Long non-coding RNA HOTTIP promotes hypoxia-induced glycolysis through targeting miR-615-3p/HMGB3 axis in non-small cell lung cancer cells

• Published in: European journal of pharmacology 2019-11, Vol.862, p.172615-172615, Article 172615
• Main Authors: Shi, Jiang, Wang, Huan, Feng, Wanlu, Huang, Siyuan, An, Jinlu, Qiu, Yajuan, Wu, Kai
• Format: Article
• Language: English
• Subjects: A549 Cells; Carcinoma, Non-Small-Cell Lung - genetics; Carcinoma, Non-Small-Cell Lung - pathology; Cell Hypoxia - genetics; Down-Regulation; Gene Expression Regulation, Neoplastic; Glucose - metabolism; Glycolysis; Glycolysis - genetics; HMGB3; HMGB3 Protein - genetics; HMGB3 Protein - metabolism; HOXA transcript at the distal tip (HOTTIP); Humans; Hypoxia; Lung; Lung Neoplasms - genetics; Lung Neoplasms - pathology; MicroRNAs - genetics; MicroRNAs - metabolism; miR-615-3p; NSCLC; RNA, Long Noncoding - metabolism; Up-Regulation
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/j.ejphar.2019.172615

Increased glycolysis under hypoxic stress is a fundamentally important feature of non-small cell lung cancer (NSCLC) cells, but molecular mechanisms of hypoxia on glycolysis remain elusive. Herein, we aimed to explore whether lncRNAs and miRNAs are involved in the glycolytic reprogramming under hypoxic conditions. The levels of HOXA transcript at the distal tip (HOTTIP), miR-615-3p and high mobility group box 3 (HMGB3) mRNA were assessed by qRT-PCR. Western blot was performed to determine the protein expression of hexokinase 2 (HK-2) and HMGB3. Glucose consumption and lactate production were analyzed using a respective assay kit. The targeted correlation between miR-615-3p and HOTTIP or HMGB3 was verified using dual-luciferase reporter and RNA immunoprecipition assays. Our data revealed that HOTTIP was upregulated and miR-615-3p was downregulated in NSCLC tissues and cells. Hypoxia induced glycolysis, increased HOTTIP and HMGB3 mRNA levels and repressed miR-615-3p expression in NSCLC cells. HOTTIP deficiency or miR-615-3p expression restoration repressed hypoxia-induced glycolysis. Moreover, HOTTIP acted as a molecular sponge for miR-615-3p and HMGB3 was a direct target of miR-615-3p. The inhibitory effect of HOTTIP deficiency on glycolysis under hypoxic exposure was reversed by miR-615-3p restoration. Additionally, HOTTIP regulated HMGB3 expression by acting as a molecular sponge of miR-615-3p in NSCLC cells. In conclusion, our study suggested that HOTTIP might promote glycolysis under hypoxic conditions at least partly through regulating miR-615-3p/HMGB3 axis in NSCLC cells. Targeting HOTTIP might be a promising therapeutic strategy for NSCLC treatment.