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癌胚抗原在表达碳水化合物抗原的结肠癌细胞进展中的作用。

Role of carcinoembryonic antigen in the progression of colon cancer cells that express carbohydrate antigen.

作者信息

Minami S, Furui J, Kanematsu T

机构信息

Department of Surgery II, Nagasaki University School of Medicine, Japan.

出版信息

Cancer Res. 2001 Mar 15;61(6):2732-5.

Abstract

Carcinoembryonic antigen (CEA) has been reported to promote the metastatic potential in some experimental tumors. Adhesion molecules are known to play an important role in the process of metastasis. Cytokines, including interleukin 1beta (IL-1beta) and tumor necrosis factor-alpha (TNF-alpha), which are produced by Kupffer cells, induce endothelial cells to express adhesion molecules. As a result, the present study was designed to investigate whether the interaction between CEA and Kupffer cells accelerated the metastatic potential of tumors in the liver. Kupffer cells isolated from the liver of male BALB/c mice were cultured with CEA, either with or without the addition of a cytokine inhibitor. The levels of IL-1beta and TNF-alpha were examined in a culture medium. An adhesion assay of colon cancer cell lines to human umbilical vein endothelial cells was also performed. When CEA was added to the Kupffer cell culture medium, cytokines were produced. Elevated levels of cytokines appeared to lead to increased rates of adhesion of cancer cells to endothelial cells. However, these phenomena were blocked by the addition of cytokine inhibitors. CEA stimulated Kupffer cells to produce cytokines. An elevated number of cytokines have been proven to promote the expression of adhesion molecules in endothelial cells. These processes are therefore considered to contribute to the metastasis of malignant cells to the liver. These results suggest that cytokine inhibitors may therefore play an important role in the inhibition of hepatic metastasis.

摘要

癌胚抗原(CEA)据报道可在一些实验性肿瘤中促进转移潜能。已知黏附分子在转移过程中起重要作用。包括库普弗细胞产生的白细胞介素1β(IL-1β)和肿瘤坏死因子-α(TNF-α)在内的细胞因子可诱导内皮细胞表达黏附分子。因此,本研究旨在调查CEA与库普弗细胞之间的相互作用是否会加速肿瘤在肝脏中的转移潜能。从雄性BALB/c小鼠肝脏分离的库普弗细胞与CEA一起培养,添加或不添加细胞因子抑制剂。检测培养基中IL-1β和TNF-α的水平。还进行了结肠癌细胞系与人脐静脉内皮细胞的黏附试验。当将CEA添加到库普弗细胞培养基中时,会产生细胞因子。细胞因子水平升高似乎导致癌细胞与内皮细胞的黏附率增加。然而,添加细胞因子抑制剂可阻断这些现象。CEA刺激库普弗细胞产生细胞因子。已证实细胞因子数量增加可促进内皮细胞中黏附分子的表达。因此,这些过程被认为有助于恶性细胞转移至肝脏。这些结果表明,细胞因子抑制剂可能在抑制肝转移中起重要作用。

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