Skip to main navigation Skip to search Skip to main content

Long non-coding RNA LINC01116 is overexpressed in lung adenocarcinoma and promotes tumor proliferation and metastasis

  • Lizhong Zeng
  • , Xin Lyu
  • , Jingyan Yuan
  • , Wei Wang
  • , Nannan Zhao
  • , Boxuan Liu
  • , Ruiying Sun
  • , Xia Meng
  • , Shuanying Yang

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Long non-coding RNA LINC01116 is involved in the occurrence and progression of a variety of cancers. However, the specific role of LINC01116 in lung adenocarcinoma (LUAD) remains unclear. In this work, we found that LINC01116 was overexpressed in LUAD tissues and cell lines and that increased expression was significantly associated with worse prognoses in patients with LUAD. Univariate and multivariate Cox regression analyses indicated that LINC01116 was an independent risk factor for the prognosis of patients with LUAD. Downregulation of LINC01116 significantly inhibited cell proliferation and migration, promoted cell apoptosis, and prevented cell progression from G1 to S phase. In addition, downregulation of LINC01116 significantly inhibited the epithelial-mesenchymal transition, leading to an increased expression of the epithelial marker E-cadherin and decreased expression of the mesenchymal markers N-cadherin and vimentin. In summary, our results suggest that LINC01116 may act as an oncogene in LUAD and may be a valuable prognostic biomarker for patients with LUAD.

Original languageEnglish
Pages (from-to)4302-4313
Number of pages12
JournalAmerican Journal of Translational Research
Volume12
Issue number8
StatePublished - 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • EMT
  • LINC01116
  • Lung adenocarcinoma
  • Prognosis
  • Proliferation

Fingerprint

Dive into the research topics of 'Long non-coding RNA LINC01116 is overexpressed in lung adenocarcinoma and promotes tumor proliferation and metastasis'. Together they form a unique fingerprint.

Cite this