Microarray gene expression analysis of uterosacral ligaments in uterine prolapse

被引:5
作者
Ak, Handan [1 ]
Zeybek, Burak [2 ]
Atay, Sevcan [1 ]
Askar, Niyazi [2 ]
Akdemir, Ali [2 ]
Aydin, Hikmet Hakan [1 ]
机构
[1] Ege Univ, Sch Med, Dept Med Biochem, TR-35100 Izmir, Turkey
[2] Ege Univ, Sch Med, Dept Obstet & Gynecol, Izmir, Turkey
关键词
Uterine prolapse; Uterosacral ligament; Microarray; Gene expression; PELVIC ORGAN PROLAPSE; GENITAL PROLAPSE; HOMEOBOX GENES; RISK-FACTORS; WOMEN; SPLEEN; PREVALENCE; DEFECTS; NKX2.3; FLOOR;
D O I
10.1016/j.clinbiochem.2016.08.004
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Pelvic organ prolapse (POP) is a major health problem that impairs the quality of life with a wide clinical spectrum. Since the uterosacral ligaments provide primary support for the uterus and the upper vagina, we hypothesize that the disruption of these ligaments may lead to a loss of support and eventually contribute to POP. Design and methods: In this study, we therefore investigated whether there are any differences in the transcription profile of uterosacral ligaments in patients with POP when compared to those of the control samples. Seventeen women with POP and 8 non-POP controls undergoing hysterectomy for benign conditions were included in the study. Affymetrix (R) Gene Chip microarrays (Human Hu 133 plus 2.0) were used for whole genome gene expression profiling analysis. Results: There was 1 significantly down-regulated gene, NKX2-3 in patients with POP compared to the controls (p = 4.28464e-013). KIF11 gene was found to be significantly down-regulated in patients with >= 3 deliveries compared to patients with < 3 deliveries (p = 0.0156237). UGT1A1 (p = 2.43388e-005), SCARB1 (p = 1.19001e-006) and NKX2-3 (p = 2.17966e-013) genes were found to be significantly down-regulated in the premenopausal patients compared to the premenopausal controls. UGT1A1 gene was also found to be significantly down-regulated in the post menopausal patients compared to the postmenopausal controls (p = 0.0005). Conclusion: This study provides evidence for a significant down-regulation of the genes that take role in cell cycle, proliferation and embryonic development along with cell adhesion process on the development of POP for the first time. (C) 2016 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1238 / 1242
页数:5
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