Rogers Carmelle D, Fukushima Noriyoshi, Sato Norihiro, Shi Chanjuan, Prasad Nijaguna, Hustinx Steven R, Matsubayashi Hiroyuki, Canto Marcia, Eshleman James R, Hruban Ralph H, Goggins Michael
Department of Pathology, The Sol Goldman Center for Pancreatic Cancer Research, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21231, USA.
Cancer Biol Ther. 2006 Oct;5(10):1383-9. doi: 10.4161/cbt.5.10.3323. Epub 2006 Oct 22.
The gene expression profile of pancreatic cancer is significantly different from that of normal pancreas. Differences in gene expression are detectable using microarrays, but microarrays have traditionally been applied to pancreatic cancer tissue obtained from surgical resection. We hypothesized that gene expression alterations indicative of pancreatic cancer can be detected by profiling the RNA of pancreatic juice.
We performed oligonucleotide microarray analysis on RNA isolated from pancreatic juice obtained endoscopically after secretin stimulation from six patients with pancreatic cancer and ten patients with nonneoplastic diseases of the pancreas or upper gastrointestinal tract. Extracted RNA was subjected to two rounds of linear RNA amplification, and then hybridized with U133A or X3P gene chips (Affymetrix).
Using the U133A or X3P chips, 37 and 133 gene fragments respectively, were identified as being at least 3-fold more abundant in the pancreatic juice of patients with pancreatic cancer compared to the noncancer controls (p<0.05, Mann-Whitney test). For example, pancreatic juice from patients with pancreatic cancer contained increased levels of IL8, IFITM1, fibrinogen, osteopontin, CXCR4, DAF and NNMT RNA, genes that have been previously reported as overexpressed in primary pancreatic cancers or pancreatic cancer cell lines relative to control tissues.
These results demonstrate that RNA analysis of pancreatic juice can reveal some of the same RNA alterations found in invasive pancreatic cancers. RNA analysis of pancreatic juice deserves further investigation to determine its utility as a tool for the evaluation of pancreatic lesions.
胰腺癌的基因表达谱与正常胰腺显著不同。使用微阵列可检测到基因表达的差异,但传统上微阵列已应用于手术切除获得的胰腺癌组织。我们推测,通过分析胰液RNA可检测到指示胰腺癌的基因表达改变。
我们对6例胰腺癌患者以及10例胰腺或上消化道非肿瘤性疾病患者在注射促胰液素后经内镜获取的胰液中分离出的RNA进行了寡核苷酸微阵列分析。提取的RNA进行两轮线性RNA扩增,然后与U133A或X3P基因芯片(Affymetrix)杂交。
使用U133A或X3P芯片,分别鉴定出37个和133个基因片段,与非癌症对照相比,这些基因片段在胰腺癌患者胰液中的丰度至少高3倍(p<0.05,曼-惠特尼检验)。例如,胰腺癌患者的胰液中IL8、IFITM1、纤维蛋白原、骨桥蛋白、CXCR4、DAF和NNMT RNA水平升高,这些基因先前已报道在原发性胰腺癌或胰腺癌细胞系中相对于对照组织过表达。
这些结果表明,胰液RNA分析可揭示侵袭性胰腺癌中发现的一些相同的RNA改变。胰液RNA分析值得进一步研究,以确定其作为评估胰腺病变工具的效用。