Journal
CELL DEATH & DISEASE
Volume 10, Issue -, Pages -Publisher
SPRINGERNATURE
DOI: 10.1038/s41419-019-2154-4
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Funding
- National Key Research and Development Program of China [2017YFA0505104]
- National Natural Science Foundation of China [81772540, 81772752, 81472760, 81902771]
- Guangdong Innovative and Entrepreneurial Research Team Program [2013Y113]
- Science and Technology Program of Guangdong [2019A050510023, 2017A020215122, 2014A020212078]
- Medical Scientific Research Foundation of Guangdong Province [2018118215914106]
- Science and Technology Program of Guangzhou [201709010038, 201903010024]
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The burgeoning functions of many microRNAs (miRs) have been well study in cancer. However, the level and function of miR-1205 in laryngeal squamous cell cancer remains unknown. In the current research, we validated that miR-1205 was notably downregulated in human laryngeal squamous cell carcinoma (LSCC) samples in comparison with tissues adjacent to LSCC, and correlated with T stage, lymph node metastasis, and clinical stage. Using Kaplan-Meier analysis indicates that high expression of miR-1205 has a favorable prognosis for patients with LSCC. Functional assays show that enforced miR-1205 expression attenuates the migration, growth, and invasion of LSCC cells. And E2F1 is verified to be a target of miR-1205, while E2F1 binds to miR-1205 promoter and transcriptionally inhibits miR-1205 expression. Overexpression of E2F1 reverses the inhibitory impacts of miR-1205 on LSCC cells in part. Importantly, E2F1 is abnormally increased in LSCC tissues, and its protein levels were inversely relevant to miR-1205 expression. High E2F1 protein level is in connection with clinical stage, T stage, lymph node metastasis, and poor prognosis. Consequently, reciprocal regulation of miR-1205 and E2F1 plays a crucial role in the progression of LSCC, suggesting a new miR-1205/ E2F1-based clinical application for patients of LSCC.
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