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HOXB2是I期肺腺癌的不良预后指标,它通过对HOP-62非小细胞肺癌细胞中转移相关基因的转录调控来促进侵袭。

HOXB2, an adverse prognostic indicator for stage I lung adenocarcinomas, promotes invasion by transcriptional regulation of metastasis-related genes in HOP-62 non-small cell lung cancer cells.

作者信息

Inamura Kentaro, Togashi Yuki, Ninomiya Hironori, Shimoji Takashi, Noda Tetsuo, Ishikawa Yuichi

机构信息

Department of Pathology, The Cancer Institute, Japanese Foundation for Cancer Research (JFCR), Koto-ku, Tokyo, Japan.

出版信息

Anticancer Res. 2008 Jul-Aug;28(4B):2121-7.

Abstract

BACKGROUND

Previously, using microarray and real-time RT-PCR analysis, we established that HOXB2 is an adverse prognostic indicator for Stage I lung adenocarcinomas. HOXB2 is one of the homeobox master development-controlling genes regulating morphogenesis and cell differentiation.

MATERIALS AND METHODS

The molecular functions of HOXB2 were analyzed with a small interfering RNA (siRNA) approach in HOP-62 human non-small cell lung cancer (NSCLC) cells featuring high HOXB2 expression. Matrigel invasion assays and microarray gene expression analysis were compared between the HOXB2-siRNA cells and the control cells.

RESULTS

The Matrigel invasion assays showed attenuation of HOXB2 expression by siRNA to result in a significant decrease of invasiveness compared to the control cells (p = 0.0013, paired t-test). On microarray gene expression analysis, up-regulation of many metastasis-related genes and others correlating with HOXB2 expression was observed in the control case. With attenuation of HOXB2 expression, downregulation was noted for laminins alpha 4 and 5, involved in enriched signaling, and for Mac-2BP (Mac-2 binding protein) and integrin beta 4 amongst the genes having an enriched glycoprotein ontology.

CONCLUSION

HOXB2 promotes invasion of lung cancer cells through the regulation of metastasis-related genes.

摘要

背景

此前,通过微阵列和实时逆转录聚合酶链反应分析,我们确定HOXB2是I期肺腺癌的不良预后指标。HOXB2是调控形态发生和细胞分化的同源框主发育控制基因之一。

材料与方法

采用小干扰RNA(siRNA)方法,在高表达HOXB2的HOP-62人非小细胞肺癌(NSCLC)细胞中分析HOXB2的分子功能。比较HOXB2-siRNA细胞与对照细胞的基质胶侵袭试验和微阵列基因表达分析。

结果

基质胶侵袭试验显示,与对照细胞相比,siRNA介导的HOXB2表达减弱导致侵袭性显著降低(配对t检验,p = 0.0013)。在微阵列基因表达分析中,对照病例中观察到许多转移相关基因以及与HOXB2表达相关的其他基因上调。随着HOXB2表达减弱,在具有丰富糖蛋白本体的基因中,参与富集信号传导的层粘连蛋白α4和α5、Mac-2BP(Mac-2结合蛋白)和整合素β4下调。

结论

HOXB2通过调控转移相关基因促进肺癌细胞侵袭。

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