Elias Marjanu Hikmah, Lazim Nurunnajah, Sutaji Zulazmi, Abu Mohammad Azrai, Abdul Karim Abdul Kadir, Ugusman Azizah, Syafruddin Saiful Effendi, Mokhtar Mohd Helmy, Ahmad Mohd Faizal
Advanced Reproductive Centre (ARC) HCTM UKM, Department of Obstetrics & Gynecology, Faculty of Medicine, National University of Malaysia, Jalan Yaacob Latiff, Bandar Tun Razak, Kuala Lumpur 56000, Malaysia.
Faculty of Medicine & Health Sciences, Universiti Sains Islam Malaysia, Nilai 71800, Negeri Sembilan, Malaysia.
Biology (Basel). 2023 Mar 20;12(3):474. doi: 10.3390/biology12030474.
Endometriosis is an inflammatory chronic systemic disease resulting in pelvic pain and infertility. However, despite a high prevalence of endometriosis, disease identification is still insufficient, and a high percentage of misdiagnosing was observed. Hence, a comprehensive study needs to be done to improve our understanding of the pathogenesis of endometriosis. Aberrant hypermethylation of HOXA10 has been reported to play a role in endometriosis. Thus, a comprehensive literature search was conducted to identify the DNA methylation level of HOXA10 among endometriosis patients across populations. The literature search was done using PubMed, Scopus, EBSCOhost, and Science Direct applying (HOXA10 OR "homeobox A10" OR "HOXA-10" OR HOX1) AND ("DNA methylation" OR methylation) AND (endometriosis OR endometrioma) as keywords. From 491 retrieved studies, five original articles investigating the DNA methylation level of HOXA10 from endometrium tissues among endometriosis women were included. All five included studies were classified as high-quality studies. High HOXA10 DNA methylation level was observed in the endometrium tissue of women with endometriosis in all the included studies. The secretory phase was identified as the best sampling time for HOXA10 DNA methylation study in endometriosis, and the most studied DNA methylation site is the promoter region of the HOXA10. However, more studies are needed to expose the HOXA10 mechanism in the pathogenesis of endometriosis.
子宫内膜异位症是一种导致盆腔疼痛和不孕的炎症性慢性全身性疾病。然而,尽管子宫内膜异位症的患病率很高,但疾病诊断仍然不足,误诊率也很高。因此,需要进行全面的研究以增进我们对子宫内膜异位症发病机制的理解。据报道,HOXA10的异常高甲基化在子宫内膜异位症中起作用。因此,我们进行了全面的文献检索,以确定不同人群中子宫内膜异位症患者HOXA10的DNA甲基化水平。文献检索使用PubMed、Scopus、EBSCOhost和Science Direct进行,关键词为(HOXA10或“homeobox A10”或“HOXA - 10”或HOX1)与(“DNA甲基化”或甲基化)与(子宫内膜异位症或子宫内膜瘤)。从检索到的491项研究中,纳入了5篇调查子宫内膜异位症女性子宫内膜组织中HOXA10 DNA甲基化水平的原始文章。所有5项纳入研究均被归类为高质量研究。在所有纳入研究中,子宫内膜异位症女性的子宫内膜组织中均观察到HOXA10 DNA甲基化水平较高。分泌期被确定为子宫内膜异位症中HOXA10 DNA甲基化研究的最佳采样时间,研究最多的DNA甲基化位点是HOXA10的启动子区域。然而,需要更多的研究来揭示HOXA10在子宫内膜异位症发病机制中的作用机制。