[Inhibition of invasiveness and expression of heparanase-mRNA in human malignant melanoma cell line A375 by matrine]

Zhong Yao Cai. 2006 Mar;29(3):253-6.
[Article in Chinese]

Abstract

Objective: To investigate the effect of matrine on the invasiveness and expression of heparanase-mRNA in human malignant melanoma cell line A375.

Methods: The A375 cells were treated by matrine in different concentration. The total RNAs were extracted from the cells 48 hours after treatment and then semi-quantitative RT-PCR were performed to evaluate the heparanase-mRNA expression levels. Effect of matrine on adhesion of treated A375 cells was tested by cell-Matrigel adhesion assay. The invasiveness of treated A375 cells was measured by Matrigel invasion assay.

Results: The hepanase-mRNA expression, adhesion and invasiveness of A375 cells treated with matrine of different final concentrations significantly decreased compared with that of the controls (p < 0.01). Besides, the inhibitory effects were signifcantly different when the cells treated with matrine of different concentrations (P < 0.01).

Conclusion: By down-regulating the expression of heparanase-mRNA, matrine has a significant inhibitory effect on the adhesion and invasiveness of human malignant melanoma cell line in a dose-dependent manner.

MeSH terms

  • Alkaloids / administration & dosage
  • Alkaloids / pharmacology*
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Cell Adhesion / drug effects
  • Cell Line, Tumor
  • Dose-Response Relationship, Drug
  • Drugs, Chinese Herbal / pharmacology
  • Glucuronidase / biosynthesis*
  • Glucuronidase / genetics
  • Humans
  • Matrines
  • Melanoma / enzymology
  • Melanoma / pathology*
  • Neoplasm Invasiveness
  • Plants, Medicinal / chemistry
  • Quinolizines / administration & dosage
  • Quinolizines / pharmacology*
  • RNA, Messenger / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sophora / chemistry*

Substances

  • Alkaloids
  • Antineoplastic Agents, Phytogenic
  • Drugs, Chinese Herbal
  • Quinolizines
  • RNA, Messenger
  • heparanase
  • Glucuronidase
  • Matrines