Association of microRNA-181c expression with the progression and prognosis of human gastric carcinoma

Hepatogastroenterology. 2013 Jul-Aug;60(125):961-4. doi: 10.5754/hge121333.

Abstract

Background/aims: The relationship of miR-181c, a potential tumor regulatory factor, with gastric cancer is not well studied. We have investigated this relationship in our study.

Methodology: Paraffin-embedded tissue specimens from 103 gastric cancer patients were subjected to total RNA extraction. Reverse transcription real-time fluorescence quantitative PCR was used to detect miR-181c expression. Its relative expression was correlated with the patients’ clinicopathological features. Also, the 5-year survival rate and median survival time were correlated with the miR-181c expression level.

Results: miR-181c expression was significantly and directly correlated with the degree of tumor differentiation, invasive depth and clinical stage. Moreover, lymph node metastasis was significantly related with higher miR-181c expression. However, miR-181c expression was not significantly correlated with gender, age, tumor location and distant metastasis. The 5-year overall survival rate and median survival time were significantly greater in patients with low expression of miR-181c.

Conclusions: miR-181c expression level was significantly related to several clinicopathological features of gastric cancer; therefore, miR-181c probably plays a role in its development and progression. This relationship needs to be studied in detail, so that the potential use of miR-181c as a marker for gastric cancer and therapeutic target can be explored.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Disease Progression
  • Female
  • Humans
  • Lymphatic Metastasis
  • Male
  • MicroRNAs / analysis
  • MicroRNAs / physiology*
  • Middle Aged
  • Prognosis
  • Stomach Neoplasms / genetics
  • Stomach Neoplasms / mortality
  • Stomach Neoplasms / pathology*

Substances

  • MIrn181 microRNA, human
  • MicroRNAs