文章摘要
Li Zheng,Min Zhao,Xiangyang Hu,Jin Huang,Ling Ang,Hongguang Hu,Qiang Zou,Jin Wang,Mingqiang Liu,Yang Zhao. Clinical significance of HBME-1, Galectin-3, and CK19 expression and the status of BRAF mutation in papillary thyroid carcinoma. Oncol Transl Med, 2016, 2: 174-178.
Galectin-3、CK19、HBME-1表达和BRAF突变在甲状腺乳头状癌中的意义
Clinical significance of HBME-1, Galectin-3, and CK19 expression and the status of BRAF mutation in papillary thyroid carcinoma
Received:February 13, 2016  Revised:July 23, 2016
DOI:10.1007/s10330-016-0145-9
中文关键词: 甲状腺乳头状癌; Galectin-3; CK19; HBME-1 ; BRAF
英文关键词: papillary thyroid carcinoma (PTC); human bone marrow endothelial cell markers (HBME-1); Galectin-3; cytokeratin19 (CK19); v-raf murine sarcoma viral oncogene homolog B1 (BRAF)
基金项目:
Author NameAffiliationE-mail
Li Zheng Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
Min Zhao* Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China Zhao.Min.hi@163.com 
Xiangyang Hu Department of Pathology, Anhui Medical University, Hefei 230032, China zhengli352@163.com 
Jin Huang Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
Ling Ang Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
Hongguang Hu Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
Qiang Zou Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
Jin Wang Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
Mingqiang Liu Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
Yang Zhao Department of Pathology, The Second People’s Hospital of Hefei, Hefei 230011, China zhengli352@163.com 
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中文摘要:
  摘要 目的 探讨半乳糖凝集素3(Galectin-3)、细胞角蛋白19(CK19)、人骨髓内皮细胞标记物(HBME-1)蛋白表达和鼠类肉瘤滤过性毒菌致癌同源体B1(BRAF)基因突变在甲状腺乳头状癌(PTC)中的意义 方法 采用免疫组化Envision法检测82例PTC和82例甲状腺良性病变中Galectin-3、CK19、HBME-1蛋白表达状况; 采用聚合酶链反应及DNA测序法检测60例PTC和60例甲状腺良性病变中BRAF基因突变状况。结果 ① 82例PTC中HBME-1 、Galectin-3和CK19的阳性表达率分别为98.8%、97.6%、100%,与良性病变比较,差异有统计学意义(P<0.05),而与临床病理参数间无相关性;另外联合检测3项蛋白指标,并以HBME-1联合 CK19或Galectin-3同时表达作为PTC诊断标准时,敏感度可高达99.9%,特异度达95.4% ;② 60例PTC中BRAF基因突变率为66.7%,与良性病变比较,差异有统计学意义(P<0.05),与临床病理参数间无相关性。结论 ① 蛋白标记物Galectin-3、CK19、HBME-1对PTC的诊断均有一定病理价值,其中以HBME-1最为理想,联合检测特异度敏感性更佳;② BRAF基因突变是PTC发生的一项重要事件,对其确诊可能具有价值。
英文摘要:
    Objective: The aim of this study was to explore the clinical significance of the expression of proteins human bone marrow endothelial cell markers (HBME-1), Galectin-3, and cytokeratin19 (CK19), as well as the status of v-raf murine sarcoma viral oncogene homolog B1 (BRAF) mutation in papillary thyroid carcinoma (PTC). Methods: Immunohistochemical staining was performed in 82 specimens each of PTC and papillary benign lesions to detect the expression of HBME-1, Galectin-3, and CK19. Polymerase chain reaction (PCR) and gene sequencing were performed on 60 specimens each of PTC and papillary benign lesions to detect the status of BRAF mutation. Results: The positive expression ratios of HBME-1, Galectin-3, and CK19 in PTC were 98.8%, 97.6% and 100% respectively, which were significantly higher than the expressions in papillary benign lesions (P < 0.05). No significant relationship was observed between the expression of these makers and the clinicopathological features of PTC. The sensitivity of co-expression of HBME-1 and CK19 or HBME-1 and Galectin-3 as diagnostic criteria of PTC was 99.9%, with a specificity of 95.4%. BRAF mutation was detected in 40 of 60 PTC (66.7%) specimens. There was a statistical difference in BRAF mutations between PTC and papillary benign lesions (P < 0.05); there were no associations between BRAF mutation and the clinicopathological features of PTC. Conclusion: Combined immunohistochemical staining of HBME-1, Galectin-3, and CK19 can further improve the sensitivity and specificity of differential diagnosis of PTC. BRAF mutation is a significant genetic event, which may have diagnostic value for PTC.
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