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