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:

775
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:

1

Information Journal Paper

Title

STUDY OF P14/ARF GENE PROMOTER METHYLATION AND EFFECT OF INTERLEUKIN-17 GENE POLYMORPHISM ON THIS METHYLATION AMONG BREAST CANCER PATIENTS

Author(s)

NAEIMI S. | Issue Writer Certificate 

Pages

  809-818

Abstract

 Background: hyper-methylation in CpG Island is one of the major mechanisms in gene silencing. In many cancers, different genes are experiencing CIHM (CpG island hyper methylation). P14 / ARF regulatory factor, involved in negative regulation of the cell cycle through the effect on P53 factor pathway. On the other hand, Interleukin 17 can be increased methylation by inflammatory effects. The purpose of this study was to study the P14/ARF gene PROMOTER METHYLATION and effect of INTERLEUKIN-17 on this methylation among BREAST CANCER patients in the south of the country and its comparison with healthy people.Materials and Methods: in this case–control study, peripheral blood of 40 patients with BREAST CANCER who were referred to hospitals in Shiraz and 40 healthy women was used to DNA extraction by using salt out and K proteinase. Control subjects with a family history of cancer or autoimmune diseases were excluded from the study. We used PCR-RFLP method In order to study of INTERLEUKIN-17 gene POLYMORPHISM, and MSPCR method was used to study of P14/ARF gene PROMOTER METHYLATION. The results of the study were studied by using SPSS software, Arlequin, chi-square and Hardy-weinberg equilibrium test was used respectively.Results: findings confirms that there was a significant association between P14/ARF gene PROMOTER METHYLATION and disease and mentioned gene promoter was less methylated in healthy subjects compared to patients (p<0.05). On the other hand, there is a significant association between GG genotype in IL17 F gene POLYMORPHISMs and P14 /ARF gene methylation (P<0.05).Conclusion: P14/ARF gene promoter’s methylation play an important role in BREAST CANCER. Due to the decline of P14P14/ARF gene promoters methylation and its association with this disease, seems that it could be used as a biomarker for diagnosis.

Cites

References

  • No record.
  • Cite

    APA: Copy

    NAEIMI, S.. (2016). STUDY OF P14/ARF GENE PROMOTER METHYLATION AND EFFECT OF INTERLEUKIN-17 GENE POLYMORPHISM ON THIS METHYLATION AMONG BREAST CANCER PATIENTS. IRANIAN SOUTH MEDICAL JOURNAL (ISMJ), 19(5), 809-818. SID. https://sid.ir/paper/33776/en

    Vancouver: Copy

    NAEIMI S.. STUDY OF P14/ARF GENE PROMOTER METHYLATION AND EFFECT OF INTERLEUKIN-17 GENE POLYMORPHISM ON THIS METHYLATION AMONG BREAST CANCER PATIENTS. IRANIAN SOUTH MEDICAL JOURNAL (ISMJ)[Internet]. 2016;19(5):809-818. Available from: https://sid.ir/paper/33776/en

    IEEE: Copy

    S. NAEIMI, “STUDY OF P14/ARF GENE PROMOTER METHYLATION AND EFFECT OF INTERLEUKIN-17 GENE POLYMORPHISM ON THIS METHYLATION AMONG BREAST CANCER PATIENTS,” IRANIAN SOUTH MEDICAL JOURNAL (ISMJ), vol. 19, no. 5, pp. 809–818, 2016, [Online]. Available: https://sid.ir/paper/33776/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • 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