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International Journal of Oncology
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Print ISSN: 1019-6439 Online ISSN: 1791-2423
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September 1993 Volume 3 Issue 3

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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.

Medicine International

Medicine International

An International Open Access Journal Devoted to General Medicine.

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September 1993 Volume 3 Issue 3

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FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS

  • Authors:
    • B TARODI
    • T SUBRAMANIAN
    • G CHINNADURAI
  • View Affiliations / Copyright

    Affiliations: ST LOUIS UNIV,MED CTR,INST MOLEC VIROL,3681 PK AVE,ST LOUIS,MO 63110.
  • Pages: 467-472
    |
    Published online on: September 1, 1993
       https://doi.org/10.3892/ijo.3.3.467
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Abstract

Adenovirus mutants defective in a 19 kD protein (19K gene) encoded by the early region E1B induce DNA fragmentation in a manner similar to the internucleosomal DNA fragmentation observed during programmed cell death (apoptosis) induced by a number of chemical, physical and biological stimuli. Zn++ ions effectively suppressed DNA fragmentation induced by a 19K mutant consistent with their inhibition of DNA fragmentation during apoptosis. Since the cellular proto-oncogene Bcl2 has been shown to suppress DNA fragmentation and the resulting programmed cell death, we have carried out a functional complementation analysis to determine whether the E1B 19 kD protein is functionally similar to the Bcl2 protein. Our results indicate that the DNA fragmentation induced by the 19K mutant can be efficiently suppressed by stable expression of human Bcl2 protein. Further, the 19 kD and Bcl2 proteins also function similarly to suppress DNA fragmentation and cell death induced by the DNA damaging agents cisplatin and UV.

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Copy and paste a formatted citation
Spandidos Publications style
TARODI B, SUBRAMANIAN T and CHINNADURAI G: FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS. Int J Oncol 3: 467-472, 1993.
APA
TARODI, B., SUBRAMANIAN, T., & CHINNADURAI, G. (1993). FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS. International Journal of Oncology, 3, 467-472. https://doi.org/10.3892/ijo.3.3.467
MLA
TARODI, B., SUBRAMANIAN, T., CHINNADURAI, G."FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS". International Journal of Oncology 3.3 (1993): 467-472.
Chicago
TARODI, B., SUBRAMANIAN, T., CHINNADURAI, G."FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS". International Journal of Oncology 3, no. 3 (1993): 467-472. https://doi.org/10.3892/ijo.3.3.467
Copy and paste a formatted citation
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Spandidos Publications style
TARODI B, SUBRAMANIAN T and CHINNADURAI G: FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS. Int J Oncol 3: 467-472, 1993.
APA
TARODI, B., SUBRAMANIAN, T., & CHINNADURAI, G. (1993). FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS. International Journal of Oncology, 3, 467-472. https://doi.org/10.3892/ijo.3.3.467
MLA
TARODI, B., SUBRAMANIAN, T., CHINNADURAI, G."FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS". International Journal of Oncology 3.3 (1993): 467-472.
Chicago
TARODI, B., SUBRAMANIAN, T., CHINNADURAI, G."FUNCTIONAL SIMILARITY BETWEEN ADENOVIRUS E1B 19K GENE AND BCL2 ONCOGENE - MUTANT COMPLEMENTATION AND SUPPRESSION OF CELL-DEATH INDUCED BY DNA-DAMAGING AGENTS". International Journal of Oncology 3, no. 3 (1993): 467-472. https://doi.org/10.3892/ijo.3.3.467
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