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人胃癌中微小RNA - 143和 - 145表达降低。

Decreased expression of microRNA-143 and -145 in human gastric cancers.

作者信息

Takagi Takeshi, Iio Akio, Nakagawa Yoshihito, Naoe Tomoki, Tanigawa Nobuhiko, Akao Yukihiro

机构信息

Department of Medical Oncology, Gifu International Institute of Biotechnology, Kakamigahara, Japan.

出版信息

Oncology. 2009;77(1):12-21. doi: 10.1159/000218166. Epub 2009 May 12.

Abstract

OBJECTIVE

Downregulation of specific microRNAs (miRNAs) occurs in human tumors, which suggests a function for miRNAs in tumor suppression. We investigated the role of the miRNAs miR-143 and miR-145 in gastric cancers.

METHODS

The expression levels of miR-143 and miR-145 in the samples from 43 patients with gastric cancer were determined by real-time PCR using TaqMan assay. The growth inhibitory effect was estimated by the transfection of human gastric cancer cells with the miRNA.

RESULTS

The expression levels of miR-143 and -145 were decreased in most human gastric cancers examined, as previously reported to occur in colon tumors. The transfection of human gastric MKN-1 cells with miR-145 resulted in a greater growth inhibitory effect than that with miR-143, results which were contrary to those in colon cancers. In MKN-1 cells, an additive effect on growth inhibition was shown by the combined transfection with miR-143 and miR-145; further, higher sensitivity to 5-fluorouracil was also observed following the transfection with miR-143 or miR-145. The possible candidate target messenger RNAs of miR-145 were identified to be insulin receptor substrate-1 and beta-actin.

CONCLUSION

Taken together, these findings suggest that miR-143 and miR-145 act as anti-oncomirs common to gastrointestinal tumors.

摘要

目的

特定微小RNA(miRNA)在人类肿瘤中表达下调,提示miRNA具有肿瘤抑制功能。我们研究了miRNA-143和miRNA-145在胃癌中的作用。

方法

采用TaqMan法通过实时PCR测定43例胃癌患者样本中miR-143和miR-145的表达水平。通过用miRNA转染人胃癌细胞来评估其生长抑制作用。

结果

如先前报道在结肠肿瘤中出现的情况一样,在所检测的大多数人类胃癌中,miR-143和miR-145的表达水平降低。用miR-145转染人胃MKN-1细胞比用miR-143转染产生的生长抑制作用更强,这一结果与结肠癌中的情况相反。在MKN-1细胞中,miR-143和miR-145联合转染显示出对生长抑制的累加效应;此外,用miR-143或miR-145转染后还观察到对5-氟尿嘧啶的更高敏感性。已确定miR-145可能的候选靶信使核糖核酸为胰岛素受体底物-1和β-肌动蛋白。

结论

综上所述,这些发现表明miR-143和miR-145作为胃肠道肿瘤共有的抗癌miRNA发挥作用。

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