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      The Diagnostic Usefulness of HMGA2, Survivin, CEACAM6, and SFN/14-3-3 δ in Follicular Thyroid Carcinoma

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      https://www.riss.kr/link?id=A101634060

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      Background: Follicular thyroid carcinoma (FTC) is the second most common thyroid malignancy and its differential diagnosis includes follicular adenoma (FA) and adenomatous goiter (AG). Several ancillary markers have been suggested to aid in the diagnosis of FTC, but the successful use of these methods still needs to be validated. Methods: In the present study, we verified the immunoexpression of HMGA2, CEACAM6, survivin, and SFN/14-3-3 δ in lesions including 41 AGs, 72 FAs, and 79 FTCs. We evaluated their diagnostic usefulness, combined with galectin 3, Hector Battifora mesothelial 1 (HBME1), cytokeratin 19, and cyclin D1, in diagnosing FTC. Results: The expressions of HBME1 (65.8%) and HMGA2 (55.7%) were significantly higher in FTCs than in FAs and AGs (p<.001 and p=.005, respectively). HBME1 was the only marker that was more frequently expressed in FTCs than in FAs (p=.021) and it was more frequently expressed in follicular neoplasms than in AGs (p<.001). Among the novel markers, the combination of HMGA2 and HBME1 showed the highest sensitivity (72.2%) and specificity (76.1%) for diagnosing FTC. CEACAM6, survivin, and SFN/14-3-3 δ were barely expressed in most cases. Conclusions: Our present results show that only HMGA2 can be beneficial in differentiating FTC using the novel markers.
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      Background: Follicular thyroid carcinoma (FTC) is the second most common thyroid malignancy and its differential diagnosis includes follicular adenoma (FA) and adenomatous goiter (AG). Several ancillary markers have been suggested to aid in the diagno...

      Background: Follicular thyroid carcinoma (FTC) is the second most common thyroid malignancy and its differential diagnosis includes follicular adenoma (FA) and adenomatous goiter (AG). Several ancillary markers have been suggested to aid in the diagnosis of FTC, but the successful use of these methods still needs to be validated. Methods: In the present study, we verified the immunoexpression of HMGA2, CEACAM6, survivin, and SFN/14-3-3 δ in lesions including 41 AGs, 72 FAs, and 79 FTCs. We evaluated their diagnostic usefulness, combined with galectin 3, Hector Battifora mesothelial 1 (HBME1), cytokeratin 19, and cyclin D1, in diagnosing FTC. Results: The expressions of HBME1 (65.8%) and HMGA2 (55.7%) were significantly higher in FTCs than in FAs and AGs (p<.001 and p=.005, respectively). HBME1 was the only marker that was more frequently expressed in FTCs than in FAs (p=.021) and it was more frequently expressed in follicular neoplasms than in AGs (p<.001). Among the novel markers, the combination of HMGA2 and HBME1 showed the highest sensitivity (72.2%) and specificity (76.1%) for diagnosing FTC. CEACAM6, survivin, and SFN/14-3-3 δ were barely expressed in most cases. Conclusions: Our present results show that only HMGA2 can be beneficial in differentiating FTC using the novel markers.

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      참고문헌 (Reference)

      1 Saleh HA, "Utility of immunohistochemical markers in differentiating benign from malignant follicular-derived thyroid nodules" 5 : 9-, 2010

      2 de Matos PS, "Usefulness of HBME-1, cytokeratin 19 and galectin-3 immunostaining in the diagnosis of thyroid malignancy" 47 : 391-401, 2005

      3 Belge G, "Upregulation of HMGA2 in thyroid carcinomas : a novel molecular marker to distinguish between benign and malignant follicular neoplasias" 47 : 56-63, 2008

      4 Prasad NB, "Three-gene molecular diagnostic model for thyroid cancer" 22 : 275-284, 2012

      5 Sigstad E, "The new molecular markers DDIT3, STT3A, ARG2 and FAM129A are not useful in diagnosing thyroid follicular tumors" 25 : 537-547, 2012

      6 Lal G, "Regulation of 14-3-3sigma expression in human thyroid carcinoma is epigenetically regulated by aberrant cytosine methylation" 267 : 165-174, 2008

      7 Baloch ZW, "Our approach to follicular-patterned lesions of the thyroid" 60 : 244-250, 2007

      8 Mazzaferri EL, "Management of a solitary thyroid nodule" 328 : 553-559, 1993

      9 Bryson PC, "Immunohistochemical distinction of follicular thyroid adenomas and follicular carcinomas" 134 : 581-586, 2008

      10 Haghpanah V, "Immunohistochemical analysis of survivin expression in thyroid follicular adenoma and carcinoma" 14 : 422-425, 2006

      1 Saleh HA, "Utility of immunohistochemical markers in differentiating benign from malignant follicular-derived thyroid nodules" 5 : 9-, 2010

      2 de Matos PS, "Usefulness of HBME-1, cytokeratin 19 and galectin-3 immunostaining in the diagnosis of thyroid malignancy" 47 : 391-401, 2005

      3 Belge G, "Upregulation of HMGA2 in thyroid carcinomas : a novel molecular marker to distinguish between benign and malignant follicular neoplasias" 47 : 56-63, 2008

      4 Prasad NB, "Three-gene molecular diagnostic model for thyroid cancer" 22 : 275-284, 2012

      5 Sigstad E, "The new molecular markers DDIT3, STT3A, ARG2 and FAM129A are not useful in diagnosing thyroid follicular tumors" 25 : 537-547, 2012

      6 Lal G, "Regulation of 14-3-3sigma expression in human thyroid carcinoma is epigenetically regulated by aberrant cytosine methylation" 267 : 165-174, 2008

      7 Baloch ZW, "Our approach to follicular-patterned lesions of the thyroid" 60 : 244-250, 2007

      8 Mazzaferri EL, "Management of a solitary thyroid nodule" 328 : 553-559, 1993

      9 Bryson PC, "Immunohistochemical distinction of follicular thyroid adenomas and follicular carcinomas" 134 : 581-586, 2008

      10 Haghpanah V, "Immunohistochemical analysis of survivin expression in thyroid follicular adenoma and carcinoma" 14 : 422-425, 2006

      11 Prasad NB, "Identification of genes differentially expressed in benign versus malignant thyroid tumors" 14 : 3327-3337, 2008

      12 Wiseman SM, "Hemithyroidectomy : the optimal initial surgical approach for individuals undergoing surgery for a cytological diagnosis of follicular neoplasm" 13 : 425-432, 2006

      13 Chiappetta G, "HMGA2 mRNA expression correlates with the malignant phenotype in human thyroid neoplasias" 44 : 1015-1021, 2008

      14 Prasad ML, "Galectin-3, fibronectin-1, CITED-1, HBME1 and cytokeratin-19 immunohistochemistry is useful for the differential diagnosis of thyroid tumors" 18 : 48-57, 2005

      15 Papale F, "Galectin-3 expression in thyroid fine needle cytology (t-FNAC) uncertain cases: validation of molecular markers and technology innovation" 228 : 968-974, 2013

      16 LiVolsi VA, "Follicular-patterned tumors of the thyroid: the battle of benign vs. malignant vs. so-called uncertain" 22 : 184-189, 2011

      17 Sobrinho-Simões M, "Follicular thyroid carcinoma" 24 (24): S10-S18, 2011

      18 Kapur U, "Follicular neoplasm of the thyroid: vanishing cytologic diagnosis?" 35 : 525-528, 2007

      19 McHenry CR, "Follicular adenoma and carcinoma of the thyroid gland" 16 : 585-593, 2011

      20 박영주, "Diagnostic Value of Galectin-3, HBME-1, Cytokeratin 19, HighMolecular Weight Cytokeratin, Cyclin D1 and p27kip1 in the DifferentialDiagnosis of Thyroid Nodules" 대한의학회 22 (22): 621-628, 2007

      21 Cerutti JM, "Diagnosis of suspicious thyroid nodules using four protein biomarkers" 12 (12): 3311-3318, 2006

      22 김영아, "Detection of Survivin and COX-2 in Thyroid Carcinoma: Anaplastic Carcinoma Shows Overexpression of Nuclear Survivin and Low COX-2 Expression" 대한병리학회 46 (46): 55-60, 2012

      23 Paunovic I, "Combined immunohistochemistry for thyroid peroxidase, galectin-3, CK19and HBME-1 in differential diagnosis of thyroid tumors" 120 : 368-379, 2012

      24 Cerutti JM, "A preoperative diagnostic test that distinguishes benign from malignant thyroid carcinoma based on gene expression" 113 : 1234-1242, 2004

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      외국어명 : The Korean Journal of Pathology -> Journal of Pathology and Translational Medicine
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      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-04-13 학술지명변경 한글명 : 대한병리학회지 -> The Korean Journal of Pathology KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.13 0.13 0.12
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.13 0.11 0.409 0.01
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