MicroRNA-181 targets Yin Yang 1 expression and inhibits cervical cancer progression

Mol Med Rep. 2015 Jun;11(6):4541-6. doi: 10.3892/mmr.2015.3324. Epub 2015 Feb 10.

Abstract

Dysregulated expression of microRNAs (miRNAs) has been observed in numerous types of human cancer, including cervical cancer (CC). The present study aimed to elucidate the expression and roles of miR‑181 in cervical cancer tissues and cells. HeLa cells with a stable overexpression of miR‑181 were generated and injected subcutaneously into the front legs of nude mice. Functional assays revealed a reduced rate of proliferation and an enhanced rate of apoptosis following transfection of CC cells with miR‑181 mimics. In addition, miR‑181 also suppressed tumor growth in the nude mice. At the molecular level, it was found that Yin Yang 1, an oncogene in several types of human cancer, was negatively regulated by miR‑181. Therefore, the findings of the present study suggest that exogenous overexpression of miR‑181 may be a potential approach for the treatment of CC in the future.

MeSH terms

  • 3' Untranslated Regions
  • Animals
  • Base Sequence
  • Cell Proliferation / drug effects
  • Disease Progression
  • Down-Regulation / drug effects
  • Female
  • G1 Phase Cell Cycle Checkpoints / drug effects
  • HeLa Cells
  • Humans
  • Interleukin-1beta / pharmacology
  • Interleukin-6 / pharmacology
  • Mice
  • Mice, Nude
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / metabolism*
  • Oligonucleotides, Antisense / metabolism
  • Sequence Alignment
  • Transplantation, Heterologous
  • Tumor Necrosis Factor-alpha / pharmacology
  • Uterine Cervical Neoplasms / genetics
  • Uterine Cervical Neoplasms / pathology*
  • YY1 Transcription Factor / chemistry
  • YY1 Transcription Factor / genetics
  • YY1 Transcription Factor / metabolism*

Substances

  • 3' Untranslated Regions
  • Interleukin-1beta
  • Interleukin-6
  • MicroRNAs
  • Oligonucleotides, Antisense
  • Tumor Necrosis Factor-alpha
  • YY1 Transcription Factor