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miR-34a-5p通过靶向Flotillin-2在头颈部鳞状细胞癌进展中发挥肿瘤抑制作用。

miR-34a-5p functions as a tumor suppressor in head and neck squamous cell cancer progression by targeting Flotillin-2.

作者信息

Li Xiang, Zhao Shouwei, Fu Yu, Zhang Ping, Zhang Zhenxing, Cheng Jie, Liu Laikui, Jiang Hongbing

机构信息

Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, 136 Hanzhong Road, Nanjing 210029, Jiangsu Province, China.

Jiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 136 Hanzhong Road, Nanjing 210029, Jiangsu Province, China.

出版信息

Int J Biol Sci. 2021 Oct 21;17(15):4327-4339. doi: 10.7150/ijbs.64851. eCollection 2021.

DOI:10.7150/ijbs.64851
PMID:34803501
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8579463/
Abstract

While a number of therapeutic advances have been made in recent years, the overall survival of patients with head and neck squamous cell cancer (HNSCC) remains poor. MicroRNAs (miRNAs) are key drivers of oncogenic progression, with miR-34a-5p downregulation having been observed in many different tumor types. Here, we assessed the link between miR-34a-5p and HNSCC progression and the mechanistic basis for this relationship. Levels of miR-34a-5p in HNSCC tumors and cell lines were assessed via qPCR, after which we explored the functional importance of this miRNA in this oncogenic setting. Through luciferase reporter assays, the ability of miR-34a-5p to regulate flotillin-2 (FLOT-2) was further clarified. Overall, these analyses revealed that HNSCC tumors and cells exhibited marked miR-34a-5p downregulation that was linked to the progression of this tumor type. At a functional level, miR-34a-5p constrained the proliferation, migratory/invasive activity, and epithelial-mesenchymal transition induction in HNSCC cells. At the mechanistic level, miR-34a-5p was found to suppress FLOT-2 expression and to activate the MEK/ERK1/2 pathway. Overall, these results suggest that miR-34a-5p can function as a tumor suppressor miRNA in HNSCC owing to its ability to target FLOT-2, highlighting the promise of targeting this regulatory axis to treat HNSCC.

摘要

尽管近年来在治疗方面取得了一些进展,但头颈部鳞状细胞癌(HNSCC)患者的总体生存率仍然很低。微小RNA(miRNA)是致癌进展的关键驱动因素,在许多不同肿瘤类型中都观察到miR-34a-5p表达下调。在此,我们评估了miR-34a-5p与HNSCC进展之间的联系以及这种关系的机制基础。通过qPCR评估HNSCC肿瘤和细胞系中miR-34a-5p的水平,之后我们探讨了这种miRNA在这种致癌环境中的功能重要性。通过荧光素酶报告基因检测,进一步阐明了miR-34a-5p调节 flotillin-2(FLOT-2)的能力。总体而言,这些分析表明,HNSCC肿瘤和细胞表现出明显的miR-34a-5p下调,这与该肿瘤类型的进展有关。在功能水平上,miR-34a-5p抑制了HNSCC细胞的增殖、迁移/侵袭活性以及上皮-间质转化诱导。在机制水平上,发现miR-34a-5p抑制FLOT-2表达并激活MEK/ERK1/2途径。总体而言,这些结果表明,miR-34a-5p因其靶向FLOT-2的能力而可作为HNSCC中的肿瘤抑制性miRNA,突出了靶向这一调控轴治疗HNSCC的前景。

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