首页> 外文期刊>Histochemistry and cell biology >Analysis of activated EGFR signalling pathways and their relation to laminin-5 gamma2 chain expression in oral squamous cell carcinoma (OSCC).
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Analysis of activated EGFR signalling pathways and their relation to laminin-5 gamma2 chain expression in oral squamous cell carcinoma (OSCC).

机译:口腔鳞状细胞癌(OSCC)中活化的EGFR信号通路及其与层粘连蛋白5 gamma2链表达的关系分析。

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Overexpression of epidermal growth factor receptor (EGFR) was shown for the majority of squamous cell carcinomas. The EGFR expression correlates to tumour size, stage and cytoplasmic accumulation of the laminin-5 gamma2 chain (Ln-5/gamma2), which is known as a marker of invading tumour cells. There is only limited knowledge if and how EGFR signalling pathways are important for invasion-associated processes and for the regulation of Ln-5/gamma2. Therefore the distribution of phosphorylated Erk1/2, p38 MAPK and Akt was immunohistochemically defined in oral squamous cell carcinoma (OSCC) of different histological grade and compared to histological criteria of invasion and cytoplasmic Ln-5/gamma2 deposition. With raising histological grade, there is a slight increase in nuclear pErk1/2-stained tumour cells (P=0.398) and a loss of nuclear (P=0.593) and increased cytoplasmic staining (P=0.144) of pAkt mainly in invading OSCC cells. Nuclear pp38 MAPK could only be sporadically detected in few cases. In case of pErk1/2 and pAkt, only a partial co-localisation could be revealed in cases with abundant kinases and Ln-5/gamma2. Among the investigated kinases, only pAkt shows a relation to histological grade and invasion in OSCC. pErk1/2, pp38 MAPK and pAkt do not represent a direct link between EGFR and Ln-5 synthesis. Therefore, enhanced Ln-5/gamma2 may be a secondary phenomenon of EGFR-induced tumour cell proliferation and dissemination.
机译:对于大多数鳞状细胞癌,表皮生长因子受体(EGFR)的过度表达。 EGFR的表达与层粘连蛋白5 gamma2链(Ln-5 / gamma2)的肿瘤大小,分期和细胞质积累相关,后者被称为入侵肿瘤细胞的标志物。 EGFR信号通路对于以及与入侵相关的过程以及对Ln-5 / gamma2的调控是否重要,只有很少的知识。因此,在不同组织学等级的口腔鳞状细胞癌(OSCC)中,免疫组织化学确定了磷酸化的Erk1 / 2,p38 MAPK和Akt的分布,并与浸润和细胞质Ln-5 /γ2沉积的组织学标准进行了比较。随着组织学等级的提高,主要在侵袭性OSCC细胞中,pErk1 / 2染色的肿瘤细胞略有增加(P = 0.398),pAkt的核丢失(P = 0.593)和细胞质染色增加(P = 0.144)。 。仅在少数情况下偶发地检测到核pp38 MAPK。对于pErk1 / 2和pAkt,在激酶和Ln-5 /γ2丰富的情况下,只能部分共定位。在所研究的激酶中,只有pAkt与OSCC的组织学分级和侵袭有关。 pErk1 / 2,pp38 MAPK和pAkt不代表EGFR与Ln-5合成之间的直接联系。因此,增强的Ln-5 / gamma2可能是EGFR诱导的肿瘤细胞增殖和扩散的继发现象。

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