[Effects of heparanase inhibition by RNA interference on proliferation, invasiveness and apoptosis of lung cancer cells]

Zhonghua Bing Li Xue Za Zhi. 2008 Dec;37(12):826-30.
[Article in Chinese]

Abstract

Objective: To investigate the effects of heparanase expression inhibition on the proliferation, invasiveness and apoptosis of human lung adenocarcinoma cell line A549 cells.

Methods: Recombinant eukaryotic expression plasmid pshRNA-Hpa targeting human heparanase gene was constructed. A549 cells were cultured in DMEM and transfected with pshRNA-Hpa. The expression of heparanase mRNA and protein were examined by RT-PCR and Western blot. The proliferation, invasiveness and apoptotic rates of A549 cells were determined by MTT method, matrigel invasion assays and flow cytometry respectively.

Results: The expression levels of heparanase mRNA and protein were down-regulated in A549 transfected with pshRNA-Hpa. The number of cells penetrating matrigel and the proliferation ability of A549 cells transfected with pshRNA-Hpa were reduced significantly compared to the control cells. The apoptotic rate of A549 cells transfected with pshRNA-Hpa was 12.53% +/- 0.34%, being significantly higher than that of the control cells (both P < 0.01). Western-blot showed that inhibition of heparanase expression led to reduced Akt phosphorylation.

Conclusions: The recombinant plasmid pshRNA-Hpa effectively inhibited the expression of heparanase, thus suppressing the proliferation and invasion and inducing apoptosis of A549 cells. The effects may be due to the down-regulation of Akt phosphorylation level.

Publication types

  • English Abstract

MeSH terms

  • Adenocarcinoma / pathology
  • Apoptosis / drug effects*
  • Carcinoma, Non-Small-Cell Lung / pathology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Down-Regulation
  • Glucuronidase / antagonists & inhibitors*
  • Glucuronidase / metabolism
  • Humans
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / pathology*
  • RNA Interference / immunology*
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / pharmacology*
  • Transfection

Substances

  • RNA, Messenger
  • RNA, Small Interfering
  • heparanase
  • Glucuronidase