详细信息
High throughput microRNAs sequencing profile of serum exosomes in women with and without polycystic ovarian syndrome ( SCI-EXPANDED收录) 被引量:15
文献类型:期刊文献
英文题名:High throughput microRNAs sequencing profile of serum exosomes in women with and without polycystic ovarian syndrome
作者:Zhang, Feng[1,2];Li, Su-Ping[3];Zhang, Tao[1,2];Yu, Bin[1,2];Zhang, Juan[1,2];Ding, Hai-Gang[1,2];Ye, Fei-Jun[4];Yuan, Hua[1,2];Ma, Ying-Ying[1,2];Pan, Hai-Tao[1,2];He, Yao[1,2]
机构:[1]Shaoxing Matern & Child Hlth Care Hosp, Shaoxing, Peoples R China;[2]Shaoxing Univ, Obstet & Gynecol Hosp, Shaoxing, Peoples R China;[3]Jiaxing Univ, Women & Childrens Hosp, Jiaxing, Peoples R China;[4]Zhoushan Matern & Child Hlth Care Hosp, Zhoushan, Peoples R China
年份:2021
卷号:9
外文期刊名:PEERJ
收录:SCI-EXPANDED(收录号:WOS:000628808100005)、、Scopus(收录号:2-s2.0-85102441699)、WOS
基金:This work was supported by the National Natural Science Foundation of China (81701522 and 82071729), the Zhejiang Provincial Natural Science Foundation of China (LY19H040002), the Science Technology Department of Zhejiang Province, China (LGF21H040003, LGF21H040004, LGF19H040004, LGD20H040001, LGF18H180015) and the Health Commission of Zhejiang Province, China (2021KY375, 2021KY1154, 2021KY1157, 2020KY1001, 2018KY844, 2018KY845, 2018KY848, 2019KY229, 2019KY230, 2019RC296, 2019KY717); the Science Technology Department of Shaoxing, China (2020A13032, 2020A13034, 2020A13035, 2020A13037, 2018C30039, 2018C30042, 2018C30043, 2018C30044, 2018C30048). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
语种:英文
外文关键词:PCOS; Serum; Exosomes; microRNAs; Biomarker
外文摘要:Background. Polycystic ovary syndrome (PCOS) is the most common type of endocrine disorder, affecting 5-11% of women of reproductive age worldwide. microRNAs (miRNAs) stably exist in circulating blood encapsulated in extracellular vesicles such as exosomes; therefore, serum miRNAs have the potential to serve as novel PCOS biomarkers. Methods. To identify miRNA biomarkers that are associated with PCOS, we performed a comprehensive sequence-based characterization of the PCOS serum miRNA landscape. The serum exosomes were successfully isolated and characterized in a variety of ways. Next, sequence-based analysis was performed on serum exosomes to screen the differentially expressed miRNAs in women with and without PCOS. Results. The sequence data revealed that the levels of 54 miRNAs significantly differed between PCOS patients and normal controls. The levels of these miRNAs were detected by RT-qPCR. The results show that hsa-miR-1299, hsa-miR-6818-5p hsa-miR-1925p, and hsa-miR-145-5p are significantly differentially expressed in PCOS patients serum exosomes and identify these microRNAs as potential biomarkers for PCOS. Furthermore, Gene Ontology (GO) analyses and KEGG pathway analyses of the miRNA targets further allowed to explore the potential implication of the miRNAs in PCOS. Conclusion. Our findings suggest that serum exosomal miRNAs serve important roles in PCOS and may be used as novel molecular biomarkers for clinical diagnosis.
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