مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

281
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

THE EFFECT OF EXOGENOUS EXPRESSION OF TP53 GENE CARRIED BY DENDROSOME, AN IRANIAN VECTOR ON HUMAN T-LYMPHOMAAND LEUKEMIA CELLS

Author(s)

 , , | Issue Writer Certificate 

Pages

  206-211

Abstract

 Introduction: The tumor suppressor p53 protein can induce APOPTOSIS in some cellular contexts. Among the APOPTOSIS-inducing genes, p53 has received the most attention for cancer gene therapy. In this study, the role of DENDROSOME and Lipofectin mediated normal cDNA of TP53 into MOLT-4, CCRF-CEM(T-Iymphoma) and K562 cell lines was assessed. Material and Methods: At first, CCRF-CEM, MOL T-4 and K562 (erythroleukemic) cell lines were transfetted by DENDROSOME and Lipofectin separately. Then, viability study was carried out by Trypan blue exclusion. The rate of APOPTOSIS and necrosis in transfected cell lines was evaluated by Flow Cytometry. Results: Trypan blue exclusion assay in K562 and CCRF-CEM revealed 55.8% and 17.97 % viability reduction in the Dend+p53 in comparison to Dend+pcDNA3 (control), respectively. Flow Cytometry studies confirmed a significant enhancement of APOPTOSIS and necrosis in TP53 transrected K562 and CCRF-CEM cells. Flow Cytometry and viability studies Qntransfected MOLT-4 cells showed no significant changes. Conclusion: The results showed that expression of normal cDNA of TP53 in K562 and CCRF-CEM cell lines could induce APOPTOSIS in these cell lines with different levels. Transfection of MOLT-4 cell Line by Dend+p53 and Lipo+53 could not result in APOPTOSIS.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    . (2005). THE EFFECT OF EXOGENOUS EXPRESSION OF TP53 GENE CARRIED BY DENDROSOME, AN IRANIAN VECTOR ON HUMAN T-LYMPHOMAAND LEUKEMIA CELLS. CELL JOURNAL (YAKHTEH), 6(24), 206-211. SID. https://sid.ir/paper/542224/en

    Vancouver: Copy

    . THE EFFECT OF EXOGENOUS EXPRESSION OF TP53 GENE CARRIED BY DENDROSOME, AN IRANIAN VECTOR ON HUMAN T-LYMPHOMAAND LEUKEMIA CELLS. CELL JOURNAL (YAKHTEH)[Internet]. 2005;6(24):206-211. Available from: https://sid.ir/paper/542224/en

    IEEE: Copy

    , “THE EFFECT OF EXOGENOUS EXPRESSION OF TP53 GENE CARRIED BY DENDROSOME, AN IRANIAN VECTOR ON HUMAN T-LYMPHOMAAND LEUKEMIA CELLS,” CELL JOURNAL (YAKHTEH), vol. 6, no. 24, pp. 206–211, 2005, [Online]. Available: https://sid.ir/paper/542224/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    File Not Exists.
    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button