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细胞周期蛋白D1的表达与口腔鳞状细胞癌中的细胞分化和细胞增殖相关。

Cyclin D1 expression is correlated with cell differentiation and cell proliferation in oral squamous cell carcinomas.

作者信息

Ohnishi Yuichi, Watanabe Masahiro, Wato Masahiro, Tanaka Akio, Kakudo Kenji, Nozaki Masami

机构信息

Second Department of Oral and Maxillofacial Surgery, Osaka Dental University, Hirakata, Osaka 573-1121, Japan.

Department of Oral Pathology, Osaka Dental University, Hirakata, Osaka 573-1121, Japan.

出版信息

Oncol Lett. 2014 Apr;7(4):1123-1127. doi: 10.3892/ol.2014.1880. Epub 2014 Feb 13.

Abstract

The present study conducted an immunohistochemical investigation of cyclin D1 and Ki-67 expression in oral squamous cell carcinoma (SCC) to evaluate the correlations between cell differentiation, cell proliferation and metastasis, and the effect of anticancer drug medication and cyclin D1 expression. Cyclin D1 and Ki-67 were detected clearly in the nuclei of 35 SCC samples. No correlation between cyclin D1 protein expression and oral SCC differentiation was found. By contrast, the majority of metastatic foci (90%) exhibited strong cyclin D1 expression, whereas weak expression was observed in metastatic foci with pre-operative adjuvant therapy. Additionally, cyclin D1 and Ki-67 were expressed in basal to suprabasal cells of well-differentiated oral SCC, whereas cyclin D1-positive and Ki-67-negative cells were present in the highly-differentiated region, according to a double-immunostaining method. These results indicate that the expression of cyclin D1 protein plays a role in cell differentiation and cell proliferation in well-differentiated oral SCC.

摘要

本研究对口腔鳞状细胞癌(SCC)中细胞周期蛋白D1和Ki-67的表达进行了免疫组织化学研究,以评估细胞分化、细胞增殖与转移之间的相关性,以及抗癌药物治疗与细胞周期蛋白D1表达的影响。在35例SCC样本的细胞核中清晰检测到细胞周期蛋白D1和Ki-67。未发现细胞周期蛋白D1蛋白表达与口腔SCC分化之间存在相关性。相比之下,大多数转移灶(90%)表现出强烈的细胞周期蛋白D1表达,而术前辅助治疗的转移灶中观察到弱表达。此外,根据双重免疫染色方法,细胞周期蛋白D1和Ki-67在高分化口腔SCC的基底至上基底细胞中表达,而在高分化区域存在细胞周期蛋白D1阳性和Ki-67阴性细胞。这些结果表明,细胞周期蛋白D1蛋白的表达在高分化口腔SCC的细胞分化和细胞增殖中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c4b/3961451/f3d40b9df00d/OL-07-04-1123-g00.jpg

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