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绝经前和绝经后盆腔器官脱垂女性阴道中LOXL1的表达

Vaginal Expression of LOXL1 in Premenopausal and Postmenopausal Women With Pelvic Organ Prolapse.

作者信息

Kow Nathan, Ridgeway Beri, Kuang Mei, Butler Robert S, Damaser Margot S

机构信息

From the *Center of Urogynecology and Pelvic Floor Disorders, Obstetrics, Gynecology, and Women's Health Institute, †Department of Biomedical Engineering, Lerner Research Institute, and ‡Department of Quantitative Health Sciences, Cleveland Clinic; §Advanced Platform Technology Center, Louis Stokes Cleveland VA Medical Center; and ∥Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, OH.

出版信息

Female Pelvic Med Reconstr Surg. 2016 Jul-Aug;22(4):229-35. doi: 10.1097/SPV.0000000000000251.

Abstract

OBJECTIVES

This study aimed to compare cellular expression of lysyl oxidase-like 1 (LOXL1), a key enzyme in elastin metabolism, of premenopausal women with pelvic organ prolapse (POP) compared with premenopausal controls without POP and postmenopausal women with POP. In addition, we examined whether variation of LOXL1 expression was dependent on biopsy site.

METHODS

A standardized protocol was utilized to obtain vaginal biopsies from 30 women (10 premenopausal POP, 10 postmenopausal POP, and 10 premenopausal non-POP). Expression levels of messenger RNA (mRNA) and protein of LOXL1 were determined using real-time quantitative polymerase chain reactions and enzyme-linked immunosorbant assays. Analysis was performed to determine if there were differences between group or biopsy site.

RESULTS

Significant differences in LOXL1 mRNA expression were found between patient groups (P = 0.0033). LOXL1 mRNA expression (relative to 18S) was upregulated in the postmenopausal POP group (54.5 ± 14.7) compared with the premenopausal POP group (5.2 ± 14.7, P = 0.0034) and the premenopausal non-POP group (23 ± 18, P = 0.0359). No significant differences in LOXL1 protein expression (nanogram/milliliter per microgram total protein) were seen between groups (premenopausal POP, 3.2 × 10 ± 6.3 × 10; postmenopausal POP, 4.3 × 10 ± 6.3 × 10; premenopausal non-POP, 5.0 × 10 ± 7.7 × 10; P = 0.15). No differences in mRNA expression were seen between sites (P = 0.74), but significant variation was noted in protein expression (P = 0.001).

CONCLUSIONS

Premenopausal and postmenopausal women with POP exhibit differential expression of LOXL1 suggesting different pathways in the pathogenesis of POP. The role of biopsy location on LOXL1 expression requires further investigation.

摘要

目的

本研究旨在比较绝经前盆腔器官脱垂(POP)女性与无POP的绝经前对照以及绝经后POP女性中弹性蛋白代谢关键酶赖氨酰氧化酶样1(LOXL1)的细胞表达。此外,我们还研究了LOXL1表达的变化是否依赖于活检部位。

方法

采用标准化方案从30名女性(10名绝经前POP患者、10名绝经后POP患者和10名绝经前无POP者)获取阴道活检组织。使用实时定量聚合酶链反应和酶联免疫吸附测定法测定LOXL1的信使核糖核酸(mRNA)和蛋白质表达水平。进行分析以确定组间或活检部位之间是否存在差异。

结果

患者组之间LOXL1 mRNA表达存在显著差异(P = 0.0033)。与绝经前POP组(5.2±14.7,P = 0.0034)和绝经前无POP组(23±18,P = 0.0359)相比,绝经后POP组中LOXL1 mRNA表达(相对于18S)上调(54.5±14.7)。组间LOXL1蛋白表达(纳克/毫升/微克总蛋白)未见显著差异(绝经前POP组,3.2×10±6.3×10;绝经后POP组,4.3×10±6.3×10;绝经前无POP组,5.0×10±7.7×10;P = 0.15)。各部位之间mRNA表达未见差异(P = 0.74),但蛋白表达存在显著差异(P = 0.001)。结论:绝经前和绝经后POP女性表现出LOXL1的差异表达,提示POP发病机制中的不同途径。活检部位对LOXL1表达的作用需要进一步研究。

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