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在人类口腔肿瘤发生的连续渐进阶段中,桥粒黏附在蛋白质和超微结构水平上的改变。

Alterations in desmosomal adhesion at protein and ultrastructure levels during the sequential progressive grades of human oral tumorigenesis.

作者信息

Sawant Sharada, Dongre Harsh, Ahire Chetan, Sharma Shilpi, Jamghare Sayli, Kansara Yashvi, Rane Pallavi, Kanojia Deepak, Patil Asawari, Chaukar Devendra, Gupta Sudeep, D'Cruz Anil, Vaidya Milind, Dongre Prabhakar

机构信息

Vaidya Laboratory, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Centre, Kharghar, Navi Mumbai, Maharashtra, India.

Department of Clinical Medicine and Centre for Cancer Biomarkers, Haukeland University Hospital, University of Bergen, Bergen, Norway.

出版信息

Eur J Oral Sci. 2018 Aug;126(4):251-262. doi: 10.1111/eos.12426. Epub 2018 Jun 15.

Abstract

With the aim of developing early diagnostic/prognostic markers for oral cancer, desmosomal adhesion in sequentially progressive grades of tissues from oral normal/disorders (normal, hyperplastic, dysplastic, non-metastatic/metastatic tumours, and metastatic nodes) was investigated at protein and ultrastructural levels using immunohistochemistry and transmission electron microscopy, respectively. The expression of desmosomal proteins was higher in hyperplastic tissues than in normal tissues but was significantly decreased in subsequent progressive stages of the disease. Altered expression of desmosomal proteins was significantly correlated with local recurrence and disease-free survival. Ultrastructural analysis in the corresponding tissues revealed cytoplasmic clustering of desmosomes in hyperplasia; in more advanced disease stages, a significantly lower number of desmosomes and widened intercellular spaces were observed. Altered protein expression resulting in structural changes was confirmed by knocking down desmoplakin expression in non-transformed cells, which failed to form normal desmosome structures and induced a cell-transformation phenotype. Our data suggest that alterations in desmosomal assembly initiate at an early hyperplastic grade and, with more advanced disease stages, the severity of the alterations gradually becomes higher. Alterations in desmosomal adhesion can be useful for early detection of high-risk premalignant lesions, as well as for identification of invasive characteristics of primary non-metastatic tumours. Early detection will help to control further progression of disease by timely intervention.

摘要

为了开发口腔癌的早期诊断/预后标志物,分别使用免疫组织化学和透射电子显微镜在蛋白质和超微结构水平上研究了口腔正常/疾病(正常、增生、发育异常、非转移性/转移性肿瘤和转移淋巴结)的连续进展组织分级中的桥粒黏附。桥粒蛋白在增生组织中的表达高于正常组织,但在疾病随后的进展阶段显著降低。桥粒蛋白表达的改变与局部复发和无病生存期显著相关。相应组织的超微结构分析显示增生组织中桥粒的细胞质聚集;在更晚期的疾病阶段,观察到桥粒数量显著减少且细胞间隙增宽。通过敲低未转化细胞中的桥粒斑蛋白表达证实了导致结构变化的蛋白质表达改变,未转化细胞无法形成正常的桥粒结构并诱导细胞转化表型。我们的数据表明,桥粒组装的改变在增生早期阶段就已开始,并且随着疾病阶段的进展,改变的严重程度逐渐升高。桥粒黏附的改变可用于早期检测高危癌前病变,以及识别原发性非转移性肿瘤的侵袭特征。早期检测将有助于通过及时干预控制疾病的进一步进展。

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