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缝隙连接蛋白 connexin43 在 4-硝基喹啉-1-氧化物诱导的大鼠舌癌发生过程中的表达。

Expression of gap junctional protein connexin43 during 4-nitroquinoline-1-oxide-induced rat tongue carcinogenesis.

机构信息

Department of Oral Medicine, Guanghua School of Stomatology and Institute of Stomatological Research, Sun Yat-Sen University,Guangzhou, Guangdong, People's Republic of China.

出版信息

J Mol Histol. 2009 Jun;40(3):183-8. doi: 10.1007/s10735-009-9229-y. Epub 2009 Sep 26.

Abstract

Oral carcinogenesis is a multistep process and requires accumulation and interplay of a series of molecular genetic events. Gap junctions are intercellular channels composed of connexin subunits that mediate cell-cell communication. The disfunctions of gap junctions are believed to be associated with cancer development. We therefore investigated the expression of connexin (Cx)43, one of the major connexins in oral epithelia, during 4-nitroquinoline-1-oxide-induced rat tongue carcinogenesis. By immunohistochemistry, Cx43 expression was observed mainly in the cell membrane in normal rat oral epithelia. It was weak in the basal cell layer, increased in the stratum spinosum and stratum granulosum, and negative in the stratum corneum of normal epithelia. Throughout the course of carcinogenesis, both Cx43 immunostained area and mean intensity decreased with significant difference among various histopathological groups (P < 0.05). In cancerous oral epithelia cytoplasmic staining could be observed. However, Cx43 mRNA level showed no significant difference in the progress of oral carcinogenesis (P > 0.05) and without correlation to Cx43 protein immunostained area and mean intensity. Our results indicated that downregulation of Cx43 might be an early event during oral carcinogenesis, which could be a biomarker for early changes in oral malignant transformation.

摘要

口腔癌发生是一个多步骤的过程,需要一系列分子遗传学事件的积累和相互作用。缝隙连接是由连接子亚基组成的细胞间通道,介导细胞间通讯。缝隙连接功能障碍与癌症的发生有关。因此,我们研究了缝隙连接蛋白(Cx)43在 4-硝基喹啉-1-氧化物诱导的大鼠舌癌发生过程中的表达。通过免疫组织化学,在正常大鼠口腔上皮中主要观察到 Cx43 表达在细胞膜上。在基底细胞层较弱,棘层和颗粒层增加,正常上皮的角质层阴性。在癌变过程中,Cx43 免疫染色面积和平均强度均随各组织病理学组的不同而显著降低(P <0.05)。在癌变的口腔上皮中可观察到细胞质染色。然而,在口腔癌发生过程中 Cx43mRNA 水平没有显著差异(P >0.05),与 Cx43 蛋白免疫染色面积和平均强度没有相关性。我们的结果表明,Cx43 的下调可能是口腔癌变早期的一个事件,可能是口腔恶性转化早期变化的生物标志物。

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