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通过明氏分类法建立并鉴定一种增殖型胃癌细胞系。

Establishment and characterization of an expanding-type gastric cancer cell line by Ming's classification.

作者信息

Xu Hao, Peng Ji-Gui, Zhuang Yi-Fan, Chen Jia-Jia, Luo Qi-Cong, Huang Wei-Feng, Lin Chun-Dong, Cai Jian-Chun

机构信息

Department of Gastrointestinal Surgery, Zhongshan Hospital of Xiamen University, Xiamen, Fujian 361005, P.R. China.

Institute of Gastrointestinal Oncology, Medical College of Xiamen University, Xiamen, Fujian 361005, P.R. China.

出版信息

Oncol Rep. 2016 Nov;36(5):3030-3036. doi: 10.3892/or.2016.5090. Epub 2016 Sep 14.

Abstract

According to Ming's classification, gastric cancer (GC) can be divided into two types: expanding and infiltrative. The two types are readily recognizable by histology: expanding carcinomas grow en masse and by expansion, resulting in the formation of discrete tumour nodules, whereas in infiltrative carcinoma, tumour cells invade individually. Both types show varying degrees of cell maturation. The two types of carcinomas have vastly different pathological and clinical features. However, little is known concerning the mechanisms underlying these differences since no GC cell line models are available. For comprehensive and insightful analyses of mechanisms and treatment methods, new cell lines derived from expanding- and infiltrative-type gastric tumours are urgently needed. In the present study, we established an expanding-type GC cell line from a 72-year-old male patient. Different in vitro and in vivo methods were used to characterize the phenotypes of this cell line. This GC cell line was named XGC-2 and had an ~60 h doubling time. The cell line displayed strong colony formation and tumourigenicity in nude mice and had complicated chromosomal abnormalities. XGC-2 cells showed some markers of epithelial-to-mesenchymal transition (EMT), with decreased E-cadherin expression levels and increased vimentin expression levels. The XGC-2 cell line may be useful for future studies of GC development, progression, metastasis and therapy.

摘要

根据明氏分类法,胃癌(GC)可分为两种类型:膨胀型和浸润型。这两种类型通过组织学很容易识别:膨胀型癌整体生长并通过扩张形成离散的肿瘤结节,而浸润型癌中肿瘤细胞单个浸润。两种类型均表现出不同程度的细胞成熟。这两种类型的癌具有截然不同的病理和临床特征。然而,由于没有可用的胃癌细胞系模型,关于这些差异背后的机制知之甚少。为了对机制和治疗方法进行全面而有见地的分析,迫切需要从膨胀型和浸润型胃肿瘤中获得新的细胞系。在本研究中,我们从一名72岁男性患者中建立了一种膨胀型胃癌细胞系。使用不同的体外和体内方法来表征该细胞系的表型。该胃癌细胞系命名为XGC-2,倍增时间约为60小时。该细胞系在裸鼠中表现出强大的集落形成能力和致瘤性,并且具有复杂的染色体异常。XGC-2细胞显示出一些上皮-间质转化(EMT)的标志物,E-钙黏蛋白表达水平降低而波形蛋白表达水平升高。XGC-2细胞系可能对未来胃癌的发生、发展、转移和治疗研究有用。

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