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DUSP4 /MKP2 overexpression is associated with BRAFV600E mutation and aggressive behavior of?papillary thyroid cancer

机译:DUSP4 / MKP2过表达与BRAF V600E 突变和甲状腺乳头状癌的侵袭行为有关

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The study was performed to retrospectively analyze the correlation of dual specificity phosphatase 4 ( DUSP4 ) expression with clinicopathological variables and BRAFV600E mutation to better characterize the potential role of DUSP4 as a biomarker in papillary thyroid cancer (PTC). Patients (n=120) who underwent surgery for PTC at Fudan University Shanghai Cancer Center (FUSCC) were enrolled in this study, and a validation cohort from The Cancer Genome Atlas (TCGA) database was identified to confirm the preliminary findings in our study. We investigated DUSP4 expression at the mRNA level in PTC tissues and adjacent normal tissues using real-time quantitative reverse transcription-polymerase chain reaction (qRT-PCR). BRAFV600E mutation analysis was also performed in PTC tissues using Sanger sequencing. Initially, we compared PTC tissues with paired normal tissues in DUSP4 expression using Student’s t -test, and then analyzed the correlation of DUSP4 with clinicopathological variables and BRAFV600E mutation in PTC using Mann–Whitney U , Kruskal–Wallis, χ 2, and Fisher’s exact tests. Human-derived thyroid cell lines were also used to verify our findings. DUSP4 was significantly overexpressed in PTC tissues compared with the adjacent normal tissues ( P V600E mutation in both the cohorts (FUSCC: P =0.002, TCGA: P V600E mutation-related.
机译:这项研究旨在回顾性分析双重特异性磷酸酶4(DUSP4)表达与临床病理变量和BRAF V600E 突变的相关性,以更好地表征DUSP4作为乳头状甲状腺癌(PTC)生物标志物的潜在作用。 。这项研究纳入了在复旦大学上海癌症中心(FUSCC)进行了PTC手术的患者(n = 120),并从癌症基因组图谱(TCGA)数据库中确定了一个验证队列,以证实我们研究的初步发现。我们使用实时定量逆转录聚合酶链反应(qRT-PCR)研究了PTC组织和邻近正常组织在mRNA水平上的DUSP4表达。还使用Sanger测序在PTC组织中进行了BRAF V600E 突变分析。最初,我们使用Student t检验比较PTC组织和成对的正常组织在DUSP4中的表达,然后使用Mann–Whitney U,Kruskal– Wallis,χ 2 和Fisher的精确检验。人类来源的甲状腺细胞系也被用来验证我们的发现。与相邻的正常组织相比,DUSP4在PTC组织中显着过表达(两个队列中的P V600E 突变(FUSCC:P = 0.002,TCGA:P V600E 突变相关)。

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