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Research ArticleExperimental Studies

Cathepsin L Affects Apoptosis of Glioblastoma Cells: a Potential Implication in the Design of Cancer Therapeutics

IRENA ZAJC, IRENA HRELJAC and TAMARA LAH
Anticancer Research September 2006, 26 (5A) 3357-3364;
IRENA ZAJC
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  • For correspondence: irena.zajc{at}nib.si
IRENA HRELJAC
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TAMARA LAH
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Abstract

Background: Previous studies indicate that Cathepsin L (CatL) is involved in brain tumour progression. Here, CatL in tumour cell invasion and apoptosis has been studied. Materials and Methods: Human glioblastoma cell line U87 was transfected with CatL cDNA in sense and antisense orientations. The in vitro invasiveness was tested in modified Boyden chambers. Apoptosis was determined by fluorescent staining, caspase activity, and by Bax and Bcl-2 mRNA levels. Results: Surprisingly, the invasiveness of U87 cells was not impaired by genetic down-regulation of CatL expression. In the CatL antisense clones, the apoptotic rate induced by either intrinsic or extrinsic stimuli was increased, whereas CatL sense transfection seemed to protect the cells from apoptosis. Conclusion: Increased chemoresistance of tumour cells may be associated with increased levels of CatL and may have potential application in gene therapy, which would augment the apoptosis of glioblastoma cells induced by chemotherapy.

  • Apoptosis
  • cathepsin
  • glioma
  • gene therapy
  • invasion
  • U87 cell line

Footnotes

  • Received April 14, 2006.
  • Revision received July 4, 2006.
  • Accepted July 7, 2006.
  • Copyright© 2006 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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Anticancer Research
Vol. 26, Issue 5A
September-October 2006
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Cathepsin L Affects Apoptosis of Glioblastoma Cells: a Potential Implication in the Design of Cancer Therapeutics
IRENA ZAJC, IRENA HRELJAC, TAMARA LAH
Anticancer Research Sep 2006, 26 (5A) 3357-3364;

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Cathepsin L Affects Apoptosis of Glioblastoma Cells: a Potential Implication in the Design of Cancer Therapeutics
IRENA ZAJC, IRENA HRELJAC, TAMARA LAH
Anticancer Research Sep 2006, 26 (5A) 3357-3364;
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