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Identification of Trop-2 as an oncogene and an attractive therapeutic target in colon cancers.

机译:将Trop-2鉴定为结肠癌中的致癌基因和有吸引力的治疗靶标。

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摘要

The cell surface protein Trop-2 is highly expressed in a wide variety of epithelial cancers. In contrast, there is little or no expression of Trop-2 in adult somatic tissue. Because it is a cell surface protein that is selectively expressed in tumor cells, Trop-2 is a potential therapeutic target. However, whether Trop-2 is actively involved in tumorigenesis and whether its targeting for treatment would be effective have not been examined. Here, we show that Trop-2 expression is necessary for tumorigenesis and invasiveness of colon cancer cells, as both are inhibited when Trop-2 expression is suppressed by RNA interference. Conversely, ectopic expression of Trop-2 in colon cancer cells enhances their capacity for anchorage-independent growth and ectopic expression of Trop-2 in NIH3T3 cells is sufficient to promote both anchorage-independent growth and tumorigenesis. Importantly, we show that an antibody against the extracellular domain of Trop-2 reduces tumor cell invasiveness. Therefore, we have identified Trop-2 as an oncogene that has potential as a therapeutic target. Given the restricted expression of Trop-2 in normal tissue, anti-Trop-2 therapeutics would be predicted to have limited toxicity.
机译:细胞表面蛋白Trop-2在多种上皮癌中高度表达。相反,在成人体细胞组织中很少或没有Trop-2表达。因为Trop-2是在肿瘤细胞中选择性表达的细胞表面蛋白,所以它是潜在的治疗靶标。然而,尚未研究Trop-2是否积极参与肿瘤发生及其靶向治疗是否有效。在这里,我们显示Trop-2表达对于结肠癌细胞的肿瘤发生和侵袭是必要的,因为当RNA干扰抑制Trop-2表达时,两者都会被抑制。相反,Trop-2异位表达在结肠癌细胞中增强了其对锚定非依赖性生长的能力,而Trop-2异位表达在NIH3T3细胞中足以促进锚定非依赖性生长和肿瘤发生。重要的是,我们表明针对Trop-2胞外域的抗体可降低肿瘤细胞的侵袭性。因此,我们已将Trop-2确定为可能作为治疗靶标的致癌基因。由于Trop-2在正常组织中的表达受到限制,因此抗Trop-2治疗药物的毒性有限。

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