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Information Journal Paper

Title

A BRIEF REVIEW ON THE MOLECULAR BASIS OF MEDULLARY THYROID CARCINOMA

Pages

  485-492

Abstract

 Approximately 5-10% of all thyroid cancers are MEDULLARY THYROID CARCINOMAs (MTC). MTC is mainly sporadic in nature, but 20-30% of cases are hereditary. Genetic testing for hereditary MTC is very important for the patient and his family, but the patients must be receiving appropriate genetic counseling. About 98% of patients with hereditary MTC have germline mutations in exons 10, 11, 13, 14, 15, 16 and intron 16 of the RE arrangement during transfection (RET) proto-oncogene, but the etiology of the more frequent sporadic form of MTC (sMTC) is not well understood. Recently, it has been reported that apparently sporadic MTC may involve point mutations in BRAF and RAS genes, with an overall prevalence of almost 10%. Also alteration and abnormal expression of MI RNA has been described in MTC. In this review, we attempted to mention some mutations and molecular changes in sporadic and hereditary MTC pathogenesis.

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    Cite

    APA: Copy

    MOHAMMADI, MASOUMEH, & HEDAYATI, MEHDI. (2017). A BRIEF REVIEW ON THE MOLECULAR BASIS OF MEDULLARY THYROID CARCINOMA. CELL JOURNAL (YAKHTEH), 18(4), 485-492. SID. https://sid.ir/paper/686066/en

    Vancouver: Copy

    MOHAMMADI MASOUMEH, HEDAYATI MEHDI. A BRIEF REVIEW ON THE MOLECULAR BASIS OF MEDULLARY THYROID CARCINOMA. CELL JOURNAL (YAKHTEH)[Internet]. 2017;18(4):485-492. Available from: https://sid.ir/paper/686066/en

    IEEE: Copy

    MASOUMEH MOHAMMADI, and MEHDI HEDAYATI, “A BRIEF REVIEW ON THE MOLECULAR BASIS OF MEDULLARY THYROID CARCINOMA,” CELL JOURNAL (YAKHTEH), vol. 18, no. 4, pp. 485–492, 2017, [Online]. Available: https://sid.ir/paper/686066/en

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