MicroRNA-141 and MicroRNA-200c Are Overexpressed in Granulosa Cells of Polycystic Ovary Syndrome Patients

被引:15
作者
He, Tingting [1 ,2 ]
Liu, Yuan [3 ]
Jia, Yueyue [4 ]
Wang, Haiyan [5 ]
Yang, Xiao [1 ,2 ]
Lu, Gang [6 ]
Liu, Hongbin [1 ,2 ,6 ]
Shi, Yuhua [1 ,2 ]
机构
[1] Shandong Univ, Ctr Reprod Med, Natl Res Ctr Assisted Reprod Technol & Reprod Gen, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Key Lab Reprod Endocrinol, Minist Educ, Shandong Prov Clin Med Res Ctr Reprod Hlth, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Qilu Hosp, Dept Obstet & Gynecol, Jinan, Shandong, Peoples R China
[4] Liaocheng Peoples Hosp, Liaocheng, Peoples R China
[5] Shandong Univ, Shandong Med Imaging Res Inst, Jinan, Shandong, Peoples R China
[6] Chinese Univ Hong Kong, CUHK SDU Joint Lab Reprod Genet, Sch Biomed Sci, Hong Kong, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
polycystic ovary syndrome; miR-200c; miR-141; granulosa cells; pregnancy complications; FROZEN EMBRYOS; ADIPOSE-TISSUE; EXPRESSION; WOMEN; PROLIFERATION; ASSOCIATION; FRESH;
D O I
10.3389/fmed.2018.00299
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders in reproductive-aged women, affecting 6-8% of women and characterized by hyperandrogenism, ovulatory dysfunction, and polycystic ovarian morphology. Accumulating evidence demonstrates that different microRNAs (miRNAs) expressions may contribute to the pathogenesis of PCOS. Therefore, the goal of this study is to compare the expression levels of miR-141 and miR-200c in granulosa cells isolated from PCOS patients and also evaluate their predictive values for pregnancy complications. First, RNA extraction, reverse transcription, and reverse transcription-polymerase chain reaction (RT-PCR) were performed to assess the expression levels of miR-141 and miR-200c in granulosa cells isolated from 62 PCOS patients and 61 controls. Second, according to each mean of miR-141 and miR-200c measured values in all patients, PCOS, and controls were divided into low-expression group and high-expression group to better evaluate their predictive values for pregnancy complications. Significantly elevated expressions of miR-141 and miR-200c were observed in PCOS patients compared with the controls (p < 0.001 and p = 0.002, respectively). Furthermore, PCOS patients had a significantly increased incidence of pregnancy complications in low-expression groups of miR-141 and miR-200c (p = 0.007 and p = 0.002, respectively). Our findings demonstrated that the expressions of both miR-141 and miR-200c were significantly increased in PCOS patients, which might contribute to the pathogenesis of PCOS. PCOS patients had an increased risk of pregnancy complications in low-expression groups of both miR-141 and miR-200c.
引用
收藏
页数:5
相关论文
共 37 条
  • [11] Risk of maternal mortality in women with severe anaemia during pregnancy and post partum: a multilevel analysis
    Daru, Jahnavi
    Zamora, Javier
    Fernandez-Felix, Borja M.
    Vogel, Joshua
    Oladapo, Olufemi T.
    Morisaki, Naho
    Tuncalp, Oezge
    Torloni, Maria Regina
    Mittal, Suneeta
    Jayaratne, Kapila
    Lumbiganon, Pisake
    Togoobaatar, Ganchimeg
    Thangaratinam, Shakila
    Khan, Khalid S.
    [J]. LANCET GLOBAL HEALTH, 2018, 6 (05): : E548 - E554
  • [12] MicroRNAs as regulators of metabolic disease: pathophysiologic significance and emerging role as biomarkers and therapeutics
    Deiuliis, J. A.
    [J]. INTERNATIONAL JOURNAL OF OBESITY, 2016, 40 (01) : 88 - 101
  • [13] Family-based analysis of INSR polymorphisms in Chinese PCOS
    Du, Jing
    Wang, Jianfeng
    Sun, Xuedong
    Xu, Xinghua
    Zhang, Feng
    Wang, Bin
    Shi, Yuhua
    Chen, Zi-jiang
    [J]. REPRODUCTIVE BIOMEDICINE ONLINE, 2014, 29 (02) : 239 - 244
  • [14] Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS)
    Fauser, BCJM
    Chang, J
    Azziz, R
    Legro, R
    Dewailly, D
    Franks, S
    Tarlatzis, BC
    Fauser, B
    Balen, A
    Bouchard, P
    Dahlgren, E
    Devoto, L
    Diamanti, E
    Dunaif, A
    Filicori, M
    Homburg, R
    Ibanez, L
    Laven, J
    Magoffin, D
    Nestler, J
    Norman, RJ
    Pasquali, R
    Pugeat, M
    Strauss, J
    Tan, S
    Taylor, A
    Wild, R
    Wild, S
    Ehrmann, D
    Lobo, R
    [J]. HUMAN REPRODUCTION, 2004, 19 (01) : 41 - 47
  • [15] Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
    Goodarzi, Mark O.
    Dumesic, Daniel A.
    Chazenbalk, Gregorio
    Azziz, Ricardo
    [J]. NATURE REVIEWS ENDOCRINOLOGY, 2011, 7 (04) : 219 - 231
  • [16] An overview of microRNAs
    Hammond, Scott M.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2015, 87 : 3 - 14
  • [17] Inhibition of SOX17 by MicroRNA 141 and Methylation Activates the WNT Signaling Pathway in Esophageal Cancer
    Jia, Yan
    Yang, Yunsheng
    Zhan, Qimin
    Brock, Malcolm V.
    Zheng, Xiaofei
    Yu, Yuanzi
    Herman, James G.
    Guo, Mingzhou
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2012, 14 (06) : 577 - 585
  • [18] MicroRNA-93 Promotes Ovarian Granulosa Cells Proliferation Through Targeting CDKN1A in Polycystic Ovarian Syndrome
    Jiang, Linlin
    Huang, Jia
    Li, Lin
    Chen, Yaxiao
    Chen, Xiaoli
    Zhao, Xiaomiao
    Yang, Dongzi
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2015, 100 (05) : E729 - E738
  • [19] Differential Gene Expression in Granulosa Cells from Polycystic Ovary Syndrome Patients with and without Insulin Resistance: Identification of Susceptibility Gene Sets through Network Analysis
    Kaur, Surleen
    Archer, Kellie J.
    Devi, M. Gouri
    Kriplani, Alka
    Strauss, Jerome F., III
    Singh, Rita
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (10) : E2016 - E2021
  • [20] MicroRNA-141-3p targets DAPK1 and inhibits apoptosis in rat ovarian granulosa cells
    Li, Dandan
    Xu, Duo
    Xu, Ying
    Chen, Lu
    Li, Chunjin
    Dai, Xiaowei
    Zhang, Lili
    Zheng, Lianwen
    [J]. CELL BIOCHEMISTRY AND FUNCTION, 2017, 35 (04) : 197 - 201