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High Prevalence of c-RET Expression in Papillary Thyroid Carcinomas from the Korean Population

Authors
 Sihoon Lee  ;  Soon Won Hong  ;  Woo Chul Moon  ;  Myung Ryurl Oh  ;  Jin Kyung Lee  ;  Chul Woo Ahn  ;  Bong Soo Cha  ;  Kyung Rae Kim  ;  Hyun Chul Lee  ;  Sung-Kil Lim 
Citation
 Thyroid, Vol.15(3) : 259-266, 2005 
Journal Title
 Thyroid 
ISSN
 1050-7256 
Issue Date
2005
MeSH
Adenocarcinoma, Papillary/genetics* ; Adenocarcinoma, Papillary/pathology ; Asian Continental Ancestry Group/genetics ; DNA Primers ; Humans ; Immunohistochemistry ; Korea ; Prevalence ; Reverse Transcriptase Polymerase Chain Reaction ; Thyroid Gland/pathology ; Thyroid Neoplasms/genetics* ; Thyroid Neoplasms/pathology
Keywords
15785245
Abstract
Background: Activation of the RET proto-oncogene, located on the long arms of chromosome 10, contributes to the development of thyroid cancers in two different ways. First, somatic rearrangements of RET with variable activation genes are frequently found in papillary thyroid carcinomas. Second, germ-line point mutations are responsible for the development of medullary thyroid carcinomas and multiple endocrine neoplasia type 2 (MEN 2). There are several conflicting reports on the influences of RET expression and RET/PTC rearrangements on the clinical outcome of thyroid cancers. Therefore, the wild-type RET gene expression and RET/PTC-1, RET/PTC-2, RET/PTC-3 rearrangements were examined in thyroid carcinomas and other thyroid diseases. Materials and Methods: Thirty-six papillary thyroid carcinomas (PTCs), 8 follicular thyroid carcinomas (FTCs), 4 anaplastic thyroid carcinomas (ATC), 7 follicular adenomas (FAs), 23 hyperplasias, 6 normal thyroid tissues, and 39 normal portions from each tumor were included in this study. Reverse transcription-polymerase chain reaction (RT-PCR) and immunohistochemical analyses were used to identify the RET gene and RET/PTC rearrangements. Results: From the RT-PCR analysis, 68.9% of the PTCs, a single case of FTC, and 22.2% of the hyperplasias expressed the RET gene. No RET gene expression was observed in ATCs, FAs, or normal thyroid tissues. One RET/PTC-1 and one RET/PTC-2 rearrangement were detected in the PTCs. No RET/PTC-3 rearrangement was detected in any specimen. The immunohistochemical results revealed that 66.7% of PTCs, 28.6% of FAs, and 18.2% of hyperplastic thyroid tissue specimens showed high levels of RET protein expression. Neither the normal thyroid tissues nor the FTCs and ATC, showed high levels of RET protein expression. The two methods are agreed in PTC and hyperplastic nodules, but not in FA and FTC. Conclusion: PTCs among Koreans rarely showed RET/PTC rearrangements, but commonly showed increased RET gene expression. Compared to earlier reports indicating that the expression of the RET gene was limited to PTCs, the RET gene was also expressed in hyperplasias in this study.
Full Text
http://online.liebertpub.com/doi/abs/10.1089/thy.2005.15.259
DOI
10.1089/thy.2005.15.259.
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Kyung Rae(김경래)
Ahn, Chul Woo(안철우) ORCID logo https://orcid.org/0000-0003-3733-7486
Lee, Si Hoon(이시훈)
Lee, Hyun Chul(이현철)
Lim, Sung Kil(임승길)
Cha, Bong Soo(차봉수) ORCID logo https://orcid.org/0000-0003-0542-2854
Hong, Soon Won(홍순원) ORCID logo https://orcid.org/0000-0002-0324-2414
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/147484
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