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Activation of nuclear factor-κB contributes to growth and aggressiveness of papillary thyroid carcinoma

机译:核因子-κB的活化有助于甲状腺乳头状癌的生长和侵袭性

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Nuclear factor-κB (NF-κB) is involved in proliferation, angiogenesis, and metastasis in various malignancies; however, the role of NF-κB in papillary thyroid carcinoma (PTC) has not been fully elucidated. The purpose of this study was to elucidate the role and clinicopathological significance of the NF-κB signaling pathway in PTC. We investigated NF-κB RelA expression in 122 patients with conventional PTC by immunohistochemistry, and evaluated the correlation between RelA expression and clinicopathological parameters, including BRAFV600E mutation. Nuclear expression of NF-κB RelA, regardless of cytoplasmic expression, was identified in 91 of 122 PTCs (74.6%), and was more frequent in PTCs larger than 1cm (overt PTC) (P=0.001). There were significant differences in clinicopathological parameters, such as extrathyroidal extension (P=0.031), nodal metastasis (P=0.021) and BRAFV600E mutation (P=0.039), between NF-κB-positive and negative PTCs. Proliferation index was strongly associated with NF-κB activation (P=0.045) but not with BRAFV600E mutation (P=0.141). Taken together, our results suggest that NF-κB RelA activation contributes, at least in part, to tumor growth and aggressiveness of PTC after tumor transformation. The expression pattern of NF-κB may serve as a prognostic marker and a potential therapeutic target.
机译:核因子κB(NF-κB)参与各种恶性肿瘤的增殖,血管生成和转移。然而,NF-κB在甲状腺乳头状癌(PTC)中的作用尚未完全阐明。这项研究的目的是阐明NF-κB信号通路在PTC中的作用和临床病理意义。我们通过免疫组织化学研究了122例常规PTC患者的NF-κBRelA表达,并评估了RelA表达与临床病理参数(包括BRAFV600E突变)之间的相关性。在122个PTC中,有91个(74.6%)鉴定出NF-κBRelA的核表达,而在1cm以上的PTC(显性PTC)中更为频繁(P = 0.001)。 NF-κB阳性和阴性PTCs在临床病理参数上有显着差异,例如甲状腺外扩展(P = 0.031),淋巴结转移(P = 0.021)和BRAFV600E突变(P = 0.039)。增殖指数与NF-κB激活密切相关(P = 0.045),而与BRAFV600E突变无关(P = 0.141)。两者合计,我们的结果表明,NF-κBRelA激活至少部分有助于肿瘤转化后的肿瘤生长和PTC的侵袭性。 NF-κB的表达模式可作为预后标志物和潜在的治疗靶标。

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