uniprot.org/uniprot/#_Q8NFU7-mappedCitation-30058675http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30058675
http://purl.uniprot.org/uniprot/Q8NFU7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30058675
http://purl.uniprot.org/uniprot/B3W6H5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30058675
http://purl.uniprot.org/uniprot/B3W6H8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30058675
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