4.5 Article

Screening differential circular RNAs expression profiles in Vulvar Lichen Sclerosus

Journal

BIOMEDICAL ENGINEERING ONLINE
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12938-022-01013-7

Keywords

Vulvar lichen sclerosus; circRNAs; mRNAs; lncRNAs

Funding

  1. Natural Science Foundation of Beijing Municipality [7172192]

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This study analyzed the expression profile of circRNAs in vulvar lichen sclerosus and identified their potential association with the pathogenesis and pathological process of the disease.
Background Vulvar lichen sclerosus (VLS) is one of the most common clinical manifestations of vulva. Thirteen percent of women have symptomatic vulvar diseases. The aim of this study is to investigate the expression profile of circular RNA (circRNAs) in vulvar lichen sclerosus, and to identify the underlying core genes of VLS. Methods We removed rRNA for sequencing, and screened the differentially expressed messenger RNA (mRNAs), long non-coding RNA (lncRNAs) and single-stranded circRNA in 20 groups of VLS tissues and 20 groups of healthy female vulvar skin tissues. Bioinformatics analysis was used to analyze its potential functions. Results A total of 2545 differentially expressed mRNAs were assessed in VLS patients, of which 1541 samples were up-regulated and 1004 samples were down-regulated. A total of 1453 differentially expressed lncRNAs were assessed, of which 812 samples were up-regulated and 641 samples were down-regulated. A total of 79 differentially expressed circRNAs were assessed, of which 54 were up-regulated and 25 were down-regulated. The differential expression of circRNAs was closely related to biological processes and molecular functions. The differences in circRNAs were mainly related to the human T-cell leukemia virus 1 infection signaling pathway and the axon guidance signaling pathway. Conclusion The profile of abnormal regulation of circRNA exists in VLS. According to biological informatics analysis, the dysregulation of circRNAs may be related to the pathogenesis and pathological process of VLS.

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