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甲状腺髓样癌中MiR-375和YAP1的表达谱及其与临床病理特征和预后的相关性

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

作者信息

Galuppini Francesca, Bertazza Loris, Barollo Susi, Cavedon Elisabetta, Rugge Massimo, Guzzardo Vincenza, Sacchi Diana, Watutantrige-Fernando Sara, Vianello Federica, Mian Caterina, Pennelli Gianmaria

机构信息

Department of Medicine (DIMED), Surgical Pathology Unit, University of Padova, Via Gabelli 61, 35121, Padova, Italy.

Department of Medicine (DIMED), Endocrinology Unit, University of Padova, Via Ospedale Civile 105, 35121, Padova, Italy.

出版信息

Virchows Arch. 2017 Nov;471(5):651-658. doi: 10.1007/s00428-017-2227-7. Epub 2017 Aug 31.

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.

摘要

甲状腺髓样癌(MTC)是一种生长缓慢的肿瘤,目前几乎没有可用的预后因素和治疗策略。最近的不同研究评估了分化良好的甲状腺癌的特征是不同微小RNA集的失调;然而,其中只有少数研究调查了miRNA表达在MTC中的作用。在本研究中,我们评估了130例MTC(104例为散发性,26例为家族性)中miR-375的表达,中位随访时间为39个月(范围1-138个月),然后将我们的结果与临床病理特征和患者预后相关联。此外,我们还评估了同一MTC系列以及5例C细胞增生(CCH)样本中YAP1(Yes相关蛋白1)的免疫组化表达。与正常甲状腺组织相比,我们观察到所有MTC中miR-375均显著上调。此外,发现miR-375表达与肿瘤大小、甲状腺包膜浸润机会、淋巴结转移风险和肿瘤分期密切相关。随访结束时,只有10%(13/130)出现肿瘤进展,并且发现较高的miR-375表达与较差的患者预后密切相关。相反,YAP1免疫组化表达在肿瘤中急剧下调,而在CCH中弱表达。我们的结果表明miR-375在MTC进展中起核心作用,因此,我们认为miR-375途径可能是新型MTC治疗策略的有效靶点。

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