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MiR-375 and YAP1 expression profiling in medullary thyroid carcinoma and their correlation with clinical–pathological features and outcome

机译:miR-375和YAP1表达谱中髓质甲状腺癌及其与临床病理特征和结果的相关性

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Abstract Medullary thyroid cancer (MTC) is a tumor marked by an indolent growth for which few prognostic factors and therapeutic strategies are actually available. Different studies have recently appraised well-differentiated thyroid cancers are characterized by a dysregulation in different microRNA sets; however, only few of them investigated the role of miRNA expression in MTCs. In this study, we have assessed the miR-375 expression in a series of 130 MTCs (104 are sporadic and 26 familial) with a median follow-up of 39?months (range 1–138) and then we have correlated our results with the clinical–pathological features and the patients’ outcome. Moreover, we have appraised YAP1 (Yes-associated protein 1) immunohistochemical expression in the same MTC series and in 5 C-cells hyperplasia (CCH) samples as well. We observed a significant upregulation of miR-375 in all MTCs, when compared to the normal thyroid tissues. Besides, miR-375 expression was found to be closely linked to neoplastic size, a chance of thyroid capsule infiltration, the risk of lymph node metastasis, and the staging of the tumor. At the end of follow-up, only 10% (13/130) showed a tumor progression and a higher miR-375 expression was found to be closely linked to a worst patient’ outcome. On the contrary, YAP1 immunohistochemical expression was sharply downregulated in tumors, whereas it was weakly expressed in CCHs. Our results suggest miR-375 plays a central role in MTC progression and, therefore, we seek following the idea that miR-375 pathway may be an effective target in novel MTC therapeutic strategies.
机译:摘要髓质甲状腺癌(MTC)是一种由惰性生长标志着的肿瘤,其实际上是少数预后因素和治疗策略。最近评估了不同的研究良好分化的甲状腺癌的特征在于不同的MicroRNA套装中的缺点;然而,其中少数人在MTCS中只有很少的作用。在这项研究中,我们评估了一系列130 MTC(104个是零星和26家族)的MiR-375表达,其中中位随访39?月(范围1-138),然后我们与我们的结果相关联临床病理特征和患者的结果。此外,我们也在相同的MTC系列中和5个C细胞增生(CCH)样品中具有评估的YAP1(γ相关蛋白1)免疫组化表达。与正常的甲状腺组织相比,我们观察到所有MTCs中miR-375的显着上调。此外,发现miR-375表达与肿瘤尺寸紧密相关,甲状腺胶囊浸润的可能性,淋巴结转移的风险以及肿瘤的分期。在随访结束时,只有10%(13/130)显示肿瘤进展,发现更高的miR-375表达与最糟糕的患者的结果密切相关。相反,yap1免疫组织化学表达在肿瘤中急剧下调,而在CCH中弱食表达。我们的结果提出MiR-375在MTC进展中起着核心作用,因此我们寻求遵循MIR-375途径可能是新型MTC治疗策略中的有效目标。

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