Secretion of thymidine kinase to increase the effectivity of suicide gene therapy results in the loss of enzymatic activity

Beerens, A. M. J., Rots, M. G., Bermudez, B., De Vries, E. F. J. & Haisma, H. J., 2008, In : Journal of Drug Targeting. 16, 1, p. 26-35 10 p.

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Low efficiency of gene transfer is one of the major limitations of gene therapy. A solution to this problem may be transmission; by modification of the transgene, the gene product can be secreted and internalized by the surrounding cells. Cancer gene therapy using the herpes simplex thymidine kinase (HSV-TK) suicide gene is a promising treatment, and TK has been used in clinical trials with some success. However, this kind of therapy has limited efficacy due to the low level of gene transfer reached. A modified TK protein, capable of migrating from the producing cell to neighboring cells, would result in a greater proportion of cells affected by the treatment. As a first step towards transmission, we constructed a secretory form of HSV-TK by including the Ig leader peptide in the gene. An endoplasmatic reticulum export signal was added to the construct to further improve its secretion. Secretion and protein production in cancer cells, the enzymatic activity of the modified proteins and the ability of the modified TK to sensitize cancer cells to ganciclovir were tested. Addition of the Ig leader resulted in high levels of secretion of HSV-TK, with up to 70% of the total amount of protein secreted. Inclusion of an ER export signal did not further improve secretion. The enzyme activity of the secreted TK however, was decreased when compared to native TK. This study is the first to report on secretion of TK, and provides a first step in a novel strategy to improve the efficiency of cancer gene therapy. The loss of function in secreted TK however, may present a major hurdle in the development of a transmitted form of TK.

Original languageEnglish
Pages (from-to)26-35
Number of pages10
JournalJournal of Drug Targeting
Issue number1
Publication statusPublished - 2008


  • thymidine kinase, suicide gene therapy, cancer gene therapy, enzymatic activity, ADENOVIRAL VECTOR, INTERCELLULAR TRAFFICKING, GLUCURONIDE PRODRUG, FUSION PROTEIN, TUMOR-CELLS, FIBER KNOB, ER EXPORT, IN-VITRO, CANCER, VP22

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