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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Identification of a secretory protein c19orf10 activated in hepatocellular carcinoma.
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Identification of a secretory protein c19orf10 activated in hepatocellular carcinoma.

机译:鉴定在肝细胞癌中激活的分泌蛋白c19orf10。

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摘要

The identification of genes involved in tumor growth is crucial for the development of inventive anticancer treatments. Here, we have cloned a 17-kDa secretory protein encoded by c19orf10 from hepatocellular carcinoma (HCC) serial analysis of gene expression libraries. Gene expression analysis indicated that c19orf10 was overexpressed in approximately two-thirds of HCC tissues compared to the adjacent noncancerous liver tissues, and its expression was significantly positively correlated with that of alpha-fetoprotein (AFP). Overexpression of c19orf10 enhanced cell proliferation of AFP-negative HLE cells, whereas knockdown of c19orf10 inhibited cell proliferation of AFP-positive Hep3B and HuH7 cells along with G1 cell cycle arrest. Supplementation of recombinant c19orf10 protein in culture media enhanced cell proliferation in HLE cells, and this effect was abolished by the addition of antibodies developed against c19orf10. Intriguingly, c19orf10 could regulate cell proliferation through the activation of Akt/mitogen-activated protein kinase pathways. Taken together, these data suggest that c19orf10 might be one of the growth factors and potential molecular targets activated in HCC.
机译:鉴定涉及肿瘤生长的基因对于开发本发明的抗癌治疗至关重要。在这里,我们从基因表达库的肝细胞癌(HCC)序列分析中克隆了由c19orf10编码的17 kDa分泌蛋白。基因表达分析表明,与邻近的非癌性肝组织相比,c19orf10在大约三分之二的HCC组织中过表达,并且其表达与甲胎蛋白(AFP)呈显着正相关。 c19orf10的过表达增强了AFP阴性HLE细胞的细胞增殖,而敲低c19orf10则抑制了AFP阳性Hep3B和HuH7细胞的细胞增殖以及G1细胞周期停滞。在培养基中补充重组c19orf10蛋白可增强HLE细胞中的细胞增殖,并且通过添加针对c19orf10开发的抗体可消除这种作用。有趣的是,c19orf10可以通过激活Akt /丝裂原激活的蛋白激酶途径来调节细胞增殖。综上所述,这些数据表明c19orf10可能是HCC中激活的生长因子和潜在的分子靶标之一。

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