4.7 Article

Circular RNA circCORO1C promotes laryngeal squamous cell carcinoma progression by modulating the let-7c-5p/PBX3 axis

期刊

MOLECULAR CANCER
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12943-020-01215-4

关键词

circCORO1C; Let-7c-5p; PBX3; Laryngeal squamous cell carcinoma; Epithelial-mesenchymal transition; Metastasis

资金

  1. National Natural Science Foundation of China [81872210, 81802793, 81802948]
  2. Postdoctoral Research Foundation of China [2016 M591412, 2017 M610174]
  3. Excellent talent science and technology innovation project of Shanxi Province [201605D211029, 201705D211018, 201805D211007]
  4. Youth Science and Technology Research Fund of Shanxi Province [201901D211486, 201901D211490]
  5. Shanxi Province Scientific and Technological Achievements Transformation Guidance Foundation [201604D131002, 201604D132040, 201804D131043]
  6. Youth Foundation of The First Hospital
  7. Shanxi Medical University [YQ1503]
  8. Youth Top Talent Program Fund of Shanxi Province
  9. Fund of Shanxi 1331 Project

向作者/读者索取更多资源

Background Laryngeal squamous cell carcinoma (LSCC) is a common malignant tumor of the head and neck. LSCC patients have seriously impaired vocal, respiratory, and swallowing functions with poor prognosis. Circular RNA (circRNA) has attracted great attention in cancer research. However, the expression patterns and roles of circRNAs in LSCC remain largely unknown. Methods RNA sequencing was performed on 57 pairs of LSCC and matched adjacent normal mucosa tissues to construct circRNA, miRNA, and mRNA expression profiles. RT-PCR, qPCR, Sanger sequencing, and FISH were undertaken to study the expression, localization, and clinical significance of circCORO1C in LSCC tissues and cells. The functions of circCORO1C in LSCC were investigated by RNAi-mediated knockdown, proliferation analysis, EdU staining, colony formation assay, Transwell assay, and apoptosis analysis. The regulatory mechanisms among circCORO1C, let-7c-5p, and PBX3 were investigated by luciferase assay, RNA immunoprecipitation, western blotting, and immunohistochemistry. Results circCORO1C was highly expressed in LSCC tissues and cells, and this high expression was closely associated with the malignant progression and poor prognosis of LSCC. Knockdown of circCORO1C inhibited the proliferation, migration, invasion, and in vivo tumorigenesis of LSCC cells. Mechanistic studies revealed that circCORO1C competitively bound to let-7c-5p and prevented it from decreasing the level of PBX3, which promoted the epithelial-mesenchymal transition and finally facilitated the malignant progression of LSCC. Conclusions circCORO1C has an oncogenic role in LSCC progression and may serve as a novel target for LSCC therapy. circCORO1C expression has the potential to serve as a novel diagnostic and prognostic biomarker for LSCC detection.

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