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Oncology Reports
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Print ISSN: 1021-335X Online ISSN: 1791-2431
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November 2006 Volume 16 Issue 5

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Journals

International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

Biomedical Reports

Biomedical Reports

Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

World Academy of Sciences Journal

World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

International Journal of Functional Nutrition

International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

International Journal of Epigenetics

International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

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Medicine International

An International Open Access Journal Devoted to General Medicine.

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November 2006 Volume 16 Issue 5

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Article

Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells

  • Authors:
    • Sung Jin Kim
    • Han Saem Lee
    • June Ho Shin
    • Chul Geun Kim
    • Sunjoo Jeong
    • Keerang Park
    • Han Choe
    • Heuiran Lee
  • View Affiliations / Copyright

    Affiliations: Department of Microbiology, University of Ulsan College of Medicine, 138-736 Seoul, Korea
  • Pages: 975-979
    |
    Published online on: November 1, 2006
       https://doi.org/10.3892/or.16.5.975
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Abstract

Although the human telomerase reverse transcriptase (hTERT) promoter can regulate cancer-specific genes, it is generally too weak to be effective. We therefore attempted to improve the potency of synthetic hTERT promoters by fusing the core element (E) of the hTERT promoter (H) and the tripartite leader sequence (T) from human adenovirus 5 in a combinatorial manner. To determine the potential as cancer-specific promoters, we measured luciferase activity driven by the chimeric hTERT promoters in human cancer cells. Among various constructs, the E3-H-T promoter induced the strongest luciferase activity in all the tested cancer cells. SK-Hep1 and Hela cells experienced 1000- and 11-fold higher expression than the basic hTERT promoter, respectively. Relative to the SV40 universal promoter, the E3-H-T promoter led to higher levels of gene expression. Using EMSA, we found that the hTERT enhancer region was specifically bound to c-Myc and Sp1. Thus, the data suggest that the E3-H-T promoter with up-regulated cancer-specific gene expression could be useful in cancer gene therapy.

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Copy and paste a formatted citation
Spandidos Publications style
Kim SJ, Lee HS, Shin JH, Kim CG, Jeong S, Park K, Choe H and Lee H: Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells. Oncol Rep 16: 975-979, 2006.
APA
Kim, S.J., Lee, H.S., Shin, J.H., Kim, C.G., Jeong, S., Park, K. ... Lee, H. (2006). Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells. Oncology Reports, 16, 975-979. https://doi.org/10.3892/or.16.5.975
MLA
Kim, S. J., Lee, H. S., Shin, J. H., Kim, C. G., Jeong, S., Park, K., Choe, H., Lee, H."Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells". Oncology Reports 16.5 (2006): 975-979.
Chicago
Kim, S. J., Lee, H. S., Shin, J. H., Kim, C. G., Jeong, S., Park, K., Choe, H., Lee, H."Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells". Oncology Reports 16, no. 5 (2006): 975-979. https://doi.org/10.3892/or.16.5.975
Copy and paste a formatted citation
x
Spandidos Publications style
Kim SJ, Lee HS, Shin JH, Kim CG, Jeong S, Park K, Choe H and Lee H: Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells. Oncol Rep 16: 975-979, 2006.
APA
Kim, S.J., Lee, H.S., Shin, J.H., Kim, C.G., Jeong, S., Park, K. ... Lee, H. (2006). Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells. Oncology Reports, 16, 975-979. https://doi.org/10.3892/or.16.5.975
MLA
Kim, S. J., Lee, H. S., Shin, J. H., Kim, C. G., Jeong, S., Park, K., Choe, H., Lee, H."Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells". Oncology Reports 16.5 (2006): 975-979.
Chicago
Kim, S. J., Lee, H. S., Shin, J. H., Kim, C. G., Jeong, S., Park, K., Choe, H., Lee, H."Preferentially enhanced gene expression from a synthetic human telomerase reverse transcriptase promoter in human cancer cells". Oncology Reports 16, no. 5 (2006): 975-979. https://doi.org/10.3892/or.16.5.975
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