Abstract

BackgroundPrevious studies have shown that the dysregulation of lncRNAs participates in non‐small cell lung cancer (NSCLC) development. The purpose of this study was to research the biological function of lncRNA SNHG14 and its molecular mechanism in NSCLC progression.MethodsRT‐PCR was applied for investigating the expression of SNHG14, miR‐206 and G6PD. The progression of NSCLC was detected by CCK‐8, Transwell and western blot assays. The targets of SNHG14 and miR‐206 were measured by dual‐luciferase reporter assay.ResultsWe found a higher expression of SNHG14 in NSCLC and upregulation of SNHG14 contributed to NSCLC cell proliferation, invasion and migration. However, knockdown of SNHG14 showed the opposite effect on the progression of NSCLC. Specifically, SNHG14 negatively regulated miR‐206 expression by binding with it directly. Furthermore, G6PD served as the target of miR‐206. Rescue experiments showed that SNHG14 promoted G6PD expression by inhibiting miR‐206.ConclusionsLncRNA SNHG14 contributed to NSCLC progression through miR‐206/G6PD axis, providing novel clues for understanding the mechanism of NSCLC.

Highlights

  • Lung cancer is a malignant tumor with the highest morbidity and mortality in China, which seriously threatens the life and health of people.[1,2] More than 85% of lung cancer patients are diagnosed with non-small cell lung cancer (NSCLC).[3]

  • SNHG14 was increased in NSCLC To detect the role of lncRNA SNHG14’ in NSCLC development, the expression level of SNHG14 was first measured in NSCLC tissues and cells

  • We showed that SNHG14 was highly expressed in NSCLC tissues and cells

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Summary

Introduction

Lung cancer is a malignant tumor with the highest morbidity and mortality in China, which seriously threatens the life and health of people.[1,2] More than 85% of lung cancer patients are diagnosed with non-small cell lung cancer (NSCLC).[3]. Previous studies have shown that the dysregulation of lncRNAs participates in non-small cell lung cancer (NSCLC) development. The purpose of this study was to research the biological function of lncRNA SNHG14 and its molecular mechanism in NSCLC progression. Methods: RT-PCR was applied for investigating the expression of SNHG14, miR-206 and G6PD. The targets of SNHG14 and miR-206 were measured by dual-luciferase reporter assay. Results: We found a higher expression of SNHG14 in NSCLC and upregulation of SNHG14 contributed to NSCLC cell proliferation, invasion and migration. Knockdown of SNHG14 showed the opposite effect on the progression of NSCLC. G6PD served as the target of miR-206. Rescue experiments showed that SNHG14 promoted G6PD expression by inhibiting miR-206. Conclusions: LncRNA SNHG14 contributed to NSCLC progression through miR-206/G6PD axis, providing novel clues for understanding the mechanism of NSCLC

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