Abstract

BackgroundThe microRNAs present a class of non-coding RNAs which are usually implicated in tumor biology. Recent report has unraveled that a novel member of microRNA family called miR-1246. However, the functional role and molecular mechanisms of miR-1246 in non-small cell lung cancer (NSCLC) is still elusive.MethodsUsing RT-PCR, luciferase reporter, mRNA microarrays, invasion and migration assays, we investigated the potential role of miR-1246 in the pathogenesis of NSCLC.ResultsIn this study, we showed that miR-1246 markedly promoted NSCLC cell migration and invasion. Meanwhile, we found that cytoplasmic polyadenylation element binding protein 4 (CPEB4) might be involved and serve as a direct target of miR-1246 in NSCLC. CPEB4 knockdown substantially enhanced NSCLC migration and invasion resembling the effect of miR-1246 in NSCLC. CPEB4 is also frequently downregulated in NSCLC and decreased CPEB4 expression correlated with poor survival.ConclusionsThese results suggested that the miR-1246 may promote cell metastasis by targeting CPEB4. Meanwhile, the level of CPEB4 could be used as a potential marker in NSCLC patients. Our findings unraveled novel functions of miR-1246 in lung cancer cells and shed light on NSCLC prognosis.Electronic supplementary materialThe online version of this article (doi:10.1186/s13000-015-0366-1) contains supplementary material, which is available to authorized users.

Highlights

  • The microRNAs present a class of non-coding RNAs which are usually implicated in tumor biology.T Recent report has unraveled that a novel member of microRNA family called miR-1246

  • These results suggested that the miR-1246 may promote cell metastasis by targeting cytoplasmic polyadenylation element binding protein 4 (CPEB4)

  • E the level of CPEB4 could be used as a potential marker in non-small cell lung cancer (NSCLC) patients

Read more

Summary

Methods

Using RT-PCR, luciferase reporter, mRNA microarrays, invasion and migration assays, we investigated the potential role of miR-1246 in the pathogenesis of NSCLC. We showed that miR-1246 markedly promoted NSCLC cell migration and invasion. We found that cytoplasmic polyadenylation element binding protein 4 (CPEB4) might be involved and serve as a direct target of miR-1246 in NSCLC. CPEB4 knockdown substantially enhanced NSCLC migration and invasion resembling the effect of miR-1246 in NSCLC. NSCLC tumor samples and noncancerous adjacent tissues (NAT, at least 3 cm from the tumor) were obtained from. C the surgical specimen archives of the TCM-Integrated. A approved by the Ethical Committee of TCM-Integrated. Southern Medical University, and every patient had written informed consent, the study methodologies. All lung cancer cell lines were purchased from Shanghai. Transfection was carried out and evaluated as described pre- Rviously [20]

Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call