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Diagnostic value of MicroPure imaging for malignant thyroid nodule microcalcification and its correlation with the oncogene expression in nodules

机译:MicroPure成像对甲状腺恶性结节微钙化的诊断价值及其与结节中癌基因表达的相关性

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Objective: To study the diagnostic value of MicroPure imaging for malignant thyroid nodulemicrocalcification and its correlation with the oncogene expression in nodules. Methods:Patients with thyroid nodules confirmed by ultrasound in Dongtai People's Hospital betweenJune 2014 and October 2016 were selected and divided into those with malignant thyroidnodules and benign thyroid nodules according to the pathological results, and MicroPureimaging technology was used to judge the microcalcification and further divide the malignantthyroid nodules into microcalcification (+) and microcalcification (-). The biopsy tissuewas collected to detect the expression of cyclin, cell invasion molecules and angiogenesismolecules. Results: CyclinD1, CyclinE, MCM7, MMP2, MMP13, Vimentin, N-cadherin,Twist, HIF-1α, VEGF-C,VEGFR-2, VEGFR-3, Ang-2 and Tie-2 expression in malignantthyroid nodules of microcalcification (+) group and microcalcification (-) group weresignificantly higher than those of benign group while CyclinG2 and P53 expression weresignificantly lower than those of benign group; CyclinD1, CyclinE, MCM7, MMP2, MMP13,Vimentin, N-cadherin, Twist, HIF-1α, VEGF-C, VEGFR-2, VEGFR-3, Ang-2 and Tie-2expression in malignant thyroid nodules of microcalcification (+) group were significantlyhigher than those of microcalcification (-) group while CyclinG2 and P53 expression weresignificantly lower than those of microcalcification (-) group. Conclusion: Malignant thyroidnodule microcalcification detected by MicroPure imaging has a good correlation with cancercell proliferation, invasion and angiogenesis.
机译:目的:探讨MicroPure成像对甲状腺结节微钙化的诊断价值及其与结节中癌基因表达的相关性。方法:选择2014年6月至2016年10月在东台市人民医院经超声检查确诊的甲状腺结节患者,根据病理结果分为甲状腺恶性结节和甲状腺良性结节,采用微影像成像技术判断其微钙化程度,并进一步细分。甲状腺恶性结节分为微钙化(+)和微钙化(-)。收集活检组织以检测细胞周期蛋白,细胞侵袭分子和血管生成分子的表达。结果:CyclinD1,CyclinE,MCM7,MMP2,MMP13,波形蛋白,N-钙黏着蛋白,Twist,HIF-1α,VEGF-C,VEGFR-2,VEGFR-3,Ang-2和Tie-2在甲状腺微钙化结节中的表达( +)组和微钙化(-)组显着高于良性组,而CyclinG2和P53表达显着低于良性组; CyclinD1,CyclinE,MCM7,MMP2,MMP13,波形蛋白,N-钙黏着蛋白,Twist,HIF-1α,VEGF-C,VEGFR-2,VEGFR-3,Ang-2和Tie-2在恶性甲状腺结节的微钙化表达(+) CyclinG2和P53的表达明显低于微钙化(-)组,而微钙化(-)组明显高于微钙化(-)组。结论:MicroPure影像学检查发现的甲状腺恶性结节微钙化与癌细胞的增殖,侵袭和血管生成有良好的相关性。

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