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HIV 感染中的肺部恶性肿瘤的分子变化。

Molecular Changes of Lung Malignancy in HIV Infection.

机构信息

Shanghai Public Health Clinical Center, Fudan University, 2901 Caolang Road, Jinshan District, Shanghai, 201508, P.R. China.

Department of Laboratory Medicine, Zhoupu Hospital Affiliated to Shanghai University of Medicine & Health Sciences, Shanghai, 201318, China.

出版信息

Sci Rep. 2018 Sep 3;8(1):13128. doi: 10.1038/s41598-018-31572-6.

DOI:10.1038/s41598-018-31572-6
PMID:30177858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6120915/
Abstract

Malignancy of the lung is a major source of morbidity and mortality in persons with human immunodeficiency virus infection; as the most prevalent non-acquired immunodeficiency syndrome-defining malignancy, it represents an important and growing problem confronting HIV-infected patients. To evaluate the molecular changes of lung malignancy in HIV infection, we analyzed differential gene expression profiles and screened for early detection biomarkers of HIV-associated lung cancer using Affymetrix arrays and IPA analysis. A total of 59 patients were diagnosed with HIV-associated lung cancer from Jan 2010 to May 2018. The primary outcome was a significant difference in survival outcome between stages III-IV (10.46 ± 1.87 months) and I-II (17.66 ± 2.88 months). We identified 758 differentially expressed genes in HIV-associated lung cancer. The expression levels of SIX1 and TFAP2A are specifically increased in HIV-associated lung cancer and are associated with poorly differentiated tumor tissue. We also found decreased ADH1B, INMT and SYNPO2 mRNA levels in HIV lung cancer. A comprehensive network and pathway analysis of the dysregulated genes revealed that these genes were associated with four network functions and six canonical pathways relevant to the development of HIV-associated lung cancer. The molecular changes in lung malignancy may help screen the growing population of HIV patients who have or will develop this malignancy.

摘要

肺癌是人类免疫缺陷病毒(HIV)感染者发病和死亡的主要原因之一;作为最常见的非获得性免疫缺陷综合征(AIDS)定义性恶性肿瘤,它是 HIV 感染者面临的一个重要且日益严重的问题。为了评估 HIV 感染相关肺癌的分子变化,我们使用 Affymetrix 微阵列和 IPA 分析,分析了差异基因表达谱,并筛选了 HIV 相关肺癌的早期检测生物标志物。2010 年 1 月至 2018 年 5 月,共诊断出 59 例 HIV 相关肺癌患者。主要结局为 III-IV 期(10.46±1.87 个月)和 I-II 期(17.66±2.88 个月)之间的生存结果差异有统计学意义。我们在 HIV 相关肺癌中发现了 758 个差异表达基因。SIX1 和 TFAP2A 的表达水平在 HIV 相关肺癌中特异性增加,与分化不良的肿瘤组织相关。我们还发现 HIV 肺癌中 ADH1B、INMT 和 SYNPO2 mRNA 水平降低。对失调基因的综合网络和途径分析表明,这些基因与与 HIV 相关肺癌发生发展相关的四个网络功能和六个经典途径有关。肺癌恶性肿瘤的分子变化可能有助于筛选出越来越多的 HIV 患者,这些患者已经或将要患上这种恶性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/5b7a3e5644c2/41598_2018_31572_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/15c7cef21156/41598_2018_31572_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/34ec82bd9b6b/41598_2018_31572_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/4fbbf51144f0/41598_2018_31572_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/5b7a3e5644c2/41598_2018_31572_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/15c7cef21156/41598_2018_31572_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/34ec82bd9b6b/41598_2018_31572_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/4fbbf51144f0/41598_2018_31572_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb4/6120915/5b7a3e5644c2/41598_2018_31572_Fig4_HTML.jpg

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