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长链非编码RNA作为人乳头瘤病毒16型促进头颈部鳞状细胞癌髓源性抑制细胞招募过程中的一种中间介质。

LncRNAs as an intermediate in HPV16 promoting myeloid-derived suppressor cell recruitment of head and neck squamous cell carcinoma.

作者信息

Ma Xiangrui, Sheng Surui, Wu Jingbiao, Jiang Yaping, Gao Xiaolei, Cen Xiao, Wu Jiashun, Wang Shasha, Tang Yajie, Tang Yaling, Liang Xinhua

机构信息

State Key Laboratory of Oral Diseases, West China Hospital of Stomatology (Sichuan University), Chengdu, Sichuan 610041, China.

Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Binzhou Medical College, Binzhou, Shandong 256600, China.

出版信息

Oncotarget. 2017 Jun 27;8(26):42061-42075. doi: 10.18632/oncotarget.14939.

Abstract

The emerging evidence showed that long noncoding RNAs (lncRNAs) are involved in cell growth and apoptosis as well as cancer progression and metastasis of malignant tumor, however, limited data are available on the role of lncRNAs in human papillomavirus (HPV)-associated Head and neck squamous cell carcinomas (HNSCC). Here, we demonstrated that 23.98% of 196 HNSCC cases in Southwest China could be classified as HPV16 infection. The number of MDSCs in HPV-positive HNSCC was significantly higher than normal control, indicating that HPV infection may promote MDSCs aggregation. Then, we applied an array-based approach to monitor the lncRNA expression between HPV-positive HNSCC, HPV-negative HNSCC and normal oral mucous, and obtained 132 different lncRNAs in different HPV infected states of HNSCC. HOTAIR, PROM1, CCAT1, and MUC19 mRNA levels, determined by qRT-PCR were inversely correlated with MDSCs collection of HPV-associated HNSCC in 2 independent patient cohorts. The results may provide a rationale for the further evaluation of lncRNAs as a molecular target to elucidate the molecular mechanism of HPV promoting MDSCs collection of HNSCC.

摘要

新出现的证据表明,长链非编码RNA(lncRNAs)参与细胞生长、凋亡以及恶性肿瘤的癌症进展和转移,然而,关于lncRNAs在人乳头瘤病毒(HPV)相关的头颈部鳞状细胞癌(HNSCC)中的作用,现有数据有限。在此,我们证明中国西南部196例HNSCC病例中有23.98%可归类为HPV16感染。HPV阳性HNSCC中髓源性抑制细胞(MDSCs)的数量显著高于正常对照,表明HPV感染可能促进MDSCs聚集。然后,我们采用基于芯片的方法监测HPV阳性HNSCC、HPV阴性HNSCC和正常口腔黏膜之间的lncRNA表达,并在HNSCC不同的HPV感染状态下获得了132种不同的lncRNAs。通过qRT-PCR测定的HOTAIR、PROM1、CCAT1和MUC19 mRNA水平与2个独立患者队列中HPV相关HNSCC的MDSCs收集呈负相关。这些结果可能为进一步评估lncRNAs作为分子靶点以阐明HPV促进HNSCC的MDSCs收集的分子机制提供理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4e6/5522049/8e2584f7e33e/oncotarget-08-42061-g001.jpg

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