Inhibitory effects of miR-101 overexpression on cervical cancer SiHa cells

Eur J Gynaecol Oncol. 2017;38(2):236-240.

Abstract

Purpose of investigation: microRNAs (miRNAs), which can regulate cell biological behaviors such as proliferation and apoptosis as oncogenes or anti-oncogenes, are closely associated with cancer onset and progression. The aim of this study was to detect the expres- sion changes of miR-101 in cervical cancer tissues and the effects on the biological functions of cervical cancer SiHa cells.

Materials and methods: Through transient transfection of SiHa cells with mature miR-101 sequences, the effects on apoptosis, proliferation, and cell cycle were evaluated by real-time PCR, CCK-8 assay, and flow cytometry.

Results: Significantly less miR-101 was expressed in cervical cancer tissues than that in normal cervical tissues. miR-101 was overexpressed in SiHa cells through transient transfection of miR-101 mimics. CCK-8 assay and flow cytometry showed that miR-101 overexpression significantly inhibited cell proliferation, pro- moted apoptosis, and arrested them in the G(l)/S phase. Real-time PCR exhibited that Mcl-i and c-Fos mRNA expressions significantly decreased.

Conclusion: miR-101 significantly reduced the viability of SiHa cells as a potential anti-oncogene.

MeSH terms

  • Apoptosis / genetics
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Cervix Uteri / metabolism
  • Female
  • G1 Phase Cell Cycle Checkpoints / genetics
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Myeloid Cell Leukemia Sequence 1 Protein / genetics
  • Proto-Oncogene Proteins c-fos / genetics
  • RNA, Messenger / metabolism
  • S Phase Cell Cycle Checkpoints / genetics
  • Transfection
  • Uterine Cervical Neoplasms / genetics*
  • Uterine Cervical Neoplasms / metabolism

Substances

  • MCL1 protein, human
  • MIRN101 microRNA, human
  • MicroRNAs
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Proto-Oncogene Proteins c-fos
  • RNA, Messenger