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:

960
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

EVALUATION OF MDM2 AND P53 EXPRESSION IN DENTIGEROUS, RADICULAR AND RESIDUAL CYSTS BY IMMUNUHISTOCHEMISTRY

Pages

  145-152

Abstract

 Introduction: DENTIGEROUS CYST (the most common developmental cyst), periapical cyst (the most common jaw cyst) and RESIDUAL CYST may transfer to neoplasm. In this study, the expression of P53 & MDM2 (cell proliferative regulators) and their relation to proliferation and transformation of these cysts were evaluated. Materials & Methods: In this cross-sectional study, expressions of P53 and MDM2 markers in 60 samples of paraffin blocks (20 samples for each cyst) were examined by Immunohistochemistry method and the percentage, intensity, and location of involved epithelial cells were evaluated. Statistical tests included one way ANOVA and Tukey test for evaluation of expression, and Kruskal-Wallis for intensity comparison and Kendall for detecting correlation between markers.Results: Periapical cyst showed complete expression of markers. Severity, percentage and depth of MDM2 expression were higher than P53. Marker expression for RESIDUAL CYST was highly intensive and also in full thickness of epithelium, but it was basillary with lower intensity in DENTIGEROUS CYST. Expression of P53 and MDM2 had significant differences in these three cysts (P=0.01, 0.03 respectively), and also significant difference for percentage and severity of MDM2 between the three groups (P=0.003, 0.001 respectively). There was a positive linear correlation between P53 and MDM2 expression (P<0.001).Conclusion: In RESIDUAL CYST, there was a correlation between increase in MDM2and P53 expression, but not in periapical cyst. DENTIGEROUS CYST failed to strongly express each of the markers. Nevertheless, it could be said that increase in expression of these markers could be related to pathogenesis and neoplastic transformation of these cysts.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    SAGHARVANIAN, N.A., HABIBI, A.A., MOHTASHAM, N., AFZAL AGHAEI, M., SHIVA, A., & BABAZADEH, S.. (2009). EVALUATION OF MDM2 AND P53 EXPRESSION IN DENTIGEROUS, RADICULAR AND RESIDUAL CYSTS BY IMMUNUHISTOCHEMISTRY. JOURNAL OF MASHHAD DENTAL SCHOOL, 33(2 (69)), 145-152. SID. https://sid.ir/paper/73921/en

    Vancouver: Copy

    SAGHARVANIAN N.A., HABIBI A.A., MOHTASHAM N., AFZAL AGHAEI M., SHIVA A., BABAZADEH S.. EVALUATION OF MDM2 AND P53 EXPRESSION IN DENTIGEROUS, RADICULAR AND RESIDUAL CYSTS BY IMMUNUHISTOCHEMISTRY. JOURNAL OF MASHHAD DENTAL SCHOOL[Internet]. 2009;33(2 (69)):145-152. Available from: https://sid.ir/paper/73921/en

    IEEE: Copy

    N.A. SAGHARVANIAN, A.A. HABIBI, N. MOHTASHAM, M. AFZAL AGHAEI, A. SHIVA, and S. BABAZADEH, “EVALUATION OF MDM2 AND P53 EXPRESSION IN DENTIGEROUS, RADICULAR AND RESIDUAL CYSTS BY IMMUNUHISTOCHEMISTRY,” JOURNAL OF MASHHAD DENTAL SCHOOL, vol. 33, no. 2 (69), pp. 145–152, 2009, [Online]. Available: https://sid.ir/paper/73921/en

    Related Journal Papers

    Related Seminar Papers

    Related Plans

  • No record.
  • Recommended Workshops






    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