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首页> 外文期刊>Pathology Research and Practice >Prognostic value of putative cancer stem cell markers (CD24, CD44, CD133, and ALDH1) in human papillary thyroid carcinoma
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Prognostic value of putative cancer stem cell markers (CD24, CD44, CD133, and ALDH1) in human papillary thyroid carcinoma

机译:预备癌症干细胞标志物(CD24,CD44,CD133和ALDH1)在人乳头状甲状腺癌中的预后价值

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We hypothesized that cancer stem cells (CSCs) are responsible for the poor outcome and aggressive clinicopathological factors. We surveyed the expression of selected CSC markers that are specifically expressed in thyroid papillary carcinoma (PTC). A total of 80 patients with PTC from 2011 to 2012 were enrolled. We selected CD24, CD44, CD133, and dehydrogenase 1 (ALDHI), as they have been suggested to be candidate CSC markers. Expression of these markers was investigated by immunohistochemical (IHC) staining. IHC staining for CD24, CD44, CD133 and ALDHI was evaluated according to staining intensity and proportion. The intensity and proportion scores were multiplied together for a total score, which was either 0-2 (negative) or 3-7 (positive). IHC for CD133 in PTC was positive in 49 (61.3%) patients, and CD24 was positive in 28 (35.0%). Seventy-eight (97.5%) patients were CD44 positive and 79 (98.8%) were ALDH1 positive. When we assessed the relationship between CSC markers and clinicopathological factors in PTC, CD24 expression was inversely correlated with multifocality (p = 0.045; odds ratio [OR], 0.370; 95% confidence interval [CI], 0.138-0.991) and CD44 expression was significantly correlated with a BRAF mutation (p=0.001; OR, 7.091; 95% CI, 4.101-12.262). However, CD133 and ALDH1 were not associated with any of the clinicopathological parameters. CD24 expression was inversely correlated with multifocality, and CD44 expression was significantly correlated with a BRAF mutation. Therefore, CD24 and CD44 are related to clinicopathological aggressive features and important for determining surgical extent in patients with PTC. (C) 2017 Elsevier GmbH. All rights reserved.
机译:我们假设癌症干细胞(CSCs)负责差的结果和侵袭性临床病理因素。我们调查了在甲状腺乳头状癌(PTC)中特异性表达的所选CSC标记的表达。 2011年至2012年共有80名患有PTC患者。我们选择了CD24,CD44,CD133和脱氢酶1(ALDHI),因为已经提出了候选CSC标记。通过免疫组织化学(IHC)染色研究了这些标志物的表达。根据染色强度和比例评价CD24,CD44,CD133和ALDHI的IHC染色。强度和比例分数乘以总分数,其为0-2(阴性)或3-7(阳性)。在49例(61.3%)患者中,PTC中CD133的IHC为阳性,CD24为阳性28(35.0%)。七十八(97.5%)患者的CD44阳性,79(98.8%)是Aldh1阳性。当我们评估PTC中CSC标记和临床病理因子之间的关系时,CD24表达与多致常数与多焦度相反(P = 0.045;差距[或],0.370; 95%置信区间[CI],0.138-0.991)和CD44表达是与BRAF突变显着相关(P = 0.001;或7.091; 95%CI,4.101-12.262)。然而,CD133和AlDH1与任何临床病理参数无关。 CD24表达与多焦度与多焦度相反,CD44表达与BRAF突变显着相关。因此,CD24和CD44与临床病理侵蚀性特征有关,并且对于在PTC患者中确定手术程度有关。 (c)2017 Elsevier GmbH。版权所有。

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