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

Journal Paper

Paper Information

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:

784
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

GERMLINE MUTATIONS OF RET PROTO-ONCOGENE EXON 2 IN IRANIAN POPULATION WITH MEDULLARY THYROID CARCINOMA

Pages

  636-642

Abstract

 Introduction: MEDULLARY THYROID CARCINOMA (MTC) accounts for 5-10% of all thyroid cancers andit is inherited in autosomal dominant pattern. Association of RET proto-oncogene mutations in exons 10-16 with MTC is well recognized. Since less attention has been paid to the study of other exons within the same gene, therefore, the aim of this study was to determine the frequency of germ line mutations in exon 2 of the RET proto-oncogene in patients with MTC in Iranian population.Materials and Methods: There were 223 subjects (125 patients and 98 family members) were participated n this study. Genomic DNA was extracted using standard salting out/proteinase K method. The EXON2 and exon-intron boundaries were amplified by using Polymerase Chain Reaction (PCR) and the direct DNA sequencing method was used for genotype analysis.Results: The nucleotide changes c135G>A/A45A (rs1800858) in exon 2 and c.337+9G>A (rs2435351) and c.337+137G>T (rs2505530) were found in intronic region of RET gene. Among patients and relatives, the most and least genotype and allele frequencies were c.337+137G>T (rs2505530) and c135G>A/A45A (rs1800858), respectively. Also we did not find any significant correlation between detected nucleotide changes and disease phenotype, gender and ethnicity.Conclusion: No mutation was detected leading to change in amino acid sequences in exon 2 or in exon-intron splice sites. However, further studies are recommended to identify the probable correlation between detected variations and presence or absence of other mutations in other RET main exons, and also to find haplotype association with the disease.

Cites

  • No record.
  • References

    Cite

    APA: Copy

    HESANMANESH, HOSNA, ZARIF YEGANEH, MARJAN, SHEIKHOLESLAMI, SARA, FARHUD, DARIUSH, & HEDAYATI, MEHDI. (2016). GERMLINE MUTATIONS OF RET PROTO-ONCOGENE EXON 2 IN IRANIAN POPULATION WITH MEDULLARY THYROID CARCINOMA. KOOMESH, 17(3 (59)), 636-642. SID. https://sid.ir/paper/36880/en

    Vancouver: Copy

    HESANMANESH HOSNA, ZARIF YEGANEH MARJAN, SHEIKHOLESLAMI SARA, FARHUD DARIUSH, HEDAYATI MEHDI. GERMLINE MUTATIONS OF RET PROTO-ONCOGENE EXON 2 IN IRANIAN POPULATION WITH MEDULLARY THYROID CARCINOMA. KOOMESH[Internet]. 2016;17(3 (59)):636-642. Available from: https://sid.ir/paper/36880/en

    IEEE: Copy

    HOSNA HESANMANESH, MARJAN ZARIF YEGANEH, SARA SHEIKHOLESLAMI, DARIUSH FARHUD, and MEHDI HEDAYATI, “GERMLINE MUTATIONS OF RET PROTO-ONCOGENE EXON 2 IN IRANIAN POPULATION WITH MEDULLARY THYROID CARCINOMA,” KOOMESH, vol. 17, no. 3 (59), pp. 636–642, 2016, [Online]. Available: https://sid.ir/paper/36880/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