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少精子症患者精液中USP7和SET9的表达:一项病例对照研究。

USP7 and SET9 Expression in The Oligospermic Human Semen: A Case-Control Study.

作者信息

Farahani Maryam, Yaghobi Zahra, Ramezani Mina, Piravar Zeynab

机构信息

Department of Biology, Central Tehran Branch, Islamic Azad University, Tehran, Iran.

出版信息

Int J Fertil Steril. 2022 Oct 1;16(4):306-309. doi: 10.22074/ijfs.2021.537310.1174.

Abstract

BACKGROUND

Oligospermia is defined as a less than 15 million per milliliter sperm in each ejaculation of semen. Proper and complete spermatogenesis requires the expression of a large number of genes. As a result, stopping the expression of any of them may lead to disrupt the process of spermatogenesis. In order to understand the disorders of spermatogenesis, it is necessary to study expression of effective genes in the spermatogenesis process. Therefore, in the present study, and gene expression was examined in the healthy and oligospermic men.

MATERIALS AND METHODS

In this case-control study, semen samples of individuals with normal sperm and oligospermia were collected from men who referred to the Roya Clinic (Qom, Iran) according to World Health Organization (WHO) parameters after obtaining consent. Then the expression of and genes in two groups was analyzed using quantitative polymerase chain reaction (qPCR).

RESULTS

There was no difference forage between the healthy and oligospermic individuals (P=0.889). The data showed that, gene expression in the patients was 3.99 times higher than the control group (P<0.001). The expression of gene in the patient was 1.28 times less than the control group, which was not significant (P=0.231). The results indicated that gene expression was increased in the 84% of oligospermic individuals.

CONCLUSION

The gene can be considered as one of the molecular markers in the development of oligospermia.

摘要

背景

少精子症的定义为每次射精精液中精子数量少于每毫升1500万个。正常且完整的精子发生需要大量基因的表达。因此,抑制其中任何一个基因的表达都可能导致精子发生过程受到干扰。为了了解精子发生的紊乱情况,有必要研究精子发生过程中有效基因的表达。因此,在本研究中,对健康男性和少精子症男性的[基因名称1]和[基因名称2]基因表达进行了检测。

材料与方法

在这项病例对照研究中,根据世界卫生组织(WHO)的参数,在获得同意后,从转诊至罗亚诊所(伊朗库姆)的男性中收集了精子正常和少精子症个体的精液样本。然后使用定量聚合酶链反应(qPCR)分析两组中[基因名称1]和[基因名称2]基因的表达。

结果

健康个体和少精子症个体之间的年龄没有差异(P = 0.889)。数据显示,患者组中[基因名称1]基因的表达比对照组高3.99倍(P < 0.001)。患者组中[基因名称2]基因的表达比对照组低1.28倍,但差异不显著(P = 0.231)。结果表明,84%的少精子症个体中[基因名称1]基因表达增加。

结论

[基因名称1]基因可被视为少精子症发生发展中的分子标志物之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b654/9627007/a79bbda4b7df/Int-J-Fertil-Steril-16-306-g01.jpg

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