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首页> 外文期刊>Cancer investigation >Aberrant Level of Skp2 and p27KIP1 in Intraductal Proliferative Lesions is Associated with Tumorigenesis
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Aberrant Level of Skp2 and p27KIP1 in Intraductal Proliferative Lesions is Associated with Tumorigenesis

机译:管内增殖病变中的SKP2和P27KIP1的异常水平与肿瘤引发有关

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摘要

Breast cancer is one of the leading causes of cancer-related death in women worldwide. Here we aimed to examine the expression status of S-phase kinase-associated protein 2 (Skp2) and p27KIP1, and assess the significance of Skp2 plus p27KIP1 expression in patients with intraductal proliferative lesions, including ductal carcinoma in situ (DCIS) and atypical ductal hyperplasia (ADH). Skp2 and p27KIP1 mRNA levels in DCIS, ADH, flat epithelial atypia, and usual ductal hyperplasia (UDH) were evaluated by quantitative real-time reverse transcription polymerase chain reaction and protein expression was evaluated immunohistochemically in 60 fresh tissues and 120 paraffin-embedded tissues from patients with the four subtypes above. We found that the protein and mRNA level of Skp2 were significantly increased in DCIS and ADH as compared with that in UDH. In contrast, p27KIP1 protein and mRNA levels were reduced. Based on the above findings, abnormal levels of Skp2 and p27KIP1 have probably been involved in the pathogenesis of ADH and DCIS. Thus, Skp2 and p27KIP1 may serve as important diagnosis markers.
机译:乳腺癌是全球癌症相关死亡的主要原因之一。在这里,我们旨在检查S相激酶相关蛋白2(SKP2)和P27KIP1的表达状态,并评估SKP2加上P27KIP1表达在患有管内增殖病变患者中的意义,包括原位(DCIS)和非典型导管的导管癌增生(ADH)。通过定量实时逆转录聚合酶链反应评估DCIS,ADH,扁平上皮缺点和通常的导管增生(UDH)中的SKP2和P27KIP1 mRNA水平,并在60种新鲜组织中,从60种新鲜组织中免疫组织化学评估蛋白质表达和来自患者上述四种亚型。我们发现,与UDH相比,DCIS和ADH中SKP2的蛋白质和mRNA水平显着增加。相反,降低了p27kip1蛋白和mRNA水平。基于上述研究结果,SKP2和P27KIP1的异常可能参与了ADH和DCI的发病机制。因此,SKP2和P27KIP1可以用作重要的诊断标记。

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