Inamura Kentaro, Togashi Yuki, Ninomiya Hironori, Shimoji Takashi, Noda Tetsuo, Ishikawa Yuichi
Department of Pathology, The Cancer Institute, Japanese Foundation for Cancer Research (JFCR), Koto-ku, Tokyo, Japan.
Anticancer Res. 2008 Jul-Aug;28(4B):2121-7.
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.
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.
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.
HOXB2 promotes invasion of lung cancer cells through the regulation of metastasis-related genes.
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。
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。
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。
HOXB2通过调控转移相关基因促进肺癌细胞侵袭。