Safa Alshattawi , Rand Moushtaq Taleb , Ghanyia Jasim shanyoor , Mohanad K. Aneed Al-Saedi , Maryam Qasim Mohammed
{"title":"将炎症与基因表达联系起来:来自强直性脊柱炎的GPR65、NUAK2和OPG的见解","authors":"Safa Alshattawi , Rand Moushtaq Taleb , Ghanyia Jasim shanyoor , Mohanad K. Aneed Al-Saedi , Maryam Qasim Mohammed","doi":"10.1016/j.genrep.2025.102315","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Ankylosing spondylitis (AS) is a chronic inflammatory disease that primarily affects the spine, leading to joint inflammation. Gene expression plays a pivotal role in the pathogenesis of AS, and understanding its underlying genetic mechanisms may enhance both diagnostic accuracy and therapeutic strategies. This study aimed to evaluate the gene expression levels of <em>GPR65</em> and <em>NUAK2</em>, along with the protein level of Osteoprotegerin (OPG), in Iraqi individuals diagnosed with AS.</div></div><div><h3>Methods</h3><div>A case-control study was conducted, involving 50 patients with AS and 50 healthy controls. Blood samples were collected to assess the erythrocyte sedimentation rate (ESR), while serum levels of C-reactive protein (CRP) and OPG were measured using ELISA. Total RNA was extracted using a specialized kit, followed by cDNA synthesis and quantitative real-time PCR (qRT-PCR) to analyze the expression levels of GPR65 and NUAK2.</div></div><div><h3>Results</h3><div>The findings revealed a significant increase in OPG levels (p < 0.001**) and <em>GPR65</em> expression (p < 0.001**), alongside a downregulation of <em>NUAK2</em> expression (p = 0.05*) in AS patients compared to healthy controls.</div></div><div><h3>Conclusions</h3><div>These results suggest that elevated OPG levels and increased <em>GPR65</em> expression may contribute to the inflammatory processes in AS, whereas reduced <em>NUAK2</em> expression might impair the regulation of inflammation. Furthermore, OPG, <em>GPR65</em>, and <em>NUAK2</em> exhibited strong diagnostic potential, with high specificity and sensitivity demonstrated through ROC analysis. The OPG and <em>GPR65</em> may enhance the diagnosis and monitoring of AS and underscore the need for further research into their roles in disease progression and as potential targets for therapy.</div></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"41 ","pages":"Article 102315"},"PeriodicalIF":0.9000,"publicationDate":"2025-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Linking inflammation to gene expression: Insights from GPR65, NUAK2, and OPG in ankylosing spondylitis\",\"authors\":\"Safa Alshattawi , Rand Moushtaq Taleb , Ghanyia Jasim shanyoor , Mohanad K. Aneed Al-Saedi , Maryam Qasim Mohammed\",\"doi\":\"10.1016/j.genrep.2025.102315\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Ankylosing spondylitis (AS) is a chronic inflammatory disease that primarily affects the spine, leading to joint inflammation. Gene expression plays a pivotal role in the pathogenesis of AS, and understanding its underlying genetic mechanisms may enhance both diagnostic accuracy and therapeutic strategies. This study aimed to evaluate the gene expression levels of <em>GPR65</em> and <em>NUAK2</em>, along with the protein level of Osteoprotegerin (OPG), in Iraqi individuals diagnosed with AS.</div></div><div><h3>Methods</h3><div>A case-control study was conducted, involving 50 patients with AS and 50 healthy controls. Blood samples were collected to assess the erythrocyte sedimentation rate (ESR), while serum levels of C-reactive protein (CRP) and OPG were measured using ELISA. Total RNA was extracted using a specialized kit, followed by cDNA synthesis and quantitative real-time PCR (qRT-PCR) to analyze the expression levels of GPR65 and NUAK2.</div></div><div><h3>Results</h3><div>The findings revealed a significant increase in OPG levels (p < 0.001**) and <em>GPR65</em> expression (p < 0.001**), alongside a downregulation of <em>NUAK2</em> expression (p = 0.05*) in AS patients compared to healthy controls.</div></div><div><h3>Conclusions</h3><div>These results suggest that elevated OPG levels and increased <em>GPR65</em> expression may contribute to the inflammatory processes in AS, whereas reduced <em>NUAK2</em> expression might impair the regulation of inflammation. Furthermore, OPG, <em>GPR65</em>, and <em>NUAK2</em> exhibited strong diagnostic potential, with high specificity and sensitivity demonstrated through ROC analysis. The OPG and <em>GPR65</em> may enhance the diagnosis and monitoring of AS and underscore the need for further research into their roles in disease progression and as potential targets for therapy.</div></div>\",\"PeriodicalId\":12673,\"journal\":{\"name\":\"Gene Reports\",\"volume\":\"41 \",\"pages\":\"Article 102315\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-08-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Gene Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2452014425001888\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452014425001888","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Linking inflammation to gene expression: Insights from GPR65, NUAK2, and OPG in ankylosing spondylitis
Background
Ankylosing spondylitis (AS) is a chronic inflammatory disease that primarily affects the spine, leading to joint inflammation. Gene expression plays a pivotal role in the pathogenesis of AS, and understanding its underlying genetic mechanisms may enhance both diagnostic accuracy and therapeutic strategies. This study aimed to evaluate the gene expression levels of GPR65 and NUAK2, along with the protein level of Osteoprotegerin (OPG), in Iraqi individuals diagnosed with AS.
Methods
A case-control study was conducted, involving 50 patients with AS and 50 healthy controls. Blood samples were collected to assess the erythrocyte sedimentation rate (ESR), while serum levels of C-reactive protein (CRP) and OPG were measured using ELISA. Total RNA was extracted using a specialized kit, followed by cDNA synthesis and quantitative real-time PCR (qRT-PCR) to analyze the expression levels of GPR65 and NUAK2.
Results
The findings revealed a significant increase in OPG levels (p < 0.001**) and GPR65 expression (p < 0.001**), alongside a downregulation of NUAK2 expression (p = 0.05*) in AS patients compared to healthy controls.
Conclusions
These results suggest that elevated OPG levels and increased GPR65 expression may contribute to the inflammatory processes in AS, whereas reduced NUAK2 expression might impair the regulation of inflammation. Furthermore, OPG, GPR65, and NUAK2 exhibited strong diagnostic potential, with high specificity and sensitivity demonstrated through ROC analysis. The OPG and GPR65 may enhance the diagnosis and monitoring of AS and underscore the need for further research into their roles in disease progression and as potential targets for therapy.
Gene ReportsBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍:
Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.