人类前列腺癌中男性不育基因的基因组学和转录组学特征研究:一项硅学分析。

IF 2.1 4区 医学 Q3 ANDROLOGY
Farima Said Ali-Samani, Arman Shahrisa, Maryam Tahmasebi-Birgani, Mohammadreza Hajjari, Pegah Ghandil
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引用次数: 0

摘要

世界卫生组织已将不孕症视为国际公共卫生问题。近七分之一的夫妇患有不育症,而男性因素占不育症病例的 50%。男性不育与某些癌症(如睾丸生殖细胞癌、前列腺癌和结肠癌)之间存在着明显的联系。有两种可能性支持这一发现:1)癌症治疗会影响生育因素;2)癌症患者的不育基因发生了改变。虽然之前发表的研究大多集中在第一个因素上,但还没有文章证实遗传因素的作用。在这项硅学研究中,我们收集了大量与不孕症有关的基因(n = 17703)。这些基因来自男性不育症的 NGS 面板测试和全面的文献综述或在线数据库。前列腺腺癌基因组和转录组原始数据从 cBioPortal 癌症数据集下载。其中包括 494 名前列腺癌患者的 494 项突变数据、489 项 CNA 数据和 493 项 RNA seqV2 数据。TCGA RNA-Seq原始数据使用cgdsr扩展包在R语言中提取,阈值为相对于正常样本的±2。观察数据显示,男性不育基因分布在人类基因组中。在本研究分析的 17703 个基因中,包括 OR9Q1、H4C6 和 PSG7 在内的三个基因的基因组图谱在 100% 的患者(n = 493)中发生了改变。大多数患者(>98%)的基因改变与基因表达变化有关。总之,这项研究表明,在前列腺癌患者中,一些男性不育基因的基因组和转录组学模式发生了显著改变,并提示遗传因素在癌症患者不育症的发生中可能扮演了重要角色。我们的信息可作为设计男性不育基因数据库的资料来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of the genomics and transcriptomics profiles of male-infertility genes in human prostate cancer: an in silico analysis.

The World Health Organization has considered the infertility as an international public health problem. Infertility affect nearly 1 in 7 couples and male component contributes to 50% of infertility cases. There is a clear link between male infertility and some cancers such as testicular germ cell, prostate and colon cancers. Two possibilities support this finding: 1) Cancer treatments can affect the fertility factors 2) Genetic profile of infertility genes have been altered in cancer patients. Although the previously published researches have mostly focused on the first factor, no article has yet confirmed the role of genetic factors. In this in silico study, we collected the large number of genes (n = 17703) involved in infertility. These genes were collected from NGS panel tests of male infertility and comprehensive literature review or online data base. The Prostate Adenocarcinoma genomic and transcriptomics raw data were downloaded from the cBioPortal Cancer dataset. This included with 494 patients of Prostate Cancer with 494 mutation data, 489 with CNA and 493 with RNA seqV2 data. TCGA RNA-Seq raw data was extracted in R using the cgdsr extension package with a threshold of ±2 relative to normal samples. The observed data showed that male infertility genes have been distributed through the human genome. Among the 17703 analyzed genes of this study, the genomic profile of three genes including OR9Q1, H4C6 and PSG7 were changed approximately in 100% of (n = 493) patients. In most of patients (>98%), genetic alteration was related to change in gene expression. In conclusion, this study showed that the genomic and transcriptomics patterns of some male-infertility genes are notably altered in patients of prostate cancer and suggested a possible role of genetic factors in occurrence of infertility in cancer patients. Our information can be used as a source for the design of genetic database of male-infertility.

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来源期刊
CiteScore
4.30
自引率
4.20%
发文量
27
审稿时长
>12 weeks
期刊介绍: Systems Biology in Reproductive Medicine, SBiRM, publishes Research Articles, Communications, Applications Notes that include protocols a Clinical Corner that includes case reports, Review Articles and Hypotheses and Letters to the Editor on human and animal reproduction. The journal will highlight the use of systems approaches including genomic, cellular, proteomic, metabolomic, bioinformatic, molecular, and biochemical, to address fundamental questions in reproductive biology, reproductive medicine, and translational research. The journal publishes research involving human and animal gametes, stem cells, developmental biology and toxicology, and clinical care in reproductive medicine. Specific areas of interest to the journal include: male factor infertility and germ cell biology, reproductive technologies (gamete micro-manipulation and cryopreservation, in vitro fertilization/embryo transfer (IVF/ET) and contraception. Research that is directed towards developing new or enhanced technologies for clinical medicine or scientific research in reproduction is of significant interest to the journal.
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