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靶向miR-185-3p通过调节RAB25抑制头颈部鳞状细胞癌

Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25.

作者信息

Wang Xueping, Zhu Xiaoyuan, Zhao Yulin

机构信息

Department of Otolaryngology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Front Oncol. 2021 Nov 15;11:721416. doi: 10.3389/fonc.2021.721416. eCollection 2021.

Abstract

Cancer cell-derived exosomes regulate tumor growth and progression. However, the effects of exosomes and its contents on head and neck squamous cell carcinoma (HNSCC) and its underlying mechanisms remain unclear. Here, we found HNSCC displayed a dysregulation of exosomes biogenesis. miR-185-3p was one of the most upregulated exosome-derived miRNAs in HNSCC. Functional assay showed that RAB25 is a direct downstream target of miR-185-3p. miR-185-3p/RAB25 signaling controlled tumor progression and correlated with disease prognosis. Targeting miR-185-3p/RAB25 significantly inhibited tumor growth and promoted drug response to chemotherapy. To conclude, the findings demonstrate exosomal miR-185-3p promotes tumor growth by mediating RAB25 that could be effectively targeted for HNSCC treatment.

摘要

癌细胞衍生的外泌体调节肿瘤的生长和进展。然而,外泌体及其内容物对头颈部鳞状细胞癌(HNSCC)的影响及其潜在机制仍不清楚。在此,我们发现HNSCC表现出外泌体生物发生的失调。miR-185-3p是HNSCC中上调最明显的外泌体衍生miRNA之一。功能分析表明,RAB25是miR-185-3p的直接下游靶点。miR-185-3p/RAB25信号传导控制肿瘤进展并与疾病预后相关。靶向miR-185-3p/RAB25可显著抑制肿瘤生长并促进对化疗的药物反应。总之,这些发现表明外泌体miR-185-3p通过介导RAB25促进肿瘤生长,而RAB25可作为HNSCC治疗的有效靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a032/8634093/7b9aac0198c8/fonc-11-721416-g001.jpg

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