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首页> 外文期刊>Pathology oncology research: POR >Ultrasound Risk Assessment Combined with Molecular Markers of Galectin-3, c-MET, HBME-1 and CK19 for Diagnosis of Malignant and Benign Thyroid Nodules
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Ultrasound Risk Assessment Combined with Molecular Markers of Galectin-3, c-MET, HBME-1 and CK19 for Diagnosis of Malignant and Benign Thyroid Nodules

机译:超声风险评估结合Galectin-3,C-Met,HBME-1和CK19的分子标记,用于诊断恶性和良性甲状腺结节

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摘要

To investigate the effect of ultrasound combined with expression of Galectin-3, c-Met, HBME-1 and CK19 in differentiating malignant from benign thyroid nodules. Forty-six patients with thyroid nodules were studied with ultrasound and immunohistochemical staining of excised thyroid nodules. The data were classified and compared. The immunohistochemical staining revealed 8 benign and 41 malignant thyroid lesions. In ultrasound risk assessment, the malignancy risk was low in four nodules, medium in five and high in 37 with lymphatic metastasis in 26. A significant (P 0.05) association existed in the expression of Galectin-3 with nodule boundary and lymphatic metastasis, in HBME-1 with nodule micro-calcification and in c-Met with nodule micro-calcification and lymphatic metastasis. CK19 expression was not significantly (P 0.05) associated with any of ultrasound features of nodule. Galectin-3, c-Met, HBME-1 and CK19 were significantly (P 0.05) different in malignant and benign thyroid lesions, with a significant (P 0.01) tendency in all the molecular markers in predicting the malignant from benign lesions. The ultrasound characteristics could significantly (P 0.001) predict malignant nodules with a significant (P 0.05) prediction tendency. The scores of Galectin-3, c-Met and CK19 significantly (P 0.05) increased with increase of ultrasound malignancy risk degree. In malignant and benign lesions differentiated by ultrasound, no significant (P 0.05) difference existed in HBME-1 expression, however, with ultrasound malignancy risk increase, the score of HBME-1 expression increased significantly (P = 0.03). Galectin-3, c-Met, HBME-1 and CK19 have significantly greater expressions in thyroid malignant than benign lesions and their expression increases with increase of ultrasound malignancy risk. The combination of both ultrasound and molecular markers can be used to differentiate malignant and benign thyroid lesions.
机译:为了探讨超声结合的效果与Galectin-3,C-Met,HBME-1和CK19的表达鉴定来自良性甲状腺结节的恶性肿瘤。用超声和免疫组化的切除甲状腺结节进行研究,研究了四十六名甲状腺结节患者。数据分类并进行比较。免疫组织化学染色显示出8良性和41个恶性甲状腺病变。在超声风险评估中,在26例中,4种结节中的4个结节,5分钟和高37中的培养基中含有淋巴结转移,存在显着(P <0.05)的关联,其在结节边界和淋巴结转移中存在显着(P <0.05)个关联。在HBME-1中,具有结节微钙化和C-Met中的结节微钙化和淋巴结转移。 CK19表达未显着(p> 0.05)与结节的任何超声特征相关。在恶性和良性甲状腺病变中有显着(p <0.05)的Galectin-3,C-Met,HBME-1和CK19,在所有分子标记中预测来自良性病变的恶性肿瘤的所有分子标记有显着(P <0.01)趋势。超声特性可显着(p <0.001)预测具有显着(P <0.05)预测趋势的恶性结节。随着超声恶性风险程度的增加,Galectin-3,C-Met和CK19的评分显着增加(P <0.05)。在通过超声分化的恶性和良性病变中,HBME-1表达中不存在显着(P> 0.05)差异,然而,随着超声恶性风险的增加,HBME-1表达的得分显着增加(P = 0.03)。 Galectin-3,C-Met,HBME-1和CK19在甲状腺恶性肿瘤中具有显着更大的表达,而不是良性病变,并且它们的表达随着超声恶性风险的增加而增加。超声和分子标记的组合可用于区分恶性和良性甲状腺病变。

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