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Oncology Reports
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Print ISSN: 1021-335X Online ISSN: 1791-2431
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January 1996 Volume 3 Issue 1

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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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Article

Basic mutant Max reverses a c-Myc block to differentiation

  • Authors:
    • C Cultraro
    • T Cogliati
    • L Hearing
    • S Segal
  • View Affiliations / Copyright

    Affiliations: NCI,NAVY MED ONCOL BRANCH,BETHESDA,MD 20889. UNIFORMED SERV UNIV HLTH SCI,BETHESDA,MD 20889.
  • Pages: 141-146
    |
    Published online on: January 1, 1996
       https://doi.org/10.3892/or.3.1.141
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Abstract

Murine erythroleukemia (MEL) cells overexpressing a transfected c-myc gene are blocked in their ability to undergo inducer-mediated differentiation, whereas overexpression of a transfected max gene mutated within the basic region (bm-max) accelerates differentiation. Based on these findings, we cotransfected MEL cells with plasmids which express human c-Myc constitutively and bm-Max in a zinc-inducible manner. Competition of endogenous proteins for binding to bm-Max can be considered negligible in cells expressing such high constitutive levels of c-Myc. Thus, this system provides a cell culture model for studying Myc:Max complex formation and its effect on erythroid differentiation. Clones expressing high levels of c-Myc and low levels of bm-Max are blocked in their ability to undergo N,N'-hexamethylene bisacetamide (HMBA)-mediated differentiation, presumably due to a preponderance of growth-promoting Myc:Max complexes. However, increased expression of bm-Max, in these clones, allows differentiation to occur by decreasing the levels of functional Myc:Max complexes. Although the exogenously expressed c-Myc and bm-Max associate in vivo, the basic region mutation in bm-Max abolishes the binding of Myc:bm-Max complexes to the specific E-box consensus sequence. We demonstrate that this sequestering of c-Myc by bm-Max reverses the c-Myc block to differentiation.

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Copy and paste a formatted citation
Spandidos Publications style
Cultraro C, Cogliati T, Hearing L and Segal S: Basic mutant Max reverses a c-Myc block to differentiation. Oncol Rep 3: 141-146, 1996.
APA
Cultraro, C., Cogliati, T., Hearing, L., & Segal, S. (1996). Basic mutant Max reverses a c-Myc block to differentiation. Oncology Reports, 3, 141-146. https://doi.org/10.3892/or.3.1.141
MLA
Cultraro, C., Cogliati, T., Hearing, L., Segal, S."Basic mutant Max reverses a c-Myc block to differentiation". Oncology Reports 3.1 (1996): 141-146.
Chicago
Cultraro, C., Cogliati, T., Hearing, L., Segal, S."Basic mutant Max reverses a c-Myc block to differentiation". Oncology Reports 3, no. 1 (1996): 141-146. https://doi.org/10.3892/or.3.1.141
Copy and paste a formatted citation
x
Spandidos Publications style
Cultraro C, Cogliati T, Hearing L and Segal S: Basic mutant Max reverses a c-Myc block to differentiation. Oncol Rep 3: 141-146, 1996.
APA
Cultraro, C., Cogliati, T., Hearing, L., & Segal, S. (1996). Basic mutant Max reverses a c-Myc block to differentiation. Oncology Reports, 3, 141-146. https://doi.org/10.3892/or.3.1.141
MLA
Cultraro, C., Cogliati, T., Hearing, L., Segal, S."Basic mutant Max reverses a c-Myc block to differentiation". Oncology Reports 3.1 (1996): 141-146.
Chicago
Cultraro, C., Cogliati, T., Hearing, L., Segal, S."Basic mutant Max reverses a c-Myc block to differentiation". Oncology Reports 3, no. 1 (1996): 141-146. https://doi.org/10.3892/or.3.1.141
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