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

Persian Verion

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:

881
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

APOPTOTIC EFFECT OF SPECIFIC SIRNA AGAINST HMGA2 ON PC3 PROSTATE ADENOCARCINOMA CELL LINE

Pages

  159-168

Keywords

PC3Q3

Abstract

 Background & objectives: Prostate cancer is one of the main reasons of death between men.Although there are many methods for treatment of this cancer but most of the patients still are died of the postoperative recurrence and metastasis of disease. Over expression of HMGA2 gene was observed in many human malignancies such as colorectal cancer, thyroid, pancreatic carcinoma and lung cancers. The aim of this study was to investigate the effect of HMGA2 specific small interfering RNAs (siRNAs) on viability and APOPTOSIS in PC3 prostate adenocarcinoma cell line.Methods: SIRNA transfection was performed with liposome approach. The CYTOTOXIC effects of SIRNA were determined using MTT assay on the PC3 cells and APOPTOSIS was quantified using TUNEL assay.Results: Transfection with SIRNA significantly suppressed the expression of HMGA2 gene in dose dependent manner after 48 hours resulting in spontaneous APOPTOSIS. Moreover, SIRNA transfection had effects on prostate cancer cells viability.Conclusion: Our results suggest that the HMGA2 specific SIRNA effectively decreases prostate cancer cells viability and induces APOPTOSIS in this cell line. Therefore it can be considered as a potent adjuvant in prostate cancer therapy.

Cites

  • No record.
  • References

    Cite

    APA: Copy

    KHAJOUEE RAVARI, SH., & BARADARAN, B.. (2016). APOPTOTIC EFFECT OF SPECIFIC SIRNA AGAINST HMGA2 ON PC3 PROSTATE ADENOCARCINOMA CELL LINE. JOURNAL OF ARDABIL UNIVERSITY OF MEDICAL SCIENCES (JAUMS), 16(2), 159-168. SID. https://sid.ir/paper/60096/en

    Vancouver: Copy

    KHAJOUEE RAVARI SH., BARADARAN B.. APOPTOTIC EFFECT OF SPECIFIC SIRNA AGAINST HMGA2 ON PC3 PROSTATE ADENOCARCINOMA CELL LINE. JOURNAL OF ARDABIL UNIVERSITY OF MEDICAL SCIENCES (JAUMS)[Internet]. 2016;16(2):159-168. Available from: https://sid.ir/paper/60096/en

    IEEE: Copy

    SH. KHAJOUEE RAVARI, and B. BARADARAN, “APOPTOTIC EFFECT OF SPECIFIC SIRNA AGAINST HMGA2 ON PC3 PROSTATE ADENOCARCINOMA CELL LINE,” JOURNAL OF ARDABIL UNIVERSITY OF MEDICAL SCIENCES (JAUMS), vol. 16, no. 2, pp. 159–168, 2016, [Online]. Available: https://sid.ir/paper/60096/en

    Related Journal Papers

    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