Department of Surgery, Division of Colon and Rectal Surgery, Penn State Milton S. Hershey Medical Center, Pennsylvania State University College of Medicine, 500 University Drive, Hershey, PA 17033, USA.
Dig Dis Sci. 2010 Nov;55(11):3171-80. doi: 10.1007/s10620-010-1138-0. Epub 2010 Feb 18.
Nkx2-3 has been reported to be up-regulated in B cell lines and intestinal tissues from Crohn's disease patients and down-regulated in colorectal cancer.
The purpose of the current study is to determine genes regulated by Nkx2-3 in sporadic (CRS61) and inflammatory bowel disease-associated (CRS4) colorectal cancer cell lines.
Small interfering RNA-mediated knockdown of Nkx2-3 in both cell lines was generated and high-density cDNA microarrays representing over 25,000 genes were performed. Microarray results were validated by RT-PCR and immunofluorescence. Pathway analysis was used to identify gene networks associated with Nkx2-3 knockdown in these cell lines.
A total of 1,677 genes were regulated by Nkx2-3 in CRS4 cells; 1,375 genes were regulated by Nkx2-3 in CRS61 cells. Among those genes regulated by Nkx2-3, 254 genes were similarly regulated by Nkx2-3 knockdown in both cell lines; 159 genes were differentially regulated by Nkx2-3 knockdown between the two lines. Genes regulated by Nkx2-3 were grouped primarily within the following two functional categories: (1) immune and inflammatory response; and (2) cell proliferation, growth, and oncogenesis. Among the genes with similarly changed expression in the two cell lines, the top affected pathways included antigen presentation and cell-cell signaling. Among the genes with differentially changed expression between the two cell lines, ingenuity pathway analysis indicated that the top affected pathway included genes directly involved in Wnt signaling.
Nkx2-3 may contribute to the pathogenesis of IBD-associated CRC and sporadic CRC by regulating the Wnt signaling pathway.
已有报道称 Nkx2-3 在 B 细胞系和克罗恩病患者的肠道组织中上调,而在结直肠癌中下调。
本研究旨在确定 Nkx2-3 在散发性(CRS61)和炎症性肠病相关(CRS4)结直肠癌细胞系中调节的基因。
用小干扰 RNA 介导的 Nkx2-3 在这两种细胞系中的敲低,并进行代表超过 25000 个基因的高密度 cDNA 微阵列分析。通过 RT-PCR 和免疫荧光验证微阵列结果。通路分析用于鉴定与这些细胞系中 Nkx2-3 敲低相关的基因网络。
在 CRS4 细胞中,共有 1677 个基因受 Nkx2-3 调节;在 CRS61 细胞中,有 1375 个基因受 Nkx2-3 调节。在受 Nkx2-3 调节的基因中,有 254 个基因在两种细胞系中受 Nkx2-3 敲低的相似调节;有 159 个基因在两条线上受 Nkx2-3 敲低的差异调节。受 Nkx2-3 调节的基因主要分为以下两个功能类别:(1)免疫和炎症反应;(2)细胞增殖、生长和肿瘤发生。在两种细胞系中表达相似变化的基因中,受影响最大的通路包括抗原呈递和细胞间信号传递。在两条线之间表达差异变化的基因中,通路分析表明,受影响最大的通路包括直接参与 Wnt 信号通路的基因。
Nkx2-3 可能通过调节 Wnt 信号通路,促进 IBD 相关 CRC 和散发性 CRC 的发病机制。