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首页> 外文期刊>Oral oncology >Stromal myofibroblasts and malignant transformation in a 4NQO rat tongue carcinogenesis model.
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Stromal myofibroblasts and malignant transformation in a 4NQO rat tongue carcinogenesis model.

机译:4NQO大鼠舌癌发生模型中的间质成纤维细胞和恶性转化。

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This study assesses the correlation of changes in the density of stromal myofibroblasts to propagation of histopathologic alterations and proliferative activity of the epithelium in a rat 4NQO-induced tongue rat carcinogenesis model.Forty-three male Wistar rats were administered 0.001% 4NQO in drinking water for: 0 (n=7, control), 7 (n=4), 8 (n=8), 14 (n=6), 22 (n=9), and 28 (n=9) weeks, after which they were euthanized. Tongue sections were divided equally into anterior, middle and posterior thirds. Each third was given a histopathologic score (hematoxylin and eosin), ranging from normal, hyperplasia/hyperkeratosis, and escalating degrees of dysplasia to carcinoma, and analyzed by the point-counting method for density of epithelium-associated stromal myofibroblasts (alphaSMA) and of proliferating epithelial cells (PCNA). Histopathologic changes significantly increased in severity (carcinoma) with duration of 4NQO administration (p<0.001) in the posterior third of the tongue. The density of stromal myofibroblasts and proliferating epithelial cells was significantly higher in the posterior third of the tongue at 28 weeks compared to the other time points and locations (p<0.001, p=0.01, respectively). Significant correlations were found between occurrence of carcinoma and the increase in density of stromal myofibroblasts (p<0.001) and of proliferating epithelial cells (p=0.001) in the posterior third of the tongue. Increased density of stromal myofibroblasts was distinctively associated with the development of carcinoma but not with pre-malignant changes. Defining the mechanism of evolvement of carcinoma-associated stromal myofibroblasts is expected to further broaden our knowledge on the micro-environmental events occurring during the malignant transformation.
机译:本研究评估了大鼠4NQO致舌大鼠癌变模型中基质成纤维细胞密度变化与组织病理学改变的传播和上皮增殖活性的相关性.43只雄性Wistar大鼠在饮用水中给予0.001%的4NQO :0(n = 7,对照),7(n = 4),8(n = 8),14(n = 6),22(n = 9)和28(n = 9)周,之后被安乐死。舌头部分平均分为前三分之二。分别对三分之一的患者进行组织病理学评分(苏木精和曙红),范围从正常,增生/角化过度,不典型增生到癌变,并通过点计数法分析上皮相关的基质成肌纤维细胞(alphaSMA)和增殖上皮细胞(PCNA)。随着4NQO给药时间的延长,组织病理学改变的严重程度(癌)在舌后三分之一处增加(p <0.001)。与其他时间点和位置相比,在28周时,舌后三分之一处的间质成纤维细胞和增殖上皮细胞的密度显着更高(分别为p <0.001,p = 0.01)。在舌的后三分之一处,癌的发生与基质成肌纤维细胞密度的增加(p <0.001)和增殖上皮细胞的密度(p = 0.001)之间存在显着相关性。基质成肌纤维细胞密度的增加与癌的发展明显相关,但与恶变前的变化无关。定义癌症相关的基质成肌纤维细胞的进化机制有望进一步拓宽我们对恶性转化过程中发生的微环境事件的认识。

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