Integrated Analysis of Gene Expression Profiles of T-lymphocytes in human T cell leukemia virus type 1 (HTLV-1) associated disease: A bioinformatics analysis

Integrated Analysis of Gene Expression Profiles of T-lymphocytes in human T cell leukemia virus type 1 (HTLV-1) associated disease: A bioinformatics analysis


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نویسندگان: امین عبادی , امید قلیزاده , وحدت پورطهماسبی

عنوان کنگره / همایش: کنفرانس بین المللی ژنتیک و ژنومیک انسانی , Iran (Islamic Republic) , یزد ,

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دانشکده/مرکز مربوطه بیماری های عفونی و گرمسیری
کد مقاله 77539
عنوان فارسی مقاله Integrated Analysis of Gene Expression Profiles of T-lymphocytes in human T cell leukemia virus type 1 (HTLV-1) associated disease: A bioinformatics analysis
عنوان لاتین مقاله Integrated Analysis of Gene Expression Profiles of T-lymphocytes in human T cell leukemia virus type 1 (HTLV-1) associated disease: A bioinformatics analysis
نوع ارائه پوستر
عنوان کنگره / همایش کنفرانس بین المللی ژنتیک و ژنومیک انسانی
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش Iran (Islamic Republic)
شهر محل برگزاری کنگره/ همایش یزد
سال انتشار/ ارائه شمسی 1400
سال انتشار/ارائه میلادی
تاریخ شمسی شروع و خاتمه کنگره/همایش 1400/09/10 الی 1400/09/11
آدرس لینک مقاله/ همایش در شبکه اینترنت https://yazdgenetics.ir/upload/Single/Files/Poster_33720.pdf?t=637743260860019131&t=637743260860019131
آدرس علمی (Affiliation) نویسنده متقاضی Infectious and Tropical Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

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نویسنده نفر چندم مقاله
امین عبادیاول
امید قلیزادهسوم
وحدت پورطهماسبیچهارم

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عنوان متن
خلاصه مقالهBackground: Human T-lymphotropic virus type 1 (HTLV-1) is the cause of adult T-cell leukemia-lymphomas (ATL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). The goal of present study was to investigating the gene expression analysis of gene expression pattern for ATL HAM/TSP. Materials and methods: Microarray gene expression profiling of T lymphocytes from HTLV-1 associated disease and healthy control were obtained from Gene Expression. Bioinformatics tools (GEO accession: GSE19080) were performed to identify differentially expressed genes (DEGs). Among the generated DEGs, we constructed protein-protein interaction (PPI) of HAM/TSM and ATL in comparison to asymptomatic carriers (ACs). Subsequently, gene ontology and PPI analysis were performed. Topological properties of each PPI were measured using Network-Analyzer, a network analysis plug-in of Cytoscape, to identify the most important functional hub genes within the networks. Results: We found that the majority of DEGs in ATL and HAM/TSP were importantly implicated in immune response categories. The nodes and edges number of normal-AC, AC-ATL and ATLHAM/TSP PPIs were 168 and 145, 116 and 97, and 275 and 327, respectively. Based on the topological analysis of protein-protein interaction networks, APP (Amyloid Beta Precursor Protein) was detected as the critical player of HTLV-1 disease progression. The expression of APP had a significant negative correlation in ATL (down-regulated) and HAM/TSP (up-regulated) samples. PTK2, PIK3R1, COPS5, CALM1 and HLA-B associated with disease progression. Conclusion: Dysregulation of immune response associated transcripts play a critical role in HTLV-1 disease progression. Immune response associated genes may be biomarker for prognosis in cancer development and therapeutic targets.
کلمات کلیدیHTLV-1, ATL, HTLV-1-associated myelopathy/tropical spastic paraparesis, Gene expression

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