Department of Laboratory Medicine, The Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Department of Immunology, Jiangsu Key Laboratory of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, China.
Front Immunol. 2018 Mar 12;9:473. doi: 10.3389/fimmu.2018.00473. eCollection 2018.
HOXA transcript antisense RNA myeloid-specific 1 (HOTAIRM1) is a long non-coding RNA that has been shown to be a key regulator of myeloid cell development by targeting HOXA1. Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of immature myeloid cells that possess immunosuppressive function. However, the impact of HOTAIRM1 on the development of MDSCs remains unknown. In this study, we demonstrated that HOTAIRM1 was expressed in MDSCs and that overexpression of HOTAIRM1 could downregulate the expression of suppressive molecules in MDSCs. In addition, HOTAIRM1 levels were observed to be decreased in the peripheral blood cells of lung cancer patients compared with those of healthy controls. By analyzing HOTAIRM1 expression levels in different types of lung cancer, we found that HOTAIRM1 was mainly expressed in lung adenocarcinoma. Finally, it was confirmed that HOTAIRM1 could enhance the expression of HOXA1 in MDSCs and that high levels of HOXA1, the target gene of HOTAIRM1, could delay tumor progression and enhance the antitumor immune response by downregulating the immunosuppression of MDSCs. Taken together, this study illustrates that HOTAIRM1/HOXA1 downregulates the immunosuppressive function of MDSCs and may be a potential therapeutic target in lung cancer.
HOXA 转录反义 RNA 髓系特异性 1(HOTAIRM1)是一种长非编码 RNA,通过靶向 HOXA1 被证明是髓系细胞发育的关键调节剂。髓系来源的抑制细胞(MDSCs)是一群具有免疫抑制功能的未成熟髓系细胞。然而,HOTAIRM1 对 MDSC 发育的影响尚不清楚。在这项研究中,我们证明了 HOTAIRM1 在 MDSC 中表达,并且过表达 HOTAIRM1 可以下调 MDSC 中抑制分子的表达。此外,与健康对照组相比,肺癌患者外周血细胞中的 HOTAIRM1 水平降低。通过分析不同类型肺癌中 HOTAIRM1 的表达水平,我们发现 HOTAIRM1 主要在肺腺癌中表达。最后,证实 HOTAIRM1 可以增强 MDSC 中 HOXA1 的表达,而 HOTAIRM1 的靶基因 HOXA1 可以通过下调 MDSC 的免疫抑制作用来延迟肿瘤进展并增强抗肿瘤免疫反应。综上所述,这项研究表明 HOTAIRM1/HOXA1 下调 MDSC 的免疫抑制功能,可能是肺癌的潜在治疗靶点。