首页> 外文期刊>Pathology oncology research: POR >Clinical Significance of Hu-Antigen Receptor (HuR) and Cyclooxygenase-2 (COX-2) Expression in Human Malignant and Benign Thyroid Lesions
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Clinical Significance of Hu-Antigen Receptor (HuR) and Cyclooxygenase-2 (COX-2) Expression in Human Malignant and Benign Thyroid Lesions

机译:人类恶性和良性甲状腺病变中Hu抗原受体(HuR)和环氧合酶2(COX-2)表达的临床意义

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Hu-antigen R (HuR) is considered to play a crucial role in tumor formation and growth by binding to mRNAs encoding proteins such as Cyclooxygenase-2 (COX-2) and inducing their expression via mRNA stabilization and/or altered translation. The present study aimed to evaluate the clinical significance of HuR and COX-2 proteins' expression in human benign and malignant thyroid lesions. HuR and COX-2 proteins' expression was assessed immunohistochemically on paraffin-embedded thyroid tissues obtained from 98 patients with benign (n = 48) and malignant (n = 50) lesions and was statistically analyzed with clinicopathological parameters, follicular cells' proliferative capacity and recurrence risk rate. Enhanced HuR and COX-2 expression was significantly more frequently observed in malignant compared to benign thyroid lesions (p = 0.0073 and p = 0.0016, respectively), as well as in papillary carcinomas compared to hyperplastic nodules (p = 0.0039 and p = 0.0009, respectively). Positive associations of both HuR and COX-2 expression with follicular cells' proliferation rate were also noted (p = 0.0087 and p = 0.0127, respectively). In malignant thyroid lesions, elevated COX-2 expression was significantly associated with female patients' gender (p = 0.0381) and the presence of lymph node metastases (p = 0.0296). The present data support evidence that both HuR and COX-2 may be involved in the malignant state of thyroid neoplasia and may be utilized in the diagnosis of malignant thyroid tumors.
机译:人们认为,Hu抗原R(HuR)通过与编码诸如环氧合酶2(COX-2)的蛋白质的mRNA结合并通过mRNA稳定和/或改变的翻译来诱导其表达,从而在肿瘤的形成和生长中起关键作用。本研究旨在评估HuR和COX-2蛋白在人的甲状腺良恶性病变中的临床意义。在98例良性(n = 48)和恶性(n = 50)病变患者的石蜡包埋的甲状腺组织中对HuR和COX-2蛋白的表达进行了免疫组织化学评估,并通过临床病理学参数,滤泡细胞的增殖能力和复发风险率。与良性甲状腺病变相比(分别为p = 0.0073和p = 0.0016),在恶性肿瘤中以及在乳头状癌中与增生性结节(p = 0.0039和p = 0.0009)相比,HuR和COX-2表达的增强更为明显。分别)。还注意到HuR和COX-2表达与卵泡细胞的增殖率呈正相关(分别为p = 0.0087和p = 0.0127)。在甲状腺恶性病变中,COX-2表达升高与女性患者的性别(p = 0.0381)和淋巴结转移(p = 0.0296)显着相关。目前的数据支持的证据表明,HuR和COX-2都可能参与甲状腺肿瘤的恶性状态,并且可以用于诊断甲状腺恶性肿瘤。

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